Well, hello.
**shy wave**
I'm intimidated by my own blog. It's with great trepidation, but also with inspiration, that I am hoping to revive La Vie.
There is so, so much to talk about, it can't all be done in one post and I think that's where some of my overwhelming desire to avoid my blog comes from. It's like the blanket I haven't finished crocheting. I don't really want to, but I know how happy I will feel if I just start working on it again. I like to crochet, as I like to write....and yet?
A good friend of mine once wrote the most beautiful passages on his blog and then one day he just stopped. He said he was tired of it, that everything just seemed so negative. While I begged to differ: I found his posts honest and haunting and meditative, I understand now that to be able to mix and match the words in an honest and haunting way you often have to feel a sense of that within your world, in the same way that gives form to your words. When you feel like shit, it gets hard. And my dear readers (I've another idea! The dedication of this blog...I'll come back to this), I have not been feeling too well.
The past year has been nutty: lots of changes in ole Shan, most not for the better. You might recall the collapsed lung (lobe), the many hospital stays, the oxygen, THE VENT, a short period sans oxygen post vent, and then kind of a dull and dreary but mostly boring late fall/winter. Things were boring in the sense that facebook wasn't going wild with pictures of me from my youth because a machine was breathing for me; in fact, I think I was only in the hospital once (?) post vent? But inside this little bod things were still a bit amok. It may just be that we had a good run, but Shanny's CF lungs (honestly, I cannot complain, they served me well) have had their day.
I used to write so openly about dying and fearing death and coming to grips with my self and my disease. I think I did a pretty good job of it all actually, but kinda it was a bunch of hogwash because I can tell you right now that when I was writing about death at 70% lung function it was all so esoteric and deep but what did I know about dying? What do I know about it now? I know with much more conviction that I am a lot closer to it. I know what it feels like to pass out from hypoxia, to have doctors say they don't know how else to help you, to have to plan your day strategically around walking and breathing and rest. But still. Still, inside, I still just feel like me. I don't feel that death is prowling around the place waiting. Should I? Will I? I expect that I would, but who knows? Think of how many people are here one minute and dead the next. You can't tell me they all saw it coming? Maybe they did though. Maybe it's not about seeing it but how long before it's upon you that you are aware of the dark sleep coming on? That I can believe, just as how in one year my life and lungs have changed so minutely to me that it seems so fast and yet such a logical progression both in the same time - like growing hair, if you will. However if you had not seen me for some time, perhaps you might be quite surprised in the changes?
I digress. What I want to say but haven't been able to spit out is that I am aware of the fact that I am in end stage lung disease and I admit that I am dying. Once I began to (and can I, really?) see that blur on the horizon not as the start of a new day or of some future plans to dream about but more as the point where I might not be here any more there came a shift in perspective. I can tell you with out a doubt that it is my love for my children that keeps me hanging on. I love my family, I love my husband, my friends. I know my death will upset them, sadden them. But I don't know that I think it would change them. Maybe I just am not able to see all the places I touch the world, that can be a hard thing for us to admit sometimes, but I do see it in my kids. I know that they need to have a mother in their lives, and I so very selfishly want it to be ME. As much as I fear I am fucking them up, that's MY job and I am not ready to quit. I am not ready to let some other woman do it, or their father alone, nor to place that job on my own parents. But I fear. I fear a lot. Letting go of fear is a huge challenge for me. I am not afraid of dying. I am pretty sure I can say that honestly now. I am afraid of leaving things undone.
I have so few ways I feel I can really touch the world, but my words are one way I have always felt capable.
We read so often about pain, struggle, uprising and the fact that there is a responsibility to some to simply bear witness. That's what I want to resurrection of this blog to be. Just to bear witness to what life was like for one sick mom who was trying to get it right for her kids and to leave this tiny legacy behind for them to have, just the words, thoughts, the silly beating heart of a girl who maybe didn't see it coming, but had been in a slow dance with it all the same; until it's time to change partners and bow this one out.
post script:
I can't leave here in good faith with that ending. The curtain ain't closed yet. So on Friday I head to Loyola Medical center in Maywood, IL to have an introductory meeting with the transplant pulmonologist. yipes! It doesn't mean that I have chosen TX nor does it mean that this transplant team has obliged to take me on. There are so, so many parts to this whole thing that have to come together before any decisions such as those are made. It DOES mean that I have said Yes, Yes, I will check this scary thing out and see. I am doing it for my kids, but I am lying if I say I haven't already climbed Everest at least once in my mind. You know, without supplemental oxygen ;)
They say, oh! What a tribulation...
All writing on this blog is copyright of Shannon North and can not be copied or reproduced without the author's consent.
Wednesday, February 26, 2014
Friday, May 24, 2013
twenty twenty twenty four hours to go... I wanna be sedated
I've been meaning to write my "story" about getting sick and all that went down at the beginning of the month but I have just been lazy. No, that's not entirely true, I have been on oxygen and IVs and doing ALL THE TREATMENTS and just pretty worn out at the end of the day with not much incentive to write.
So...I have to go back to the end of March to really begin. Maybe all the way back to November. In November I had this crazy pain in my right lung. It was almost intolerable though I did tolerate it for about 10 days because I knew I had a clinic visit coming up and I try not to do ANYTHING remotely CF related outside of my clinic because, for you non-CFers out there - the medical profession at large really knows very very little about CF and you wind up in a big cluster fuck of nonsense of you try to get anything accomplished without your CF team on board.
Anyway, I had an x-ray which demonstrated a right middle lobe atelectasis (basically it's like a collapsed lobe) and I had my first bronchoscopy. I think this was in November...maybe it was in January? I was definitely in the hospital in November and January (and March and April/May), though my timing might be off here. Either way, I ended up admitted again in January for the SAME infection.
My normal routine is to go into the hospital where I am desensitized to the antibiotics I need because I am allergic to them and then I finish up the course of abx at home. During my Jan admission I desatted during my sleep and required supplemental oxygen - which isn't weird for a sick CFer, but I didn't know it was going to be a thing.
Then it was March and I was sick, again. Once again, I put things off until I had my clinic appointment. I had my usual pulmonary function test and my FEV1 was 35%!! My baseline is about 55% so that's a significant dip. My doc ordered a CT, another bronch, and an admission for more IVs. The thing was, I had plans to go to CA the beginning of April that I wasn't willing to put off. Quality over quantity I rationalized. I did have the CT before I left.
CA wasn't that fun, simply because I felt like SHIT. I was so damn tired the entire time. I was almost relieved to be going to the hospital and I actually stayed for 4 days instead of my usual 24 hours. It was at this time that my need for continuous O2 was discovered. My oxygen sats actually went down to 77% at one point before I was put on 3L of O2. I was not taken off the O2 upon being released from the hospital and was told the only way I was going home was to go home with oxygen.
Wearing O2 and carrying a tank with you everywhere you go SUCKS. And it's pretty hard to convince your family that your OK when you have an oxygen cannula stuck to your face. So once I was realeased, I found myself resisting going places more and more. Which was OK because I really wasn't feeling well still. at.all.
My doc put me on an IV med called Meropenem, an inhaled med called Cayston, and an oral antibiotic called Zyvox. Zyvox is a nasty drug. It gave me terrible lethargy and the worst diarrhea of my life. I chalked feeling so poorly up to that medicine. As well, I found that if I wore the O2 at home and in the car, I really didn't feel THAT BAD if I took it off to run into the grocery store or the kids' schools. haha. little did I know.
So on Thursday, April 25th (I think), Miss M had a "Muffins for Moms" event at her school. I was there for about an hour and I left the O2 in the car.
I am going to back up a tiny bit to complain for a minute. My family were kind of dicks to me during this time. I asked for help a few times and mentioned more than once that I just wasn't feeling well and I was told to "step it up" and "quit complaining" by two of my family members. In their defense, I have spent the last 35 years pretending everything is fine, even when it hasn't been, so they really didn't know. But I mention that because 1) it comes into play about how I feel regarding fam later and 2) I was pushing myself really hard to feel that I accomplished something during the daytime rather than having to face everyone and say NO, I didn't do the laundry, NO I didn't make dinner, NO I haven't swept the floors. Retrospectively, who gives a fuck, right? But I felt guilty about doing nothing all day.
So, anyway, after "Muffins for Moms" I went home, stuck on the O2 and proceeded to watch a bunch of "Arrested Development" episodes. About 1 that afternoon a friend stopped by. This friend was a boy but not a romantic boy. Still, when the doorbell rang my vanity kicked in, and I locked up the dog, hung the O2 cannula on the doorknob and answered the door.
My friend knew I was on O2 and even said that he could see the indentations from the cannula and asked why I took it off. I shrugged and said, "No big deal, you will only be here for a few minutes anyway." We both noted how out of breath I was. I could not seem to catch my breath and I lamented how weird that was, as I had been wearing the oxygen all day and had only gotten up to answer the door.
I decided I needed the O2 after all and went into the other room to get the cannula. By the time I sat back down my dexterity seemed to be impeded and I could not get the cannula over my ears. Then I noticed my friend seemed to be going in slow motion. I said something was wrong. Then I started to pass out. It was like I was the drunkest I have ever been. I could not keep my head up or eyes open and I was trying to hold the O2 to my nose because I still could not get it on. I told him he needed to call for help. I could hear and think just fine, but I could not react. It was like I was a little bit asleep and could not control my body. When we heard the ambulance, my friend tucked me into my table so that I would not fall and went to open the door. The problem was he caught my accessed port between me and the table and it hurt, so I tried to push away and ended up falling out of the table and onto the floor which is where the paramedics found me.
They gave me some oxygen via a c-pap (I think) and an Albuteral breathing treatment. After those two things I was alert and actually felt for a bit that I need not even bother with the hospital (ha! that is SOO me!) Nevertheless, I was taken to the ER. When I got there, luckily, the BEST RT was called and being familiar with CF, she had everything in motion: I received another breathing treatment, she called my CF doc (who heads the ICU at the hospital), I had an arterial blood gas drawn and was told fairly quickly that my CO2 levels were quite high (62.5) and so I got to wear the bi-pap Darth Vader mask from hell. This ended up causing a lot of my problems. So anyway.
Now my mom and dad and husband and kids had made it to the hospital. My parents were very worried, and while I understand why, they caused me a great deal of anxiety with how they reacted to the situation and new boundries MUST be drawn before anything like this ever happens again. I am a bit irritated still about how the situation was handled in the beginning. I want to reiterate that I have a HUGE loving and supportive family, but it was spearheaded by two people who have had very little interaction with my disease over the years, and thus were a little bit misinformed, and were too blinded by their own worry to think rationally. I don't blame them for this, but I'm lying if I don't admit to some resentment about how they acted when I needed them to be calm and cool.
Ok. so I was admitted to the ICU on the bi-pap and I was miserable. My RT wanted my bi-pap settings very high in order to eliminate some of the CO2 in my system but this was extremely uncomfortable for me. If you don't breathe with the bi-pap it feels like you cannot breathe at all. Occasionally I felt that the machine was making me hyperventilate and then my family was trying to come in and talk to me - which at times was fine, but occasionally I got so irate with them that I would start to panic. I'm also clausterphobic and the bi-pap mask was giving me a great deal of anxiety.
My mom called my entire family. I mean ENTIRE. My brother flew in from California, that's what I mean. And my step-mom called the minister from her and my dad's church. Can you imagine seeing this from my point of view? What exactly were they doing? What were the thinking? DId they know something I did not know? I was angry that they were all coming to say goodbye. No matter what they say ("we were just there to support you" - um no. Because if you wanted to support me you would not have made me a circus freak that you all stared at from the hallway), they were there in case I died. That was fucked up and it makes me mad. These words might be enough to make my family very upset with me, but the fact of the matter is my doctor never said anything remotely like, "She has 24 hours to live." It was all reactionary. and it did not calm me in any way. So, sorry guys. I love you, but next time, please wait for the death proclamation before rushing to my bedside in droves. Yes, I am a bitch. Sorry. I don't think my family reads my blog, so maybe they will remain oblivious to this? If not, all I'm saying is PLEASE LISTEN TO HOW I FEEL. Thank you.
So at this point everything gets hazy. I know that my abdomen became painful and distended and some of that was the bi-pap forcing so much air into me. I was miserable. I know I was given a shot of morphine at some point in the night with the hopes it would make me sleep. and I know my nurse that first night and I did not get along very well. I give her credit that she probably did all for me that she was allowed to do, but she just could not do enough to fix my misery and I was super annoyed with her. She did express her irritation with me unkindly though and I won't forget that trauma.
My sense of time is skewed, but at some point Friday afternoon I requested to be vented. I could not take the pain and anxiety any longer and I wanted to be sedated and oblivious. I think that this request came at the relief of much of the staff as I had initially been very against a vent. You know your sick and exhausted when things like a ventilator start to sound good.
The last thing I really remember was my doc saying, "So you want to be intubated?" and nurses pulling supplies out all over the place.
I'm told that I was then heavily sedated and put on the vent at 100% vent dependent. I remember nothing from that point until maybe Monday or Tuesday when they began turning down the vent and the sedative. then I was able to read some FB, write notes to people about what I wanted/needed, etc. Still, the notes that I was writing at that time, some are pretty funny and I have no idea what I was talking about.
Actually, I do remember on Sunday that my Infectious Disease doc changed my antibiotic...so I guess maybe I was a little bit aware. Anyway, by this time only my mom, dad, step-mom, and close friends were coming up to see me as well as my husband and the kids so though I sometimes found these visits exhausting, I wasn't irritated as I had been that first 24 hours. I do think and will probably always maintain that having visitors in the hospital sucks and your forced to give attention and energy to people who often don't give you a choice if you want to see them, they just show up. My friend Laura texted before she came, which was nice, and my kids wanted to see their mom, so I couldn't be upset about that, though they did tire me a bit. Still, I am lucky and loved and I have not lost sight of that. It would have been far worse to have no one come rather than to have too many people. My internet family really sustained me. The beauty of the internet is that you can deal with people when you want to, but there is no shortage of love and support either. I am so grateful for everyone who cared for me and prayed or sent intentions or whatever people do during these times. This was far harder, and will continue to be so, on my family than it was on me. Hell, I spent a good portion of the thing in propofol land with Michael Jackson.
My family, not completely understanding transplant, got it into their heads that TX is the logical next step. I'm pretty sure I am still too healthy for TX and I am certainly sure that I am NOT certain about TX. I KNOW I am not ready for TX yet, even if I was deemed worthy. No way. But I have been listening to a lot of TX and religious propaganda from my fam and it's hard not to be annoyed. I saw something I wrote on FB when my mom put a call out for prayers that I wrote that it "is their belief in the occult that is helping" and I know at one point I got mad at my dad and drew a 6 pointed star, lol, so feistiness never quite left the building and I haven't changed my ideas about any of that, no matter how much whispering they did in my sedated ears.
So, that's pretty much it. On Wednesday of the next week they significantly turned the vent down and on Thursday it was at only 5% and after my 150,000th ABG draw the tube was pulled (disgusting and horrifying) and then it was just a matter of hanging out. I was sent up to a regular floor Friday morning and was discharged Monday afternoon, 12 days after I went in.
I have been doing much much better. Today I went a few hours without O2 with no desatting and I have my follow up appointment next Thursday, the same day I start work on a new tattoo, a mermaid with the word "adapt" worked into the piece as an homage to life with CF and being a mom and wife and all these different hats I wear every day. I make them each work in whatever way I can.
So...I have to go back to the end of March to really begin. Maybe all the way back to November. In November I had this crazy pain in my right lung. It was almost intolerable though I did tolerate it for about 10 days because I knew I had a clinic visit coming up and I try not to do ANYTHING remotely CF related outside of my clinic because, for you non-CFers out there - the medical profession at large really knows very very little about CF and you wind up in a big cluster fuck of nonsense of you try to get anything accomplished without your CF team on board.
Anyway, I had an x-ray which demonstrated a right middle lobe atelectasis (basically it's like a collapsed lobe) and I had my first bronchoscopy. I think this was in November...maybe it was in January? I was definitely in the hospital in November and January (and March and April/May), though my timing might be off here. Either way, I ended up admitted again in January for the SAME infection.
My normal routine is to go into the hospital where I am desensitized to the antibiotics I need because I am allergic to them and then I finish up the course of abx at home. During my Jan admission I desatted during my sleep and required supplemental oxygen - which isn't weird for a sick CFer, but I didn't know it was going to be a thing.
Then it was March and I was sick, again. Once again, I put things off until I had my clinic appointment. I had my usual pulmonary function test and my FEV1 was 35%!! My baseline is about 55% so that's a significant dip. My doc ordered a CT, another bronch, and an admission for more IVs. The thing was, I had plans to go to CA the beginning of April that I wasn't willing to put off. Quality over quantity I rationalized. I did have the CT before I left.
CA wasn't that fun, simply because I felt like SHIT. I was so damn tired the entire time. I was almost relieved to be going to the hospital and I actually stayed for 4 days instead of my usual 24 hours. It was at this time that my need for continuous O2 was discovered. My oxygen sats actually went down to 77% at one point before I was put on 3L of O2. I was not taken off the O2 upon being released from the hospital and was told the only way I was going home was to go home with oxygen.
Wearing O2 and carrying a tank with you everywhere you go SUCKS. And it's pretty hard to convince your family that your OK when you have an oxygen cannula stuck to your face. So once I was realeased, I found myself resisting going places more and more. Which was OK because I really wasn't feeling well still. at.all.
My doc put me on an IV med called Meropenem, an inhaled med called Cayston, and an oral antibiotic called Zyvox. Zyvox is a nasty drug. It gave me terrible lethargy and the worst diarrhea of my life. I chalked feeling so poorly up to that medicine. As well, I found that if I wore the O2 at home and in the car, I really didn't feel THAT BAD if I took it off to run into the grocery store or the kids' schools. haha. little did I know.
So on Thursday, April 25th (I think), Miss M had a "Muffins for Moms" event at her school. I was there for about an hour and I left the O2 in the car.
I am going to back up a tiny bit to complain for a minute. My family were kind of dicks to me during this time. I asked for help a few times and mentioned more than once that I just wasn't feeling well and I was told to "step it up" and "quit complaining" by two of my family members. In their defense, I have spent the last 35 years pretending everything is fine, even when it hasn't been, so they really didn't know. But I mention that because 1) it comes into play about how I feel regarding fam later and 2) I was pushing myself really hard to feel that I accomplished something during the daytime rather than having to face everyone and say NO, I didn't do the laundry, NO I didn't make dinner, NO I haven't swept the floors. Retrospectively, who gives a fuck, right? But I felt guilty about doing nothing all day.
So, anyway, after "Muffins for Moms" I went home, stuck on the O2 and proceeded to watch a bunch of "Arrested Development" episodes. About 1 that afternoon a friend stopped by. This friend was a boy but not a romantic boy. Still, when the doorbell rang my vanity kicked in, and I locked up the dog, hung the O2 cannula on the doorknob and answered the door.
My friend knew I was on O2 and even said that he could see the indentations from the cannula and asked why I took it off. I shrugged and said, "No big deal, you will only be here for a few minutes anyway." We both noted how out of breath I was. I could not seem to catch my breath and I lamented how weird that was, as I had been wearing the oxygen all day and had only gotten up to answer the door.
I decided I needed the O2 after all and went into the other room to get the cannula. By the time I sat back down my dexterity seemed to be impeded and I could not get the cannula over my ears. Then I noticed my friend seemed to be going in slow motion. I said something was wrong. Then I started to pass out. It was like I was the drunkest I have ever been. I could not keep my head up or eyes open and I was trying to hold the O2 to my nose because I still could not get it on. I told him he needed to call for help. I could hear and think just fine, but I could not react. It was like I was a little bit asleep and could not control my body. When we heard the ambulance, my friend tucked me into my table so that I would not fall and went to open the door. The problem was he caught my accessed port between me and the table and it hurt, so I tried to push away and ended up falling out of the table and onto the floor which is where the paramedics found me.
They gave me some oxygen via a c-pap (I think) and an Albuteral breathing treatment. After those two things I was alert and actually felt for a bit that I need not even bother with the hospital (ha! that is SOO me!) Nevertheless, I was taken to the ER. When I got there, luckily, the BEST RT was called and being familiar with CF, she had everything in motion: I received another breathing treatment, she called my CF doc (who heads the ICU at the hospital), I had an arterial blood gas drawn and was told fairly quickly that my CO2 levels were quite high (62.5) and so I got to wear the bi-pap Darth Vader mask from hell. This ended up causing a lot of my problems. So anyway.
Now my mom and dad and husband and kids had made it to the hospital. My parents were very worried, and while I understand why, they caused me a great deal of anxiety with how they reacted to the situation and new boundries MUST be drawn before anything like this ever happens again. I am a bit irritated still about how the situation was handled in the beginning. I want to reiterate that I have a HUGE loving and supportive family, but it was spearheaded by two people who have had very little interaction with my disease over the years, and thus were a little bit misinformed, and were too blinded by their own worry to think rationally. I don't blame them for this, but I'm lying if I don't admit to some resentment about how they acted when I needed them to be calm and cool.
Ok. so I was admitted to the ICU on the bi-pap and I was miserable. My RT wanted my bi-pap settings very high in order to eliminate some of the CO2 in my system but this was extremely uncomfortable for me. If you don't breathe with the bi-pap it feels like you cannot breathe at all. Occasionally I felt that the machine was making me hyperventilate and then my family was trying to come in and talk to me - which at times was fine, but occasionally I got so irate with them that I would start to panic. I'm also clausterphobic and the bi-pap mask was giving me a great deal of anxiety.
My mom called my entire family. I mean ENTIRE. My brother flew in from California, that's what I mean. And my step-mom called the minister from her and my dad's church. Can you imagine seeing this from my point of view? What exactly were they doing? What were the thinking? DId they know something I did not know? I was angry that they were all coming to say goodbye. No matter what they say ("we were just there to support you" - um no. Because if you wanted to support me you would not have made me a circus freak that you all stared at from the hallway), they were there in case I died. That was fucked up and it makes me mad. These words might be enough to make my family very upset with me, but the fact of the matter is my doctor never said anything remotely like, "She has 24 hours to live." It was all reactionary. and it did not calm me in any way. So, sorry guys. I love you, but next time, please wait for the death proclamation before rushing to my bedside in droves. Yes, I am a bitch. Sorry. I don't think my family reads my blog, so maybe they will remain oblivious to this? If not, all I'm saying is PLEASE LISTEN TO HOW I FEEL. Thank you.
So at this point everything gets hazy. I know that my abdomen became painful and distended and some of that was the bi-pap forcing so much air into me. I was miserable. I know I was given a shot of morphine at some point in the night with the hopes it would make me sleep. and I know my nurse that first night and I did not get along very well. I give her credit that she probably did all for me that she was allowed to do, but she just could not do enough to fix my misery and I was super annoyed with her. She did express her irritation with me unkindly though and I won't forget that trauma.
My sense of time is skewed, but at some point Friday afternoon I requested to be vented. I could not take the pain and anxiety any longer and I wanted to be sedated and oblivious. I think that this request came at the relief of much of the staff as I had initially been very against a vent. You know your sick and exhausted when things like a ventilator start to sound good.
The last thing I really remember was my doc saying, "So you want to be intubated?" and nurses pulling supplies out all over the place.
I'm told that I was then heavily sedated and put on the vent at 100% vent dependent. I remember nothing from that point until maybe Monday or Tuesday when they began turning down the vent and the sedative. then I was able to read some FB, write notes to people about what I wanted/needed, etc. Still, the notes that I was writing at that time, some are pretty funny and I have no idea what I was talking about.
Actually, I do remember on Sunday that my Infectious Disease doc changed my antibiotic...so I guess maybe I was a little bit aware. Anyway, by this time only my mom, dad, step-mom, and close friends were coming up to see me as well as my husband and the kids so though I sometimes found these visits exhausting, I wasn't irritated as I had been that first 24 hours. I do think and will probably always maintain that having visitors in the hospital sucks and your forced to give attention and energy to people who often don't give you a choice if you want to see them, they just show up. My friend Laura texted before she came, which was nice, and my kids wanted to see their mom, so I couldn't be upset about that, though they did tire me a bit. Still, I am lucky and loved and I have not lost sight of that. It would have been far worse to have no one come rather than to have too many people. My internet family really sustained me. The beauty of the internet is that you can deal with people when you want to, but there is no shortage of love and support either. I am so grateful for everyone who cared for me and prayed or sent intentions or whatever people do during these times. This was far harder, and will continue to be so, on my family than it was on me. Hell, I spent a good portion of the thing in propofol land with Michael Jackson.
My family, not completely understanding transplant, got it into their heads that TX is the logical next step. I'm pretty sure I am still too healthy for TX and I am certainly sure that I am NOT certain about TX. I KNOW I am not ready for TX yet, even if I was deemed worthy. No way. But I have been listening to a lot of TX and religious propaganda from my fam and it's hard not to be annoyed. I saw something I wrote on FB when my mom put a call out for prayers that I wrote that it "is their belief in the occult that is helping" and I know at one point I got mad at my dad and drew a 6 pointed star, lol, so feistiness never quite left the building and I haven't changed my ideas about any of that, no matter how much whispering they did in my sedated ears.
So, that's pretty much it. On Wednesday of the next week they significantly turned the vent down and on Thursday it was at only 5% and after my 150,000th ABG draw the tube was pulled (disgusting and horrifying) and then it was just a matter of hanging out. I was sent up to a regular floor Friday morning and was discharged Monday afternoon, 12 days after I went in.
I have been doing much much better. Today I went a few hours without O2 with no desatting and I have my follow up appointment next Thursday, the same day I start work on a new tattoo, a mermaid with the word "adapt" worked into the piece as an homage to life with CF and being a mom and wife and all these different hats I wear every day. I make them each work in whatever way I can.
Labels:
allergic reaction,
antibiotics,
anxiety,
cf clinic,
Cf fight,
children,
death,
hospital,
husband,
Oxygen,
parents,
ventilator
Friday, April 12, 2013
Just breathe
I haven't updated in a grip (haha). I'm posting from my phone because my computer is in the shop getting worked on, which makes posting tedious, but I've got plenty of free time and I'm overdue for a health post.
Things are fucked up. I'm
In the hospital for the 3rd time in 6 months and my situation is not getting better.
In fact, I'm on 3L of O2. I came in this morning for my second bronch in 4 months and at intake I was satting 85%! I told the nurse that had to be wrong and so she got another pulse ox which read the same, and so they then put me on 1.5L to start, but that wasnt enough so I was on 4L during and after bronch and we've found anything under 3L allows me to desat. As an example, I'm in the ICU for a desensitization and I took the cannula off to go to the restroom and fell into the 70s! Not good.
So it looks like I might be staying on oxygen for a while. I'm a bit freaked out, without a doubt. I've lost a significant amount of lug function in the last 6 mo and now don't seem to be exchanging blood gases very easily. :(
I'm definitely not stoked.
And, the icing on the cake is that I don't seem to be a photogenic oxygen wearer. I've come pretty hot cystics in O2. I tried, but I just don't think I'll make the cut. Sigh.
Woe is me.
Things are fucked up. I'm
In the hospital for the 3rd time in 6 months and my situation is not getting better.
In fact, I'm on 3L of O2. I came in this morning for my second bronch in 4 months and at intake I was satting 85%! I told the nurse that had to be wrong and so she got another pulse ox which read the same, and so they then put me on 1.5L to start, but that wasnt enough so I was on 4L during and after bronch and we've found anything under 3L allows me to desat. As an example, I'm in the ICU for a desensitization and I took the cannula off to go to the restroom and fell into the 70s! Not good.
So it looks like I might be staying on oxygen for a while. I'm a bit freaked out, without a doubt. I've lost a significant amount of lug function in the last 6 mo and now don't seem to be exchanging blood gases very easily. :(
I'm definitely not stoked.
And, the icing on the cake is that I don't seem to be a photogenic oxygen wearer. I've come pretty hot cystics in O2. I tried, but I just don't think I'll make the cut. Sigh.
Woe is me.
Saturday, February 2, 2013
"On Missing You"
I didn't write this, I copied and pasted from another person's entry on LiveJournal. I'm planning on writing again soon, and this gave me inspiration...it is so true to my here and now.
“On Missing You”
— Kristina H.
Here is the skin that you said you loved
draped over the back of the chair in the kitchen.
Here are the teeth. Here is the sternum, the
clavicle, the fibula. Here are the angel bones
laid out on top of the dresser like antique
jewelry. Here are the earlobes, the knobbly
elbows, the beauty mark near my temple
that always got a moan out of you. Here are
my thighs, my femur. All ten toes, all ten
fingers. My pubic bone, preserved and
wrapped in a velvet bag. Your name on the
tag. Your name on everything. Here is
the body that loved you. Here is the
heart, bloodied and wanting. Here are
those drunk voice mails, the sober texts.
Here is your promise of staying. Here
is the lonely hum in my brain where your
name used to be. Here is my spine. Here
is all the hollow. Here is all the longing. Here
is the heavy tongue, the scratchy vocal
chords. Here are all of the I love you’s.
Here is the shocking wreck of it all. Here is
how you were closer to me than my bones,
my skin. Here is the quiet city, your empty
side of the bed. Here is the empty. Here is not
knowing whether you loved me or not. Here is
the poem that can’t save us. Here.
“On Missing You”
— Kristina H.
Here is the skin that you said you loved
draped over the back of the chair in the kitchen.
Here are the teeth. Here is the sternum, the
clavicle, the fibula. Here are the angel bones
laid out on top of the dresser like antique
jewelry. Here are the earlobes, the knobbly
elbows, the beauty mark near my temple
that always got a moan out of you. Here are
my thighs, my femur. All ten toes, all ten
fingers. My pubic bone, preserved and
wrapped in a velvet bag. Your name on the
tag. Your name on everything. Here is
the body that loved you. Here is the
heart, bloodied and wanting. Here are
those drunk voice mails, the sober texts.
Here is your promise of staying. Here
is the lonely hum in my brain where your
name used to be. Here is my spine. Here
is all the hollow. Here is all the longing. Here
is the heavy tongue, the scratchy vocal
chords. Here are all of the I love you’s.
Here is the shocking wreck of it all. Here is
how you were closer to me than my bones,
my skin. Here is the quiet city, your empty
side of the bed. Here is the empty. Here is not
knowing whether you loved me or not. Here is
the poem that can’t save us. Here.
Tuesday, August 7, 2012
when I pass by all the people say: just another guy on the lost highway
Tonight is the 8th anniversary of my marriage, but I am alone. This is not news to some, maybe to others, and maybe it's irrelevant to many. but to me it seems significant.
Thinking back on our time together, eleven years, it seems that the turning point came early on: a Fourth of July, very soon after our first year together, after declarations of love - which I personally do not give easily, had been made.
I was moving into my first home, a newly independent mother and college graduate. I was a bilingual education teacher enamored with the new cultures where I found myself daily and with this new relationship, one that actually felt real and adult, capable of blossoming along with me.
Simultaneously, he was divorced, moving out of his childhood home which he had purchased and struggling to survive as a single man, a part-time dad. I can understand this now, but certainly not then, and while I'm sure his perspective is different, he had not tread these waters before either.
I often wonder if examining these early years will reveal the answers of what was to come, an overshadowing of my own history? Maybe this is simply hindsight, or, what I often succumb to when writing: literary appeal? But surely there were lines being drawn at this time: powershifts and independence, loneliness, selfishness and fear ribboning around each of us, pulling us tight where we could not breathe, where we'd trip and bleed because we tied the ribbons together too tightly. There was blame and anger and pulling and stretching those ribbons into the skin like wires until flow was cut off to other parts. Yet when one bled, the other held the cool cloth, despite our own ribboned appendages, ribcages, teeth, and hearts. It became a weary kind of dance we did, to untangle the ribbons, each independently without twists or chinks, retying some tighter, letting some flow loose, but never ever letting go of the end of our strand.
So we worked through that next year with ribbons and scissors, trying to cut out and create a fit for us and for a while the future looked good, that maybe we 'd tied our hearts together just right, pehaps even with ribbon to spare; just enough silken spiral with which to spin ourselves a little bit free, just enough to lash the ribbon too tightly together heart-to-heart, breast-to-mouth, just enough to hang ourselves.
We tied and untied those ribbons for years, not paying attention when the ends began to unravel, and maybe we even stopped caring about our own ends of ribbon,at least i did mine, breaking the ties in anger and frustration only to lash the ends back together over and over. Can you imagine the mess? Not to mention tied up in this was one, then two homes, two, then three children, dogs, cars, bills, and then maybe nothing but a goddamn mess of string.
This story is about me though. I'm writing my way out of that web, the only way I know how, with words.
I collect lonely people, and like spoons, knives, and forks, all clanking together in the same drawer, we all belong, without fitting together. I know lonely like the rise and fall of my labored breath, like I know exactly when the cough will end, when my lungs will finally give in and spit out their ransom. I know lonely people. Broken birds. They are all around me, strung along throughout my life in sentence. Each though, a small constellation bringning me some light in the dark. I like the dark, something many don't understand, but if you do, you do, and if you do, then I'll bet somewhere along the way, our stars have crossed.
When I think about it, some maybe were not as lonely as I thought or as they presented themselves to be. I've been called mysterious more than once, but it's a falsehood. It's simply shy and alone. Alone isn't bad though, and that is the fact I have the most problem bringing to paper. The romance of lonely is hard to relsease to words. I know more than one pseudo-lonely soul made their way past my door for a night or two before I wisened up to their lack of real lonesome appeal. Too much bravado, too many words spoken and not enough whispers, a lack of something tangible in the dark. And the older I got, after I was married, when random nights spent unalone became a thousand and one nights alone with other people, I started to crane my ear to the chime of the computer, where the other lonelies, the truly alone, sat in some other place in some other world, our interactions a silent radioactive arc in which the only ways we lay entwined were with the words we spun.
I've now lost many of these friends. I know it is a direct result of the people I choose to interact with, though by no fault of anything other than faulty genes. I might be losing my husband in an entire different manner. I worry I am losing my almost-teenaged son. These losses have created a lethargy in me that somedays feels to heavy to overcome, and while I often felt a self pity that my suffering has gone unnoticed, I know that I turned away from any peering eyes into my despair. Because that is what lonely people do. We are alone. It's not a fault or a chemical problem, it just is. and along the way, I lost first one friend, then another, then my world, strung together by wirds was turned upside down by words untrue and I felt like concrete was being poured on my already drowning body and I could not, did not, care to breathe.
Caring for another lonely person, a bird I cannot fix, gives me purpose. It's a secret I've long kept concealed and which I know now to be futile, but I don't care. I cannot fix anyone, but the intent to try, a co-dependent tsumani, gives me some reason to listen, again. And here I leave a millions words unwritten, unsure who might read and what might be inferred, when I know all I have done is put thought to "paper." How easy it might be to slide down and allow my own words to become untrue, tied together only to buoy my lonely heart?
Thinking back on our time together, eleven years, it seems that the turning point came early on: a Fourth of July, very soon after our first year together, after declarations of love - which I personally do not give easily, had been made.
I was moving into my first home, a newly independent mother and college graduate. I was a bilingual education teacher enamored with the new cultures where I found myself daily and with this new relationship, one that actually felt real and adult, capable of blossoming along with me.
Simultaneously, he was divorced, moving out of his childhood home which he had purchased and struggling to survive as a single man, a part-time dad. I can understand this now, but certainly not then, and while I'm sure his perspective is different, he had not tread these waters before either.
I often wonder if examining these early years will reveal the answers of what was to come, an overshadowing of my own history? Maybe this is simply hindsight, or, what I often succumb to when writing: literary appeal? But surely there were lines being drawn at this time: powershifts and independence, loneliness, selfishness and fear ribboning around each of us, pulling us tight where we could not breathe, where we'd trip and bleed because we tied the ribbons together too tightly. There was blame and anger and pulling and stretching those ribbons into the skin like wires until flow was cut off to other parts. Yet when one bled, the other held the cool cloth, despite our own ribboned appendages, ribcages, teeth, and hearts. It became a weary kind of dance we did, to untangle the ribbons, each independently without twists or chinks, retying some tighter, letting some flow loose, but never ever letting go of the end of our strand.
So we worked through that next year with ribbons and scissors, trying to cut out and create a fit for us and for a while the future looked good, that maybe we 'd tied our hearts together just right, pehaps even with ribbon to spare; just enough silken spiral with which to spin ourselves a little bit free, just enough to lash the ribbon too tightly together heart-to-heart, breast-to-mouth, just enough to hang ourselves.
We tied and untied those ribbons for years, not paying attention when the ends began to unravel, and maybe we even stopped caring about our own ends of ribbon,at least i did mine, breaking the ties in anger and frustration only to lash the ends back together over and over. Can you imagine the mess? Not to mention tied up in this was one, then two homes, two, then three children, dogs, cars, bills, and then maybe nothing but a goddamn mess of string.
This story is about me though. I'm writing my way out of that web, the only way I know how, with words.
I collect lonely people, and like spoons, knives, and forks, all clanking together in the same drawer, we all belong, without fitting together. I know lonely like the rise and fall of my labored breath, like I know exactly when the cough will end, when my lungs will finally give in and spit out their ransom. I know lonely people. Broken birds. They are all around me, strung along throughout my life in sentence. Each though, a small constellation bringning me some light in the dark. I like the dark, something many don't understand, but if you do, you do, and if you do, then I'll bet somewhere along the way, our stars have crossed.
When I think about it, some maybe were not as lonely as I thought or as they presented themselves to be. I've been called mysterious more than once, but it's a falsehood. It's simply shy and alone. Alone isn't bad though, and that is the fact I have the most problem bringing to paper. The romance of lonely is hard to relsease to words. I know more than one pseudo-lonely soul made their way past my door for a night or two before I wisened up to their lack of real lonesome appeal. Too much bravado, too many words spoken and not enough whispers, a lack of something tangible in the dark. And the older I got, after I was married, when random nights spent unalone became a thousand and one nights alone with other people, I started to crane my ear to the chime of the computer, where the other lonelies, the truly alone, sat in some other place in some other world, our interactions a silent radioactive arc in which the only ways we lay entwined were with the words we spun.
I've now lost many of these friends. I know it is a direct result of the people I choose to interact with, though by no fault of anything other than faulty genes. I might be losing my husband in an entire different manner. I worry I am losing my almost-teenaged son. These losses have created a lethargy in me that somedays feels to heavy to overcome, and while I often felt a self pity that my suffering has gone unnoticed, I know that I turned away from any peering eyes into my despair. Because that is what lonely people do. We are alone. It's not a fault or a chemical problem, it just is. and along the way, I lost first one friend, then another, then my world, strung together by wirds was turned upside down by words untrue and I felt like concrete was being poured on my already drowning body and I could not, did not, care to breathe.
Caring for another lonely person, a bird I cannot fix, gives me purpose. It's a secret I've long kept concealed and which I know now to be futile, but I don't care. I cannot fix anyone, but the intent to try, a co-dependent tsumani, gives me some reason to listen, again. And here I leave a millions words unwritten, unsure who might read and what might be inferred, when I know all I have done is put thought to "paper." How easy it might be to slide down and allow my own words to become untrue, tied together only to buoy my lonely heart?
Labels:
death,
depressing,
husband,
lonely bug,
understadning
Thursday, May 10, 2012
Been a long time been a long lonely lonely time
Has it really been since October since I've written? Good grief! I have to get back into the swing of things.
My mind is turning over several ideas right now, but I think I'll just write and see what transpires."65_Redroses" made its US debut on OWN last week.
I hadn't planned on watching. A friend was able to get me a VHS tpe from the Canadian CBC broadcast and I had already watched that twice. I've cried everytime I have watched the film. (POSSIBLE SPOILER BELOW). I cry for Eva, mostly, but myself also. I know how the story ends. It was about the time that begins filming that I became friends with Meg and Eva. Meg reminded me (and still does!) of myself in so many ways and Eva accepted her situation with such grace and beauty and such a great outlook. One thing that I learned from Eva was to try to let myself be loved. I'm great at giving love, not so good at accepting it. CF taught me to turn people away. I have never wanted special consideration or treatment. I want to be left alone. this is very hard for a lot of people to understand - and I still mean it yet. I truly enjoy being alone. My username online for almost as long as the internet has existed has been wanderlost, taken from the Tolkein quote, "All who wander are not lost." I saw this on a bumper sticker when I was about 18 years old and it really resonated with me. It's exactly how I feel - just because I have my own path, my own direction, it doesn't mean that I need help. I am not lost (some may beg to differ, lol).I still want to be alone. I do not mind solitude. For this reason the internet has always been enticing. I can have commraderie and friendship at my own pace. if I don't want to talk, I don't open my chat box. If I want to chat in my panties while eating potato chips and drinking wine, I can. The rules of the internet are differnet. I am me in words. and me in words has always been the better me. I think that many of us here in webland feel the same way. The computer is a safety zone from mundane, awkward human interaction. I detest small talk. Truly, I hate it. I shy away from it. for this reason I sometimes don't even answer my telephone, because to get to anything real, one usually must engage in the motions of small talk. The internet, to some extent, diminishes this need. even in chat rooms and private messenging, there is small talk, but to me, it's just so much easier to write it out and get it over with.
**I started writing this entry in may abd never finished,so I'm just going to publish it now to get this blog up DVD humming again. I am a writer, therefore, I need to quit bullshitting and start writing!!
My mind is turning over several ideas right now, but I think I'll just write and see what transpires."65_Redroses" made its US debut on OWN last week.
I hadn't planned on watching. A friend was able to get me a VHS tpe from the Canadian CBC broadcast and I had already watched that twice. I've cried everytime I have watched the film. (POSSIBLE SPOILER BELOW). I cry for Eva, mostly, but myself also. I know how the story ends. It was about the time that begins filming that I became friends with Meg and Eva. Meg reminded me (and still does!) of myself in so many ways and Eva accepted her situation with such grace and beauty and such a great outlook. One thing that I learned from Eva was to try to let myself be loved. I'm great at giving love, not so good at accepting it. CF taught me to turn people away. I have never wanted special consideration or treatment. I want to be left alone. this is very hard for a lot of people to understand - and I still mean it yet. I truly enjoy being alone. My username online for almost as long as the internet has existed has been wanderlost, taken from the Tolkein quote, "All who wander are not lost." I saw this on a bumper sticker when I was about 18 years old and it really resonated with me. It's exactly how I feel - just because I have my own path, my own direction, it doesn't mean that I need help. I am not lost (some may beg to differ, lol).I still want to be alone. I do not mind solitude. For this reason the internet has always been enticing. I can have commraderie and friendship at my own pace. if I don't want to talk, I don't open my chat box. If I want to chat in my panties while eating potato chips and drinking wine, I can. The rules of the internet are differnet. I am me in words. and me in words has always been the better me. I think that many of us here in webland feel the same way. The computer is a safety zone from mundane, awkward human interaction. I detest small talk. Truly, I hate it. I shy away from it. for this reason I sometimes don't even answer my telephone, because to get to anything real, one usually must engage in the motions of small talk. The internet, to some extent, diminishes this need. even in chat rooms and private messenging, there is small talk, but to me, it's just so much easier to write it out and get it over with.
**I started writing this entry in may abd never finished,so I'm just going to publish it now to get this blog up DVD humming again. I am a writer, therefore, I need to quit bullshitting and start writing!!
Saturday, October 15, 2011
being lonely is a habit, like smoking or taking drugs - I quit them both, but man was it rough
I haven't been myself for sometime now. Probably a few years, but particularly the past 2 years and most acutely the past 10 months. I know the reasons for a lot of this. It's just that I kept believing that I was in a funk and that I'd snap out of it. I mean, we all go down in the hole from time to time, don't we? The thing is, I haven't been able to crawl out. I am in deep. I finally decided it was time to give myself a diagnosis. Situational depression is certainly part of it, but the past 10 months can only be filed away in one place that I can see: Post traumatic stress disorder. I have nearly every symptom listed and it's all following a catastropichally horrid even that took place January 13th and has unfoled over the past 10 months.
Symptoms of PTSD fall into three main categories:
1. "Reliving" the event, which disturbs day-to-day activity
•Flashback episodes, where the event seems to be happening again and again
•Repeated upsetting memories of the event
•Repeated nightmares of the event
•Strong, uncomfortable reactions to situations that remind you of the event
2. Avoidance
•Emotional "numbing," or feeling as though you don't care about anything
•Feeling detached
•Being unable to remember important aspects of the trauma
•Having a lack of interest in normal activities
•Showing less of your moods
•Avoiding places, people, or thoughts that remind you of the event
•Feeling like you have no future
3. Arousal
•Difficulty concentrating
•Startling easily
•Having an exaggerated response to things that startle you
•Feeling more aware (hypervigilance)
•Feeling irritable or having outbursts of anger
•Having trouble falling or staying asleep
Just writing about this makes me want to cry. I've been hiding out in my house in the shroud of my fear as if my fear and vigilance will protect me.
I've realized that I have not got much faith. I mean, yes, I have always been a person who has prayed for guidance and help, for protection of myself or my children, to express gratitude. But I've never had faith that 'god knows' what's best, or that things happen for a reason or that if I just put my faith and trust into a power greater than myself that things will happen as they should. I'm terrified to relase that kind of control, even if that control is an illusion.
It's an angry circle that I can't get out of. I haven't even been doing treatments, if I'm to be really honest. I just don't care. I don't have the motivation to do anything than the basic requirements. I am miserable, but I don't know how to get out of it. I will make plans: get on the treadmill, sew something, do just one treatment for the day - but when the time comes, I just can't. I take my kids to school; I do the housework required of me; I teach my class and grade the students' papers. I do what I have to do, but that's where it all ends.
Quit moping. Get it together. You're crazy. It will be good for you. Just do it. you're selfish. Let it go. Stop living in fear. It's your own fault. If only you'd...
all these words swirl around me, in my own head and spit out by others. Some mean well, some are angry with me. Everyone is probably frustrated.
I am not trying to be like this. Honest to god. If I could afford a psychiatrist I'd go. Though meds, meds, meds. The answer to everything, right?
I just can't help it. Certain painfu episodes play over and over in my head. I imagine people gloating at my pain. I want to hurt somewhere besides my heart. I want to stop hurting. I think I've cried everyday for 10 months. That's like 300 days of tears. I hold my fear so tightly. I was doing OK, maybe up until we returned from Costa Rica and then things - precariously built up - toppled over and I've been stuck under the rubble since.
I don't want help. I do. I don't want someone to pull me from my bed and slap some sense into me, but maybe I need it. I have never been like this before and I keep waiting for it to end. But some of my thoughts don't have an ending that ends well.
If I didn't have my kids - as much as I feel like a crap mom - I don't know where I'd be. Maybe somewhere tropical, maybe dead. They are a buoy. They keep me here, grounded, but also they keep me here. Running away isn't as easy with two lives under your care.
I don't want responses. I don't want to hear anyone cares, I want to be me again. I want the hurting to stop. I want to stop being afraid. I wish for a faith strong enough to carry me through
"Jesus and Mary, can you carry us through this ocean into the arms of forgiveness."
Symptoms of PTSD fall into three main categories:
1. "Reliving" the event, which disturbs day-to-day activity
•Flashback episodes, where the event seems to be happening again and again
•Repeated upsetting memories of the event
•Repeated nightmares of the event
•Strong, uncomfortable reactions to situations that remind you of the event
2. Avoidance
•Emotional "numbing," or feeling as though you don't care about anything
•Feeling detached
•Being unable to remember important aspects of the trauma
•Having a lack of interest in normal activities
•Showing less of your moods
•Avoiding places, people, or thoughts that remind you of the event
•Feeling like you have no future
3. Arousal
•Difficulty concentrating
•Startling easily
•Having an exaggerated response to things that startle you
•Feeling more aware (hypervigilance)
•Feeling irritable or having outbursts of anger
•Having trouble falling or staying asleep
Just writing about this makes me want to cry. I've been hiding out in my house in the shroud of my fear as if my fear and vigilance will protect me.
I've realized that I have not got much faith. I mean, yes, I have always been a person who has prayed for guidance and help, for protection of myself or my children, to express gratitude. But I've never had faith that 'god knows' what's best, or that things happen for a reason or that if I just put my faith and trust into a power greater than myself that things will happen as they should. I'm terrified to relase that kind of control, even if that control is an illusion.
It's an angry circle that I can't get out of. I haven't even been doing treatments, if I'm to be really honest. I just don't care. I don't have the motivation to do anything than the basic requirements. I am miserable, but I don't know how to get out of it. I will make plans: get on the treadmill, sew something, do just one treatment for the day - but when the time comes, I just can't. I take my kids to school; I do the housework required of me; I teach my class and grade the students' papers. I do what I have to do, but that's where it all ends.
Quit moping. Get it together. You're crazy. It will be good for you. Just do it. you're selfish. Let it go. Stop living in fear. It's your own fault. If only you'd...
all these words swirl around me, in my own head and spit out by others. Some mean well, some are angry with me. Everyone is probably frustrated.
I am not trying to be like this. Honest to god. If I could afford a psychiatrist I'd go. Though meds, meds, meds. The answer to everything, right?
I just can't help it. Certain painfu episodes play over and over in my head. I imagine people gloating at my pain. I want to hurt somewhere besides my heart. I want to stop hurting. I think I've cried everyday for 10 months. That's like 300 days of tears. I hold my fear so tightly. I was doing OK, maybe up until we returned from Costa Rica and then things - precariously built up - toppled over and I've been stuck under the rubble since.
I don't want help. I do. I don't want someone to pull me from my bed and slap some sense into me, but maybe I need it. I have never been like this before and I keep waiting for it to end. But some of my thoughts don't have an ending that ends well.
If I didn't have my kids - as much as I feel like a crap mom - I don't know where I'd be. Maybe somewhere tropical, maybe dead. They are a buoy. They keep me here, grounded, but also they keep me here. Running away isn't as easy with two lives under your care.
I don't want responses. I don't want to hear anyone cares, I want to be me again. I want the hurting to stop. I want to stop being afraid. I wish for a faith strong enough to carry me through
"Jesus and Mary, can you carry us through this ocean into the arms of forgiveness."
Labels:
depressing,
husband,
lonely bug,
sadness,
treatments
Friday, August 19, 2011
Singing you Away
So, at long last I have finished my master's thesis. It was entitled "Singing You Away:An Examination of Community and Self Discovery through Illness Narrative," and, for the most part, it was about all of YOU. Well, "YOU" being the generalized CF community that actually reads this blog. In honor of YOU, I decided to share a few blurbs here with YOU. The piece is going to be published by the University library as I think is the case with most Master's Theses (thesises)(?) (sp) and I am going to try to work it into a book length piece for publication. (so in other words, this shit is copyrighted, yo).
All I can say is thanks, because without YOU this piece would have never come to be. Chances are I'd still be writing about Edith Wharton. Not that that's not OK too, but this was more fun.
This is from the "context essay" - the academic part of my project:
"For most of my life I’ve had trouble revealing to people that I have the disease Cystic Fibrosis (CF). To any more than family, close friends, or medical staff, I’ve allowed the disease to remain tucked away inside of me, a secret I’ve been ashamed and embarrassed to admit. Even to those who knew about the disease, it was often unspoken; I only revealed my medical history if it was pertinent to the situation at hand. I denied that part of myself and hid it from others as well. Despite harboring the secret of my disease, I still often felt I had a story to tell. The hiding of the secret was, in fact, the story. I wanted to write a personal narrative which explained how, with the help of friends I made in the online Cystic Fibrosis community, I was able to release much of the embarrassment I felt surrounding my disease and accept that the illness was not a shameful secret, but rather just another part of who I am, no different from the color of my eyes or status of my belly button. The purpose of this essay is to find a place for my personal narrative, “Singing You Away,” within the academic conversation on illness narratives. I used two key terms from Arthur Frank’s work: the “cumulative epiphany” (Rhetoric 46), which is a narrative form in which the author comes to understand that the illness has always been a part of who he or she is, and the “dyadic body” (Wounded 35), a word Frank uses to refer to the shared experience of being bodies, in this case bodies who are afflicted with some kind of illness. I will examine these concepts later and refer to them throughout this essay as a means to examine the development and analysis of my personal narrative from a more theoretical perspective. Using these two concepts, I demonstrate how my narrative describes the development of my identity as a person with a disease and how, once I was able to accept that part of myself (particularly with the help of my online friends), I was able to use the medium of narrative to reveal my secret and assimilate the disease into my identity."
"I set the narrative up in short vignettes that pick out specific moments in my life that I felt could best shape the story. My aim was to show how I was born with this disease, rebelled against the life and medical prognosis that comes with a disease such as Cystic Fibrosis, and finally found some kind of peace with myself and the disease through the interactions I had online with other people who also had CF. These online interactions later play a large role in the way I hope to enter my voice into the genre of illness narrative, showing through my personal narrative the way that the internet changes the overall concept of illness writing. Narratives are now being written in real time, updated and changing daily through blogs and social networks as people update continually and interact with others as the disease is happening to them. Through these networks and friendships my personal narrative was shaped. These relationships helped to form my identity as a self with disease because as I read the continuing and ongoing stories of others with my same disease I could relate to them in a way that was not available to me at any other time in my life, either because I rejected it, or because the cross contamination risks of the disease were too great to take the chance of meeting in any other way than in a virtual reality. The relationships served as a mirror of sorts whereby I could compare my disease and myself to others with the same disease and examine how others dealt with their illness and disability, constantly comparing and contrasting that to my own reactions and experiences"
"The idea that life was to be shortened by CF has been a lingering stigma for my entire existence and was a motivating force in my narrative. I wanted to give voice to the deviation my story took as I struggled against this prognostication. I rebelled against the prognosis of CF long before CF made much of an appearance in my life’s narrative. I was rebelling against this “failed prognostication” that had shadowed me for years. In this memoir I’ve presented drug abuse as the primary mode that gave shape to that rebellion. Certainly substance abuse was not the only way I rebelled against my disease, but it is a serious way, and it is an intriguing way given the dire importance good health has in our society, especially when one has a life-shortening disease. Substance abuse is certainly not an issue of childhood and the fact that I was able to get to a point in life with this disease to be able to abuse narcotics is a rebellion of sorts against the disease and the prognostication of where that disease would take me. I should never have been healthy enough to even think about such a lifestyle. I did, however, and then even lived long enough to be able to look back on that time of life and put it to paper. This narrative itself is still a form of rebellion against the prognostication of medicine and society on the illness itself."
This next part is from the personal narrativepart of the project,or the "creative aspect." This is revealing more about me than I probably have to some of you - to others, you know all about this stuff cause you lived this life too. I hope the reader won't judge me too harshly based on how I acted 16 years ago. I am editing slighty, you know, just in case.
1995
She takes a swing and she can’t hit, she don’t mean no harm, she just don’t know what else to do about it
By my senior year of high school I had a handful of friends who had their own places. Bald Jay’s was next to a roachy pizza place on a street infested with hookers, winos, and other denizens of the smarmy South Bend street life. I’m amazed with our bravado in those days. Walking down streets not meant for suburban white girls, preening for the men who cat called, asking for drugs, going into the homes and cars of strangers to get them. I can’t believe we were never hurt; I think of how many ways we were hurt: taken advantage of, exploited, used.
I met Seth eight months after I’d decided to become a born-again virgin. I’d begun to grow weary of the meaninglessness in my interactions with boys. I was seventeen, heading soon for college. I wanted a fresh start; I wanted love. I had succeeded in creating a persona of wild,bad girl, but I started to envy my friends who had boyfriends who bought them flowers and took them on dates. I had visions of a relationship like the romance between Lloyd Dobler and Diane in "Say Anything," of Romeo and Juliet.
That last summer before college, my girlfriends and I had plans to follow the Grateful Dead. We wore second-hand clothes and ate lots of acid. My hair fell to my waist. I carried a one-hitter and a camera in a straw tote bag. I stopped shaving my legs. We were eighteen and free. It was the summer of my first true love.
I remembered Seth from high school. He had twirly eyes, like a cartoon character. I would see those kind of eyes only one time more in my life, in the eyes of a meth head in New Mexico, ironically also named Seth, who wanted a ride. The eyes would scare me. Seth’s eyes scared me. I’d heard the rumors: they all said he was wild. I’d never really paid him much attention until one summer evening at Bald Jay’s.
Like most teenagers’ first apartments, Bald Jay’s was sparsely furnished, the sink always full of dirty dishes. Band posters were tacked about the walls and the company was transient. People who weren’t even really friends with Jay would come by, his house one of the few to hang out in where there were no parents present. Erica and Lola, my closest friends, and I were frequent visitors, being friends with both Bald Jay and one of his roommates. We’d flounce into Jay’s unannounced in our gauzy skirts and sprawl across his couch assuming that our presence was always a welcome addition.
One night Seth slinked into the house and fell into a threadbare chair across from me. His energy was like honey, syrupy sweet. His hair was a tangle of auburn curls. He was shirtless, his chest flat and hard, bare. His army pants were pulled so low that the V of his pelvis was exposed, soft auburn curls peeking from the waistband. He rolled a joint, meticulously folding in the corners of the onion skin paper to make little pockets, then tapping out a sprinkling of cocaine from a magazine folded bindle he kept in the cellophane of his cigarette packet. I wasn’t even sure if he was aware that I was there. We all smoked: Seth and his friend Jake, Bald Jay, Lola, Erica, and I. We passed the joint from fingertip to fingertip, the raucous vibrations of Phish’s “Run like an Antelope” wafting from an upstairs bedroom, the windows open to the humid summer air and the rattling mufflers and loud voices of the downtown street life.
Soon after, Lola, Erica, and I went for a walk on the East Race, a pleasant boardwalk area built around the St. Joseph river. Our gypsy chains jingled, our patchouli drenched skin was soft in the lamplight as we discussed Seth and the cocaine laced joint and whether or not we thought we felt any different from it.
I decided to call Seth “Jim Morrison” in code because of a picture I’d had of the singer on my bedroom wall with the same wild wavy hair and low riding pants. I recruited Erica to help me track him down the next day. We found him on Van Buren Street, in the heart of run down South Bend, lying on a mattress in our friend Ray’s bedroom, smoking a joint. The four of us drove to Rum Village, a park and nature preserve on the southwest side of town, where we swung on the swings and smoked a joint in the woods. Seth massaged my shoulders from the backseat of my car as I drove us back to Ray’s and asked me to come over and go in his hot tub that night. I agreed and snuck out of my house via the sliding glass deck door to meet him at the end of my driveway. He picked me up in his white Honda Civic, a cigarette in hand, Jane’s Addiction on the tape player. My legs glimmered, slathered in the smoothness of Bath and Body works liquid talc....
It was an intense summer. We watched Perry Ferrell shoot up and pretend to be Dr. Rockstar in The Gift. Seth wore my dresses and let me put make-up on him. We had sex in the car, behind a church, in my mother’s house and his father’s, in the woods, in bathrooms. We took Xanax and drank microbrewed beer. We played pool and went to the beach. I was in love. Then he kissed a girl named Vanessa in his hot tub. And the boy I should have let go, of moral failing and intense addiction, I began to cling to even harder. I sobbed the night before I left for college and ate three of my mother’s Xanax bars. My heart was breaking.
When I got to college, still dating Seth long distance, I stopped smoking pot and started taking aerobics. I had the realization that no one was going to look after my health except me. I still drank, took hallucinogens, and did cocaine when we could find it, but I had this grand idea about saving my lungs. I didn’t tell anyone why, I just told them I was “allergic” to marijuana. This was an acceptable answer.
I hung out with hippies, bike thieves, druggies. Of all the people I was friends with in college, only a handful ever finished. Of those who did find success, many took the same roundabout path that I found myself on. The lure of Phish music and freedom was so enticing that working the midnight shift at the BP didn’t seem like a bad gig if it meant you could get all fucked up after and have no responsibility in between. I envied those people. Though I dallied in these fringe groups, I still felt a great deal of pressure to succeed both from my family and intrinsically. I was not going to fail at anything. So I compartmentalized. I could be smart; I could make Dean’s list and still stay up all night on cocaine. I further compartmentalized my CF. I’d left behind most of the people who’d known about it from my childhood, and told fewer and fewer people. I didn’t even tell my college roommate, Maria. Despite being friends in high school, it was several months into living together that one day she noticed me taking medicine before eating and asked me about it. I had no choice except between lying and telling the truth. I opted for the truth. I was embarrassed and played it off as nothing to worry about. I don’t remember telling her about the life expectancy, though I know I often threw that number in, especially as I got older and surpassed it, as a means to prove how unaffected I really was by the disease. A few years later I recall asking Maria about that day and what it was like to live with me during those years.
“Yeah, I do remember when you first told me that you had CF. It was at the very beginning of living in the dorms at BSU. Ryne and I were both there. I think the reason it came up was not about coughing, but as a way to explain why you were taking pills before eating. It was the first time I had ever even heard of CF,” she recalled as we mulled over a bottle of wine.
“I’m sure you told us all about it medically and stuff, but the part I remember most was you saying that most people don't live past 16, which sort of freaked me out. I had never really dealt with the mortality of a close friend. Eighteen is quite an invincible time for most.
“I remember after knowing, feeling protective of you when you would cough... I remember feeling pissed at people who would be like ‘Whoa dude, are you okay!?’ Or, ‘Damn girl, have another cigarette!’ Shit like that, but I would use my lack of concern to try and show them that they were dumb for asking: they should do the same. Looking back, I guess they weren't assholes, just concerned, but I felt sensitive to what I viewed as tactlessness and sort of a MYOB situation.”
Despite not smoking and exercising, two purposeful choices aimed at taking better care of my lung health, I still lived hard. College is a rough time for many coeds; binge drinking and crappy eating are commonplace, and I was no different. I was also warped into an increasingly codependent first love, something akin to a toddler in a Christmas tree shop: excitement, bright lights, and inevitable shattered glass.
Spring semester, Seth followed me to BSU and lived in the same residence hall on the floor below me. We spent most our nights in one another’s rooms. He peed in an empty two liter the nights he spent with me; I lined his trashcan with a plastic bag the nights I spent with him. Though I was modest around his roommate, Maria, Seth, and I were all comfortable with one another and often the three of us slept nude, Maria in her bed, Seth and I crammed into mine talking late into the night. There was something uninhibited about being so uninhibited and I found us all quite bohemian.
I wrote Seth’s papers for him, he rode me to class on the front of his bicycle. For spring break we headed to the Gila Mountains of New Mexico and the peaks of Breckenridge, Colorado with a slight detour to Palomas, Mexico to purchase and smuggle in valium. We both fell in love with the Southwest and vowed to return.
Jealousy had slyly sunk its fangs in our young love over the course of our time together. Less than a year into the relationship we’d both cheated on one another; it’s hard even now to understand why we continued to hang onto each other so fiercely. There was a sexual possession between us that I had never felt before and I wanted no other woman to have my man. It didn’t occur to me then that I wasn’t holding Seth responsible for his transgressions....
Seth transferred to the University of New Mexico the next semester. He and I visited one another each month after he left, once each driving ten hours to meet in Oklahoma for the weekend. I began the paperwork to take out loans to transfer to the University of New Mexico that spring. My parents were vehemently against the idea, Seth becoming nothing more to them than an impediment to my future successes. They truly feared that I would elope or become pregnant by him and bind myself to him even more fully than I already had.
My father, Seth, and I packed up my Toyota Corolla in January of 1997 and drove through the worst snowstorm the southwest had seen in years from Indiana to Albuquerque. My father had succumbed to the fact that he was helpless against me leaving, but he’d at least get me there safely.
The temperature was in the negatives as we drove through the Midwest. Not far out of Indiana we suffered a tear in the sidewall of the tire. Seth and I stood helplessly aside as my father unpacked the entire trunk of the car and attached the spare with his bare and frozen hands. The blowing snow and slippery conditions of the roads as we headed farther south convinced my father that only he should drive and we listened to him lament, “This isn’t good, this isn’t any fucking good” as he inched the car along the Texas highway.
New Mexico quickly became an exercise in addiction. My grades dropped to B’s. Retrospectively, this should have been a warning sign to my parents that something had gone amiss, but a B was still an acceptable grade and no one worried much. The truth was Seth and I spent some days awake on cocaine and some days in a groggy stupor of heroin. My resolve to help him with his addictions dissolved hours after I put my father on a plane back to Indiana.
We made friends with another couple and they were among the first new people I told that I had CF in years. I had no other answer but the truth for why I coughed so incessantly sometimes. Cocaine constricts the nasal passages and some nights the post-nasal drip would cause me to cough and gag without end. As with Maria, Seth was protective of me when someone joked about my coughing. He may have been the one who told them, in all actuality, as a response to some joke such as, “Maybe you need to see a doctor for that cough?”
“What does it taste like?” asked one of the friends. “Is it like when you have a cold?” I had no answer, my sputum always tasted the same; in effect, I always had a cold. I realized that their curiosity wasn’t a bad thing, it wasn’t a force of pity but rather a simple desire to understand. Talking was much easier with the fuel of drug-induced stimulation.
I knew that New Mexico wasn’t a healthy place for me to be. I never saw a doctor when I was there, I did not exercise, I was not eating well. I was clearly abusing drugs. The little cricket voice of my subconscious also knew that starting out my life with thousands of dollars of student loans wasn’t as good an idea as going home and letting my parents pay for my education. Seth scared me as his addiction spiraled farther and farther out of control and I was grasping at twigs trying not to follow him down. It was still important that I remain above water with my school work. The final straw was twofold: a worried phone call from my grandparents one week after we’d unplugged the phone and stayed in bed on a heroin binge, and a family trip to France that was held above me like a carrot on a stick: come home and you can go with us. My choice was made. After one semester and thousands of dollars, I was going back home."
All I can say is thanks, because without YOU this piece would have never come to be. Chances are I'd still be writing about Edith Wharton. Not that that's not OK too, but this was more fun.
This is from the "context essay" - the academic part of my project:
"For most of my life I’ve had trouble revealing to people that I have the disease Cystic Fibrosis (CF). To any more than family, close friends, or medical staff, I’ve allowed the disease to remain tucked away inside of me, a secret I’ve been ashamed and embarrassed to admit. Even to those who knew about the disease, it was often unspoken; I only revealed my medical history if it was pertinent to the situation at hand. I denied that part of myself and hid it from others as well. Despite harboring the secret of my disease, I still often felt I had a story to tell. The hiding of the secret was, in fact, the story. I wanted to write a personal narrative which explained how, with the help of friends I made in the online Cystic Fibrosis community, I was able to release much of the embarrassment I felt surrounding my disease and accept that the illness was not a shameful secret, but rather just another part of who I am, no different from the color of my eyes or status of my belly button. The purpose of this essay is to find a place for my personal narrative, “Singing You Away,” within the academic conversation on illness narratives. I used two key terms from Arthur Frank’s work: the “cumulative epiphany” (Rhetoric 46), which is a narrative form in which the author comes to understand that the illness has always been a part of who he or she is, and the “dyadic body” (Wounded 35), a word Frank uses to refer to the shared experience of being bodies, in this case bodies who are afflicted with some kind of illness. I will examine these concepts later and refer to them throughout this essay as a means to examine the development and analysis of my personal narrative from a more theoretical perspective. Using these two concepts, I demonstrate how my narrative describes the development of my identity as a person with a disease and how, once I was able to accept that part of myself (particularly with the help of my online friends), I was able to use the medium of narrative to reveal my secret and assimilate the disease into my identity."
"I set the narrative up in short vignettes that pick out specific moments in my life that I felt could best shape the story. My aim was to show how I was born with this disease, rebelled against the life and medical prognosis that comes with a disease such as Cystic Fibrosis, and finally found some kind of peace with myself and the disease through the interactions I had online with other people who also had CF. These online interactions later play a large role in the way I hope to enter my voice into the genre of illness narrative, showing through my personal narrative the way that the internet changes the overall concept of illness writing. Narratives are now being written in real time, updated and changing daily through blogs and social networks as people update continually and interact with others as the disease is happening to them. Through these networks and friendships my personal narrative was shaped. These relationships helped to form my identity as a self with disease because as I read the continuing and ongoing stories of others with my same disease I could relate to them in a way that was not available to me at any other time in my life, either because I rejected it, or because the cross contamination risks of the disease were too great to take the chance of meeting in any other way than in a virtual reality. The relationships served as a mirror of sorts whereby I could compare my disease and myself to others with the same disease and examine how others dealt with their illness and disability, constantly comparing and contrasting that to my own reactions and experiences"
"The idea that life was to be shortened by CF has been a lingering stigma for my entire existence and was a motivating force in my narrative. I wanted to give voice to the deviation my story took as I struggled against this prognostication. I rebelled against the prognosis of CF long before CF made much of an appearance in my life’s narrative. I was rebelling against this “failed prognostication” that had shadowed me for years. In this memoir I’ve presented drug abuse as the primary mode that gave shape to that rebellion. Certainly substance abuse was not the only way I rebelled against my disease, but it is a serious way, and it is an intriguing way given the dire importance good health has in our society, especially when one has a life-shortening disease. Substance abuse is certainly not an issue of childhood and the fact that I was able to get to a point in life with this disease to be able to abuse narcotics is a rebellion of sorts against the disease and the prognostication of where that disease would take me. I should never have been healthy enough to even think about such a lifestyle. I did, however, and then even lived long enough to be able to look back on that time of life and put it to paper. This narrative itself is still a form of rebellion against the prognostication of medicine and society on the illness itself."
This next part is from the personal narrativepart of the project,or the "creative aspect." This is revealing more about me than I probably have to some of you - to others, you know all about this stuff cause you lived this life too. I hope the reader won't judge me too harshly based on how I acted 16 years ago. I am editing slighty, you know, just in case.
1995
She takes a swing and she can’t hit, she don’t mean no harm, she just don’t know what else to do about it
By my senior year of high school I had a handful of friends who had their own places. Bald Jay’s was next to a roachy pizza place on a street infested with hookers, winos, and other denizens of the smarmy South Bend street life. I’m amazed with our bravado in those days. Walking down streets not meant for suburban white girls, preening for the men who cat called, asking for drugs, going into the homes and cars of strangers to get them. I can’t believe we were never hurt; I think of how many ways we were hurt: taken advantage of, exploited, used.
I met Seth eight months after I’d decided to become a born-again virgin. I’d begun to grow weary of the meaninglessness in my interactions with boys. I was seventeen, heading soon for college. I wanted a fresh start; I wanted love. I had succeeded in creating a persona of wild,bad girl, but I started to envy my friends who had boyfriends who bought them flowers and took them on dates. I had visions of a relationship like the romance between Lloyd Dobler and Diane in "Say Anything," of Romeo and Juliet.
That last summer before college, my girlfriends and I had plans to follow the Grateful Dead. We wore second-hand clothes and ate lots of acid. My hair fell to my waist. I carried a one-hitter and a camera in a straw tote bag. I stopped shaving my legs. We were eighteen and free. It was the summer of my first true love.
I remembered Seth from high school. He had twirly eyes, like a cartoon character. I would see those kind of eyes only one time more in my life, in the eyes of a meth head in New Mexico, ironically also named Seth, who wanted a ride. The eyes would scare me. Seth’s eyes scared me. I’d heard the rumors: they all said he was wild. I’d never really paid him much attention until one summer evening at Bald Jay’s.
Like most teenagers’ first apartments, Bald Jay’s was sparsely furnished, the sink always full of dirty dishes. Band posters were tacked about the walls and the company was transient. People who weren’t even really friends with Jay would come by, his house one of the few to hang out in where there were no parents present. Erica and Lola, my closest friends, and I were frequent visitors, being friends with both Bald Jay and one of his roommates. We’d flounce into Jay’s unannounced in our gauzy skirts and sprawl across his couch assuming that our presence was always a welcome addition.
One night Seth slinked into the house and fell into a threadbare chair across from me. His energy was like honey, syrupy sweet. His hair was a tangle of auburn curls. He was shirtless, his chest flat and hard, bare. His army pants were pulled so low that the V of his pelvis was exposed, soft auburn curls peeking from the waistband. He rolled a joint, meticulously folding in the corners of the onion skin paper to make little pockets, then tapping out a sprinkling of cocaine from a magazine folded bindle he kept in the cellophane of his cigarette packet. I wasn’t even sure if he was aware that I was there. We all smoked: Seth and his friend Jake, Bald Jay, Lola, Erica, and I. We passed the joint from fingertip to fingertip, the raucous vibrations of Phish’s “Run like an Antelope” wafting from an upstairs bedroom, the windows open to the humid summer air and the rattling mufflers and loud voices of the downtown street life.
Soon after, Lola, Erica, and I went for a walk on the East Race, a pleasant boardwalk area built around the St. Joseph river. Our gypsy chains jingled, our patchouli drenched skin was soft in the lamplight as we discussed Seth and the cocaine laced joint and whether or not we thought we felt any different from it.
I decided to call Seth “Jim Morrison” in code because of a picture I’d had of the singer on my bedroom wall with the same wild wavy hair and low riding pants. I recruited Erica to help me track him down the next day. We found him on Van Buren Street, in the heart of run down South Bend, lying on a mattress in our friend Ray’s bedroom, smoking a joint. The four of us drove to Rum Village, a park and nature preserve on the southwest side of town, where we swung on the swings and smoked a joint in the woods. Seth massaged my shoulders from the backseat of my car as I drove us back to Ray’s and asked me to come over and go in his hot tub that night. I agreed and snuck out of my house via the sliding glass deck door to meet him at the end of my driveway. He picked me up in his white Honda Civic, a cigarette in hand, Jane’s Addiction on the tape player. My legs glimmered, slathered in the smoothness of Bath and Body works liquid talc....
It was an intense summer. We watched Perry Ferrell shoot up and pretend to be Dr. Rockstar in The Gift. Seth wore my dresses and let me put make-up on him. We had sex in the car, behind a church, in my mother’s house and his father’s, in the woods, in bathrooms. We took Xanax and drank microbrewed beer. We played pool and went to the beach. I was in love. Then he kissed a girl named Vanessa in his hot tub. And the boy I should have let go, of moral failing and intense addiction, I began to cling to even harder. I sobbed the night before I left for college and ate three of my mother’s Xanax bars. My heart was breaking.
When I got to college, still dating Seth long distance, I stopped smoking pot and started taking aerobics. I had the realization that no one was going to look after my health except me. I still drank, took hallucinogens, and did cocaine when we could find it, but I had this grand idea about saving my lungs. I didn’t tell anyone why, I just told them I was “allergic” to marijuana. This was an acceptable answer.
I hung out with hippies, bike thieves, druggies. Of all the people I was friends with in college, only a handful ever finished. Of those who did find success, many took the same roundabout path that I found myself on. The lure of Phish music and freedom was so enticing that working the midnight shift at the BP didn’t seem like a bad gig if it meant you could get all fucked up after and have no responsibility in between. I envied those people. Though I dallied in these fringe groups, I still felt a great deal of pressure to succeed both from my family and intrinsically. I was not going to fail at anything. So I compartmentalized. I could be smart; I could make Dean’s list and still stay up all night on cocaine. I further compartmentalized my CF. I’d left behind most of the people who’d known about it from my childhood, and told fewer and fewer people. I didn’t even tell my college roommate, Maria. Despite being friends in high school, it was several months into living together that one day she noticed me taking medicine before eating and asked me about it. I had no choice except between lying and telling the truth. I opted for the truth. I was embarrassed and played it off as nothing to worry about. I don’t remember telling her about the life expectancy, though I know I often threw that number in, especially as I got older and surpassed it, as a means to prove how unaffected I really was by the disease. A few years later I recall asking Maria about that day and what it was like to live with me during those years.
“Yeah, I do remember when you first told me that you had CF. It was at the very beginning of living in the dorms at BSU. Ryne and I were both there. I think the reason it came up was not about coughing, but as a way to explain why you were taking pills before eating. It was the first time I had ever even heard of CF,” she recalled as we mulled over a bottle of wine.
“I’m sure you told us all about it medically and stuff, but the part I remember most was you saying that most people don't live past 16, which sort of freaked me out. I had never really dealt with the mortality of a close friend. Eighteen is quite an invincible time for most.
“I remember after knowing, feeling protective of you when you would cough... I remember feeling pissed at people who would be like ‘Whoa dude, are you okay!?’ Or, ‘Damn girl, have another cigarette!’ Shit like that, but I would use my lack of concern to try and show them that they were dumb for asking: they should do the same. Looking back, I guess they weren't assholes, just concerned, but I felt sensitive to what I viewed as tactlessness and sort of a MYOB situation.”
Despite not smoking and exercising, two purposeful choices aimed at taking better care of my lung health, I still lived hard. College is a rough time for many coeds; binge drinking and crappy eating are commonplace, and I was no different. I was also warped into an increasingly codependent first love, something akin to a toddler in a Christmas tree shop: excitement, bright lights, and inevitable shattered glass.
Spring semester, Seth followed me to BSU and lived in the same residence hall on the floor below me. We spent most our nights in one another’s rooms. He peed in an empty two liter the nights he spent with me; I lined his trashcan with a plastic bag the nights I spent with him. Though I was modest around his roommate, Maria, Seth, and I were all comfortable with one another and often the three of us slept nude, Maria in her bed, Seth and I crammed into mine talking late into the night. There was something uninhibited about being so uninhibited and I found us all quite bohemian.
I wrote Seth’s papers for him, he rode me to class on the front of his bicycle. For spring break we headed to the Gila Mountains of New Mexico and the peaks of Breckenridge, Colorado with a slight detour to Palomas, Mexico to purchase and smuggle in valium. We both fell in love with the Southwest and vowed to return.
Jealousy had slyly sunk its fangs in our young love over the course of our time together. Less than a year into the relationship we’d both cheated on one another; it’s hard even now to understand why we continued to hang onto each other so fiercely. There was a sexual possession between us that I had never felt before and I wanted no other woman to have my man. It didn’t occur to me then that I wasn’t holding Seth responsible for his transgressions....
Seth transferred to the University of New Mexico the next semester. He and I visited one another each month after he left, once each driving ten hours to meet in Oklahoma for the weekend. I began the paperwork to take out loans to transfer to the University of New Mexico that spring. My parents were vehemently against the idea, Seth becoming nothing more to them than an impediment to my future successes. They truly feared that I would elope or become pregnant by him and bind myself to him even more fully than I already had.
My father, Seth, and I packed up my Toyota Corolla in January of 1997 and drove through the worst snowstorm the southwest had seen in years from Indiana to Albuquerque. My father had succumbed to the fact that he was helpless against me leaving, but he’d at least get me there safely.
The temperature was in the negatives as we drove through the Midwest. Not far out of Indiana we suffered a tear in the sidewall of the tire. Seth and I stood helplessly aside as my father unpacked the entire trunk of the car and attached the spare with his bare and frozen hands. The blowing snow and slippery conditions of the roads as we headed farther south convinced my father that only he should drive and we listened to him lament, “This isn’t good, this isn’t any fucking good” as he inched the car along the Texas highway.
New Mexico quickly became an exercise in addiction. My grades dropped to B’s. Retrospectively, this should have been a warning sign to my parents that something had gone amiss, but a B was still an acceptable grade and no one worried much. The truth was Seth and I spent some days awake on cocaine and some days in a groggy stupor of heroin. My resolve to help him with his addictions dissolved hours after I put my father on a plane back to Indiana.
We made friends with another couple and they were among the first new people I told that I had CF in years. I had no other answer but the truth for why I coughed so incessantly sometimes. Cocaine constricts the nasal passages and some nights the post-nasal drip would cause me to cough and gag without end. As with Maria, Seth was protective of me when someone joked about my coughing. He may have been the one who told them, in all actuality, as a response to some joke such as, “Maybe you need to see a doctor for that cough?”
“What does it taste like?” asked one of the friends. “Is it like when you have a cold?” I had no answer, my sputum always tasted the same; in effect, I always had a cold. I realized that their curiosity wasn’t a bad thing, it wasn’t a force of pity but rather a simple desire to understand. Talking was much easier with the fuel of drug-induced stimulation.
I knew that New Mexico wasn’t a healthy place for me to be. I never saw a doctor when I was there, I did not exercise, I was not eating well. I was clearly abusing drugs. The little cricket voice of my subconscious also knew that starting out my life with thousands of dollars of student loans wasn’t as good an idea as going home and letting my parents pay for my education. Seth scared me as his addiction spiraled farther and farther out of control and I was grasping at twigs trying not to follow him down. It was still important that I remain above water with my school work. The final straw was twofold: a worried phone call from my grandparents one week after we’d unplugged the phone and stayed in bed on a heroin binge, and a family trip to France that was held above me like a carrot on a stick: come home and you can go with us. My choice was made. After one semester and thousands of dollars, I was going back home."
Tuesday, May 24, 2011
down in the boondocks

It's kinda hard to type with this monitor thing on my middle finger.
I'm in the ICU getting desentitized to Fortaz. I totally balked at the idea of coming into the ICU, but it's been great - as great as hospitals can be anyway. I mean, I've gotten my meds on time, my RTs were quite knowledgable about CF, and I slept all night - at least until my nurse woke to tell me by BP was 77 over I dunno what. I think it was a fluke. 77! Makes me wonder WTF happens when I sleep at home! Well and I've got all these damn cords all over. Still, I'll take this over the Oncology floor where I was before n.e. day.
So 10-14 more days of IVs is coming my way, but I'll deal. I want to feel good for our vacation which is rapidly apporaching.
That's about all u have to say. I want to go home!
Thursday, May 5, 2011
Wednesday, May 4, 2011
this is the end, beautiful friend, the end
Today has been a day of endings.
I finished up my last dose of IV Tobra about twenty minutes ago. This is the only time I have ever been on just one IV med and man, is that cake! I am also on inhaled colistin, so it's not like I am on only one med, but still, one infusion BID = sa-weet! So that's done.
That's not all as pie in the sky as I just made it sound, since this was an experiment to see if it would help me before I need to go in and get desensitized to meropenum. er, I guess it's Imipenum. Either way, I haven't heard much good about either med, so I am not really looking forward to that and honestly, I only feel maybe 70% better. I got a stomach virus in the middle of this course of meds that left me with a 102 fever, vomiting, and all together miserable. I feel that it set me a back a bit. Once the fever edged over 100, my heart started beating really hard and my breathing became very labored. I was acutely aware of this, much as I remember I was with H1N1. There is just a point where it seems that my body really begins to struggle with fevers. Maybe everyone's does, I just don't have a whole lot of experience with fevers.
I was thinking today as I was infusing my last med about where I am with my health. In 2007, I weighed 103 lbs and had an FEV1 of 50%. I did no treatments up until that point. Well, no, I guess I had my Vest, because I know I got that soon after my daughter was born. I remember because my boobs were full of milk and it hurt to Vest at first. But anyway, a year later, that's where I was. I feel it's entirely possible, had I not changed that road I was on, that I may not even be here today. Who knows where my health might have been and then to have suffered through the Swine Flu epidemic? yipes. I feel certain it was the grace of god and lungs that cooperated that that didn't hurt my body worse than it did, and I know I lost some lung function over that.
Anyway, I guess that's neither here nor there because I did get compliant and I am still here and I do have a baseline that now hovers around 70 and that is terrific. So I have to remind myself when I reeeaaaalllllyyyy don't want to do IV set #2, complete with some hospital time, that that's just how you have to play this game. If i want to be here for a while longer, I gotta play these cards right.
I really want to be here to see my kids grow up and have kids of their own. I was reading a book to my daughter tonight about a kid that got an ugly knitted sweater from his grandma and I felt deeply how much I want to share that part of life with my kids. It's a realy hard pill to swallow that I might not. Sometimes I can get kind of flippant and even obstinate about it when my family spouts off uber positive thoughts about how possible it is for me to live for a long time more. I feel they are deluding themselves and need to realize the stats are not in my favor. But the truth is, the deep dark truth, is I really would like to be around for a while longer. Facing your own mortality is not easy. I know I am still far enough removed from dying that it solidly remains a "what if" idea. Many people I know are already in end-stage lung disease and I am sure their outlook and wisdom would greatly differ from my own.
I'd come up from the basement earlier tonight when I realized I left the phone down stairs. I asked my son to bring it up to me.
"I'm too tired to come back down" I told him.
"From your thing?" he asked, pointing to my chest. I said yes, that sometimes what's meant to make us better can wear us down a bit first. He called back up the stairs that he hoped they would find a cure soon. This is my son. Somehow squashing my parents' optimism about a cure doesn't seem as unkind as doing it to my son. So I called back, "I don't know that there will ever be a cure, but hopefully they can find something to help me live a long time." By then though he was already immersed back into his Xbox game and I was feeling a little blue.
I digress.
Another ending came as I finished up teaching my 3rd semester in the world of higher learning. I had a failing student complain about me and my "unfair" grading policies to the Dean of my department. She called and asked me if I would be willing to let him take his final exam again. I really debated this. It seemed if I said no, the likelihood of my rehire was small, being an adjunct low on the totem pole. At the same time, I have been trying really hard to be more of a stick-to-my-guns kind of person. What it finally boiled down to was that though I thought that this kid was acting like a spoiled brat, he was entirely capable of doing the work. So to be punitive and fail him based on bureaucratic rules would really be a bit asinine and would probably keep a bright (but slightly annoying) kid from doing something positive with his life. So I let him retake it. It kind of botched up my evening since I had to go in just for that, but he did well and passed the class. So he's done, as am I, for the summer.
I really enjoy teaching at this level. It's pretty unlikely that I will ever go back to full time school teaching, but if I ever do, I am totally holding out to at least get a position in high school. Or even night school, GED. I mean, my dream was to be like "Dead Poet's Society" or something, but it seems I always get thrown in with the lower echelon of studetns, be it skill level or SES or what have you. No matter why, they've sort of become "my people" and I feel I do well by them. So I hope I can continue at this for a while longer.
Finally, in the end of days, I sent my entire master's thesis to my director today. That consisted of 63 pages of narrative and 15 pages of literary context. It took me almost a year to finish it, partly because that's how long it took me, and partly because I had no deadlines and I am working with a very over worked faculty memeber who wasn't always quick on returning my emails and drafts. I am still waiting for her reply, so I may have to edit and revise a bit more, but the bulk of the work is really truly done. Thank goodness! It's such a weight lifted off of me. I will actually get this degree. For a while there it seemed as if it might not happen.
With all that, I leave you with pictures. I just got a new computer and I have a built in camera (so yay! Skype!). I'm only about 10 years behind the rest of the world with my technology. I was just playing with the camera this morning and then again after I finished infusing my last dose of the Tobra.
Enjoy my kewpie looking pictures. (I'd rather be Kewpie looking than Ewok, thank you very much!)





I finished up my last dose of IV Tobra about twenty minutes ago. This is the only time I have ever been on just one IV med and man, is that cake! I am also on inhaled colistin, so it's not like I am on only one med, but still, one infusion BID = sa-weet! So that's done.
That's not all as pie in the sky as I just made it sound, since this was an experiment to see if it would help me before I need to go in and get desensitized to meropenum. er, I guess it's Imipenum. Either way, I haven't heard much good about either med, so I am not really looking forward to that and honestly, I only feel maybe 70% better. I got a stomach virus in the middle of this course of meds that left me with a 102 fever, vomiting, and all together miserable. I feel that it set me a back a bit. Once the fever edged over 100, my heart started beating really hard and my breathing became very labored. I was acutely aware of this, much as I remember I was with H1N1. There is just a point where it seems that my body really begins to struggle with fevers. Maybe everyone's does, I just don't have a whole lot of experience with fevers.
I was thinking today as I was infusing my last med about where I am with my health. In 2007, I weighed 103 lbs and had an FEV1 of 50%. I did no treatments up until that point. Well, no, I guess I had my Vest, because I know I got that soon after my daughter was born. I remember because my boobs were full of milk and it hurt to Vest at first. But anyway, a year later, that's where I was. I feel it's entirely possible, had I not changed that road I was on, that I may not even be here today. Who knows where my health might have been and then to have suffered through the Swine Flu epidemic? yipes. I feel certain it was the grace of god and lungs that cooperated that that didn't hurt my body worse than it did, and I know I lost some lung function over that.
Anyway, I guess that's neither here nor there because I did get compliant and I am still here and I do have a baseline that now hovers around 70 and that is terrific. So I have to remind myself when I reeeaaaalllllyyyy don't want to do IV set #2, complete with some hospital time, that that's just how you have to play this game. If i want to be here for a while longer, I gotta play these cards right.
I really want to be here to see my kids grow up and have kids of their own. I was reading a book to my daughter tonight about a kid that got an ugly knitted sweater from his grandma and I felt deeply how much I want to share that part of life with my kids. It's a realy hard pill to swallow that I might not. Sometimes I can get kind of flippant and even obstinate about it when my family spouts off uber positive thoughts about how possible it is for me to live for a long time more. I feel they are deluding themselves and need to realize the stats are not in my favor. But the truth is, the deep dark truth, is I really would like to be around for a while longer. Facing your own mortality is not easy. I know I am still far enough removed from dying that it solidly remains a "what if" idea. Many people I know are already in end-stage lung disease and I am sure their outlook and wisdom would greatly differ from my own.
I'd come up from the basement earlier tonight when I realized I left the phone down stairs. I asked my son to bring it up to me.
"I'm too tired to come back down" I told him.
"From your thing?" he asked, pointing to my chest. I said yes, that sometimes what's meant to make us better can wear us down a bit first. He called back up the stairs that he hoped they would find a cure soon. This is my son. Somehow squashing my parents' optimism about a cure doesn't seem as unkind as doing it to my son. So I called back, "I don't know that there will ever be a cure, but hopefully they can find something to help me live a long time." By then though he was already immersed back into his Xbox game and I was feeling a little blue.
I digress.
Another ending came as I finished up teaching my 3rd semester in the world of higher learning. I had a failing student complain about me and my "unfair" grading policies to the Dean of my department. She called and asked me if I would be willing to let him take his final exam again. I really debated this. It seemed if I said no, the likelihood of my rehire was small, being an adjunct low on the totem pole. At the same time, I have been trying really hard to be more of a stick-to-my-guns kind of person. What it finally boiled down to was that though I thought that this kid was acting like a spoiled brat, he was entirely capable of doing the work. So to be punitive and fail him based on bureaucratic rules would really be a bit asinine and would probably keep a bright (but slightly annoying) kid from doing something positive with his life. So I let him retake it. It kind of botched up my evening since I had to go in just for that, but he did well and passed the class. So he's done, as am I, for the summer.
I really enjoy teaching at this level. It's pretty unlikely that I will ever go back to full time school teaching, but if I ever do, I am totally holding out to at least get a position in high school. Or even night school, GED. I mean, my dream was to be like "Dead Poet's Society" or something, but it seems I always get thrown in with the lower echelon of studetns, be it skill level or SES or what have you. No matter why, they've sort of become "my people" and I feel I do well by them. So I hope I can continue at this for a while longer.
Finally, in the end of days, I sent my entire master's thesis to my director today. That consisted of 63 pages of narrative and 15 pages of literary context. It took me almost a year to finish it, partly because that's how long it took me, and partly because I had no deadlines and I am working with a very over worked faculty memeber who wasn't always quick on returning my emails and drafts. I am still waiting for her reply, so I may have to edit and revise a bit more, but the bulk of the work is really truly done. Thank goodness! It's such a weight lifted off of me. I will actually get this degree. For a while there it seemed as if it might not happen.
With all that, I leave you with pictures. I just got a new computer and I have a built in camera (so yay! Skype!). I'm only about 10 years behind the rest of the world with my technology. I was just playing with the camera this morning and then again after I finished infusing my last dose of the Tobra.
Enjoy my kewpie looking pictures. (I'd rather be Kewpie looking than Ewok, thank you very much!)





Wednesday, March 23, 2011
she's a good hearted woman in love with a good timing man
I love me some "old" country. I use the term "old" loosley, as I mean "old" as even up to the nineties - before country became the top 40 popular, trendy genre it's becoming now. I mean, I saw Faith Hill at the 4H fair in about 1996 long before Faith Hill was known for much of anything. And that's not to say I don't occasionally hear a new song that I like, it's just that tunes such as "Honkey Tonk Badonkadonk" or "She Thinks my Tractor's Sexy" just don't pull on me the way a little Hank Williams, sr. or jr., can or the way Crystal Gayle singing "Don't it Make my Brown Eyes Blue" does.
As a kid my dad used to listen to country music when he'd make us lunch. This was when I was really young. My dad made this sandwich called a "veggie special" in which he took a piece of whole wheat bread, spread some pizza or spaghetti sauce on it, put a little wheat germ on top of that, added some frozen mixed vegetables and then topped it off with a slice of American cheese. Into that new contraption called a microwave it went, and yum yum.
My parents were newly divored and though my dad was definitely the more health conscious of my two parents (hence the wheat germ. We also ate carob, weren't allowed gum with sacchirine in it and visited the Mekong Market where he bought little glass vials of ginseng which he called "Kra-teen Daaang" (sp)), he wasn't as much of a chef as my mother. As we sat at the table and waited for him to make the veggie specials, he would turn the little radio on in the kitchen to an AM country station. I can still hear him singing "Texas weh-eh-men" in a low baritone.
My dad introduced me to a lot of different types of music and for that I am really grateful. He did his Master's thesis on music ethnography in which he wrote about the blues. I assume thisa was when his vast study of music really started. The music of my childhood ranged from the reggae beats of Bob Marley, Peter Tosh, or Burning Spear to the wailing guitars of the Kings: B.B., Freddie, and Albert. Some days it was the jazzy sounds of Gato Barbieri, Wes Montgomery, or Miles Davis. I heard the bizarre sounds of Sun Ra and the melodic Augustus Pablo (I wanted to name my daughter Augustus or August if she was a boy and call her Gus. Augustus was influenced by melodian player Augustus Pablo and August was influenced by the Grateful dead song "Wharf Rat": "My name is August West and I love my pearly baker best more than my wine")).
My dad was a big Beatles fan so there was no shortage of them or the Rolling Stones or Cream and other music of the sixties and seventies. Other names that come to mind are Bloomfield Cooper and Savoy Brown, Leon Russell, Santana, Howlin' Wolf, and Charlie Parker. I remember on Friday nights we would go to dinner and then rent a movie (the VCR was also a new thing at this time). We watched Movies like "Bird" and "Crossroads." Clearly, my childhood musical education did not suffer. My dad was making mixed tapes from his record player waay back in the day. And so, in the afternoon we'd listen to country music.
When I met my husband he introduced me to a new subculture, one I had not really been privvy to in my middle class (maybe even upper middle class? I'm not sure where the class lines divide, really) upbringing: that of the "working man."
My father was an academic, my mother in social work, and my step mother a physician. My grandfather was Vice President of an Insurance company on one side and the other worked for a short time as a Foreign relations represenative for a local company that made materials used in WW II. That grandfather was from a small farm community rife with Amish called Nappanee. So for all our "worldliness" (my grandmother was the daughter of a diamiond cutter and grew up in South Africa) there was always that tinge of good old farm folk within us. Still, I knew relatively nothing about the world of the skilled trades and construction. My knowledge of construction was basically the stereotypical guy eating his lunch from a metal box sitting up high on the beam of developing building and whistling at women as they passed the site. G showed me that most of what I sterotyped wasn't true and I found great comfort and happiness with his friends and family. It was an easy integration of lifestyles and we found enjoyment on both ends of our spectrum.
G came from a family of brick layers. His grandfather, father, and both brothers were in the trade. G branched out and chose plumbing/pipefitting rather than bricklaying and much of this was due to the training he recived when he was in the Navy. His maternal grandfather had also been a Navy man though I don't know what career he had after that.
When I met my G I wasn't just introduced to this "blue collar" world, but along with that some new music. I started listening to Waylon and George Jones, Hank jr., Lynrd Skynrd, The Allman Brothers and The Marshall Tucker Band: Outlaw country and Southern Rock. It wasn't that i didn't know who most of those musicians were, only that I hadn't really listened to them. My dad had once forced me as a teenager to go and hear The Charlie Daniels Band one year when they came to the county fair. "It's Charlie Daniels, man!" he exclaimed. "You can't miss an opportunity to hear Charlie Daniels. I went reluctantly, but groused the whole time.
By the time I'd met my husband at age twenty three I'd formed my own musical taste, influenced by my upbringing and incorporated with my own preferred styles: folky rock, alt-country, and folky punk.
On one of our first dates my (not yet) husband and I went to a concert to hear Deep Purple, Ted Nugent, and Skynrd. Though not much of a fan of Nugent and Deep Purple, I really enjoyed hearing Skynrd. It wasn't the original band, but at that time there were still three of the original members. I'd been listening to quite a bit of classic rock in the time before I'd met my husband and had taken quite a liking to the Eagles and Bob Seger. My husband had a motorcycle when we met and Seger especially seemed to go hand in hand with this new guy: my pipe fitting Harley riding (soon-to-be) husband and this very exciting new romance.
After a few years together and my husband and I getting an ipod, I really took to the outlaw country. He had a lot of CDs I had never even heard until they were downloaded into the itunes. These songs were of hard working, hard drinking men and their tough and loyal wives. I felt as if G and I fit right into the mold of the stories told in those songs. Especially after out daughter was born and I was no longer spending as much time outlawing it with him as I was home with our baby. I truly felt I was becoming the like the women who sang and were in the songs.
The sad thing is, as much as I enjoyed it, I can't really listen to that music much any more. It has become too painful. I don't want to be married to an Outlaw and I don't want to be a woman who is singing about fighting for her man. It's funny that Hank Williams jr.'s song "Women I've Never Had" used to make me smile. Now it sort of makes me sick. "Jackson" makes me angry. Hearing "Whiskey Bent and Hellbound" is liable to give put the urge on me to put my fist through something much like Loretta's, "Fist City," though I can't listen to that one much either. Willie's songs still pull on my heart strings but they hurt too. I don't want to be the good hearted woman any longer.
I've been searching for songs that speak to who I am and where I am right now. As a teenager I used to play a game where someone would give me a word and I would come up with a song lyrics to go with it. I always said "life is a medley." Nowadays my motto has been more "music is god" and I've taken to letting the shuffle on the ipod teach me whatever lesson I am supposed to learn for the day. I'm trying to believe that things happen as they should and that I can only control so far as the end of my nose. That's left me adrift in the musical world. Despite all the music I've been introduced to in my life, I can't find a fit right now. I don't quite see myself heading into the Chritian rock arena though I suppose a song called "In His Hands" could work for me if it was perhaps renamed to something like "Wrapped up in the Energy of the Universe." and I bet that song exists somewhere too, though it's probably being chanted by a bald New Yorker who dropped out of Julliard to live in a Indian Ashram while his grandmother paid off his student loans for him.
My point about the music may have been lost, but what I'm trying ot say is that I am adrift right now and I am looking for an anchor or an identity. The previous nine weeks have made me reevaluate who I am, what I believe, and how I see myself. I can't find a song to identify with right now.
I am starting to believe that there is purpose in life that isn't always obvious as events are unfolding (maybe I always believed that, but it seems really obvious to me now). I'd like to think that my days spent as the faithful Outlaw wife had meaning and that the catastrophe that unfolded around me two months ago might just have been the answer to my prayers (and how fucked up is that anyway? if everything happens for a reason then the universe is one ironic fuck up of a place). If this is true, then I hope at some point I can listen to Waylon and Jessi singing "I ain't the one" again without breaking down. that I might once again enjoy crooning along with Hank about my wild friends that have settled down because I will be one of them. I may not identify in the same way with the music, but I won't have to shut it or certain parts of my life out of my mind because of all the hurt.
I'd like to imagine the broken pieces of my life settling into a compact pile of debris that's busy making diamonds under the pressure. If life happens as it should, and I can imagine a celestial hand holding me gently through it all, then I know every time things seem the most dire I will be eable to unearth one of those diamonds and find the beauty that comes from disaster.
If it happens as it's supposed to, then I can still hang on to Willie crooning, "If you had not fallen then I would not have found you, Angel flying too close to the ground." and all will not be lost with who I was but only that more is to be gained with who I am in the now.
(I totally apologize if this isn't all that coherent. I've worked on it off and on all day amid interuption after interuption and I just want to be done with it - so off to the internets it goes!)
As a kid my dad used to listen to country music when he'd make us lunch. This was when I was really young. My dad made this sandwich called a "veggie special" in which he took a piece of whole wheat bread, spread some pizza or spaghetti sauce on it, put a little wheat germ on top of that, added some frozen mixed vegetables and then topped it off with a slice of American cheese. Into that new contraption called a microwave it went, and yum yum.
My parents were newly divored and though my dad was definitely the more health conscious of my two parents (hence the wheat germ. We also ate carob, weren't allowed gum with sacchirine in it and visited the Mekong Market where he bought little glass vials of ginseng which he called "Kra-teen Daaang" (sp)), he wasn't as much of a chef as my mother. As we sat at the table and waited for him to make the veggie specials, he would turn the little radio on in the kitchen to an AM country station. I can still hear him singing "Texas weh-eh-men" in a low baritone.
My dad introduced me to a lot of different types of music and for that I am really grateful. He did his Master's thesis on music ethnography in which he wrote about the blues. I assume thisa was when his vast study of music really started. The music of my childhood ranged from the reggae beats of Bob Marley, Peter Tosh, or Burning Spear to the wailing guitars of the Kings: B.B., Freddie, and Albert. Some days it was the jazzy sounds of Gato Barbieri, Wes Montgomery, or Miles Davis. I heard the bizarre sounds of Sun Ra and the melodic Augustus Pablo (I wanted to name my daughter Augustus or August if she was a boy and call her Gus. Augustus was influenced by melodian player Augustus Pablo and August was influenced by the Grateful dead song "Wharf Rat": "My name is August West and I love my pearly baker best more than my wine")).
My dad was a big Beatles fan so there was no shortage of them or the Rolling Stones or Cream and other music of the sixties and seventies. Other names that come to mind are Bloomfield Cooper and Savoy Brown, Leon Russell, Santana, Howlin' Wolf, and Charlie Parker. I remember on Friday nights we would go to dinner and then rent a movie (the VCR was also a new thing at this time). We watched Movies like "Bird" and "Crossroads." Clearly, my childhood musical education did not suffer. My dad was making mixed tapes from his record player waay back in the day. And so, in the afternoon we'd listen to country music.
When I met my husband he introduced me to a new subculture, one I had not really been privvy to in my middle class (maybe even upper middle class? I'm not sure where the class lines divide, really) upbringing: that of the "working man."
My father was an academic, my mother in social work, and my step mother a physician. My grandfather was Vice President of an Insurance company on one side and the other worked for a short time as a Foreign relations represenative for a local company that made materials used in WW II. That grandfather was from a small farm community rife with Amish called Nappanee. So for all our "worldliness" (my grandmother was the daughter of a diamiond cutter and grew up in South Africa) there was always that tinge of good old farm folk within us. Still, I knew relatively nothing about the world of the skilled trades and construction. My knowledge of construction was basically the stereotypical guy eating his lunch from a metal box sitting up high on the beam of developing building and whistling at women as they passed the site. G showed me that most of what I sterotyped wasn't true and I found great comfort and happiness with his friends and family. It was an easy integration of lifestyles and we found enjoyment on both ends of our spectrum.
G came from a family of brick layers. His grandfather, father, and both brothers were in the trade. G branched out and chose plumbing/pipefitting rather than bricklaying and much of this was due to the training he recived when he was in the Navy. His maternal grandfather had also been a Navy man though I don't know what career he had after that.
When I met my G I wasn't just introduced to this "blue collar" world, but along with that some new music. I started listening to Waylon and George Jones, Hank jr., Lynrd Skynrd, The Allman Brothers and The Marshall Tucker Band: Outlaw country and Southern Rock. It wasn't that i didn't know who most of those musicians were, only that I hadn't really listened to them. My dad had once forced me as a teenager to go and hear The Charlie Daniels Band one year when they came to the county fair. "It's Charlie Daniels, man!" he exclaimed. "You can't miss an opportunity to hear Charlie Daniels. I went reluctantly, but groused the whole time.
By the time I'd met my husband at age twenty three I'd formed my own musical taste, influenced by my upbringing and incorporated with my own preferred styles: folky rock, alt-country, and folky punk.
On one of our first dates my (not yet) husband and I went to a concert to hear Deep Purple, Ted Nugent, and Skynrd. Though not much of a fan of Nugent and Deep Purple, I really enjoyed hearing Skynrd. It wasn't the original band, but at that time there were still three of the original members. I'd been listening to quite a bit of classic rock in the time before I'd met my husband and had taken quite a liking to the Eagles and Bob Seger. My husband had a motorcycle when we met and Seger especially seemed to go hand in hand with this new guy: my pipe fitting Harley riding (soon-to-be) husband and this very exciting new romance.
After a few years together and my husband and I getting an ipod, I really took to the outlaw country. He had a lot of CDs I had never even heard until they were downloaded into the itunes. These songs were of hard working, hard drinking men and their tough and loyal wives. I felt as if G and I fit right into the mold of the stories told in those songs. Especially after out daughter was born and I was no longer spending as much time outlawing it with him as I was home with our baby. I truly felt I was becoming the like the women who sang and were in the songs.
The sad thing is, as much as I enjoyed it, I can't really listen to that music much any more. It has become too painful. I don't want to be married to an Outlaw and I don't want to be a woman who is singing about fighting for her man. It's funny that Hank Williams jr.'s song "Women I've Never Had" used to make me smile. Now it sort of makes me sick. "Jackson" makes me angry. Hearing "Whiskey Bent and Hellbound" is liable to give put the urge on me to put my fist through something much like Loretta's, "Fist City," though I can't listen to that one much either. Willie's songs still pull on my heart strings but they hurt too. I don't want to be the good hearted woman any longer.
I've been searching for songs that speak to who I am and where I am right now. As a teenager I used to play a game where someone would give me a word and I would come up with a song lyrics to go with it. I always said "life is a medley." Nowadays my motto has been more "music is god" and I've taken to letting the shuffle on the ipod teach me whatever lesson I am supposed to learn for the day. I'm trying to believe that things happen as they should and that I can only control so far as the end of my nose. That's left me adrift in the musical world. Despite all the music I've been introduced to in my life, I can't find a fit right now. I don't quite see myself heading into the Chritian rock arena though I suppose a song called "In His Hands" could work for me if it was perhaps renamed to something like "Wrapped up in the Energy of the Universe." and I bet that song exists somewhere too, though it's probably being chanted by a bald New Yorker who dropped out of Julliard to live in a Indian Ashram while his grandmother paid off his student loans for him.
My point about the music may have been lost, but what I'm trying ot say is that I am adrift right now and I am looking for an anchor or an identity. The previous nine weeks have made me reevaluate who I am, what I believe, and how I see myself. I can't find a song to identify with right now.
I am starting to believe that there is purpose in life that isn't always obvious as events are unfolding (maybe I always believed that, but it seems really obvious to me now). I'd like to think that my days spent as the faithful Outlaw wife had meaning and that the catastrophe that unfolded around me two months ago might just have been the answer to my prayers (and how fucked up is that anyway? if everything happens for a reason then the universe is one ironic fuck up of a place). If this is true, then I hope at some point I can listen to Waylon and Jessi singing "I ain't the one" again without breaking down. that I might once again enjoy crooning along with Hank about my wild friends that have settled down because I will be one of them. I may not identify in the same way with the music, but I won't have to shut it or certain parts of my life out of my mind because of all the hurt.
I'd like to imagine the broken pieces of my life settling into a compact pile of debris that's busy making diamonds under the pressure. If life happens as it should, and I can imagine a celestial hand holding me gently through it all, then I know every time things seem the most dire I will be eable to unearth one of those diamonds and find the beauty that comes from disaster.
If it happens as it's supposed to, then I can still hang on to Willie crooning, "If you had not fallen then I would not have found you, Angel flying too close to the ground." and all will not be lost with who I was but only that more is to be gained with who I am in the now.
(I totally apologize if this isn't all that coherent. I've worked on it off and on all day amid interuption after interuption and I just want to be done with it - so off to the internets it goes!)
Labels:
grief,
healing,
husband,
love,
motorcycles,
music,
pain,
random musings,
understadning
Friday, March 4, 2011
I heard the news today oh boy
Yesterday my husband and I did a "Day in the Life." Well, mostly I did it, but he was in on the gig. I noticed a few main things while looking at the pics I was going to use:
1) my son is missing from all pictures. I think this is mostly because he left for school before I got up, he came home after school and immeciately went to play with his friends, and then when he was here hanging out, I was busy grading papers and the like. Anyway, sorry mijo.
2) I had clinic today which I took no pictures of. I felt wierd going in to my clinic and snapping pics. I was going to take a pic of the outside of the bulding and a few inside the exam room, like of my sputum cup or something, but I forgot. So I snapped a picture of my PFT print out when I got home. (FEV1 was 72 and I hadn't even done a treatment yet that day, so that's great (though 25/75 was 26, so clearly there is a big discrepancy there and that's where the treatments are really making the difference (the highest I've seen that in years is 39 and I think that was post IVs)).
3) I went out and had a cocktail with a friend and didn't snap any pics there either. It would have been proof I actually do have IRL friends! I'm not the cyber loner I come across as. :) I'm just a picture loser. But she doesn't know I have this blog and I wasn't ready to explain it yet (she does know I have CF though), so just enjoyed my "pom peche" martini and let the camera rest.
Point being: lots of holes in this DITL, so I guess in a way, it isn't represenative of my life fully at all. C'est la vie, n'est pas?
oh, and 4)I might have a broken nose. The baby I sit for head butted me last week. You can see the line where my glasses hit against my face and my nose is pretty swollen near the bridge. It's ooogly. I surely wasn't thinking this was going to be my most beautiful day when I decided to do this DITL!

Gregg is up and getting ready to start the day's project while I take Miss M to school: tamales!

Miss M busted trying to feed the dog cheerios.

This is how I look in the morning. With a busted face. sca-wee!

Off to school!

Picking up cumin, chili powder, black pepper, and some candy (not for the tamales, for mah belleh).

corn husks a-soakin'

cerdo tirado!

We had to set the tamale makin' mood

sneaking a pic of my man lathering up

picking up Miss M from school. I think my car needs a wash.

Nothing sweeter than seeing the preschoolers coming out of the school doors. Melts my heart everytime.

cleaning up puppy pee. When will he be trained??

My girl

Posing with my tamales before devouring more than I want to admit to

Hot tamale baby! Who knew food would be such an important part of this day?

PFTs

Gregg and his pup

The pup. Gregg took this pic. He is a far better photographer than I am, but I can't get the camera into his hands enough.

Trying to get Slugger to wake Marls from her siesta

"I don't wanna get up!"

The dog says, "Why do you people always make me do the dirty work?"

Back to sleep for a bit.

I told Gregg to take a picture of me that captured his love for me

This is it: the picture of love.

My chores. Laundry. I don't mind putting it in the washer, I don't mind taking it out. I HATE folding it, and I ABHOR putting it away. Give me a toilet brush any day, seriously.

Getting ready to have a cocktail with a friend Hair down?

Or up?

The meeting place for the alcoholic debauchery.

I came home and Gregg and his friend were watching youtube videos. The friend pulled up some beheading clip. I told G not to watch it. I told him. He watched anyway and was disturbed and upset for the rest of the night. Sometimes I have to say it: I told you so. I did not watch nor listen to such a video. Just thinking about it makes me ill.

Face washed, contacts out. Back-to-normal Shan.

Trying to get a pic of nekkid G. Undies are close enough. He might kill me for posting this. It may disappear.

good night moon. good night dog.

scrub a dub dub

Gregg and I taking a nighty night pic

I told him we should make out in front of the camera

we were laughing about this and I started to cough when he went to take the pic so I covered my mouth - partly out of polite habit, partly because I didn't want an ugly red faced coughing pic on here.

I told Gregg to kiss me. This was his reaction.

Got him to smooch me anyway. <3
1) my son is missing from all pictures. I think this is mostly because he left for school before I got up, he came home after school and immeciately went to play with his friends, and then when he was here hanging out, I was busy grading papers and the like. Anyway, sorry mijo.
2) I had clinic today which I took no pictures of. I felt wierd going in to my clinic and snapping pics. I was going to take a pic of the outside of the bulding and a few inside the exam room, like of my sputum cup or something, but I forgot. So I snapped a picture of my PFT print out when I got home. (FEV1 was 72 and I hadn't even done a treatment yet that day, so that's great (though 25/75 was 26, so clearly there is a big discrepancy there and that's where the treatments are really making the difference (the highest I've seen that in years is 39 and I think that was post IVs)).
3) I went out and had a cocktail with a friend and didn't snap any pics there either. It would have been proof I actually do have IRL friends! I'm not the cyber loner I come across as. :) I'm just a picture loser. But she doesn't know I have this blog and I wasn't ready to explain it yet (she does know I have CF though), so just enjoyed my "pom peche" martini and let the camera rest.
Point being: lots of holes in this DITL, so I guess in a way, it isn't represenative of my life fully at all. C'est la vie, n'est pas?
oh, and 4)I might have a broken nose. The baby I sit for head butted me last week. You can see the line where my glasses hit against my face and my nose is pretty swollen near the bridge. It's ooogly. I surely wasn't thinking this was going to be my most beautiful day when I decided to do this DITL!
Gregg is up and getting ready to start the day's project while I take Miss M to school: tamales!
Miss M busted trying to feed the dog cheerios.
This is how I look in the morning. With a busted face. sca-wee!
Off to school!
Picking up cumin, chili powder, black pepper, and some candy (not for the tamales, for mah belleh).
corn husks a-soakin'
cerdo tirado!
We had to set the tamale makin' mood
sneaking a pic of my man lathering up
picking up Miss M from school. I think my car needs a wash.
Nothing sweeter than seeing the preschoolers coming out of the school doors. Melts my heart everytime.
cleaning up puppy pee. When will he be trained??
My girl
Posing with my tamales before devouring more than I want to admit to
Hot tamale baby! Who knew food would be such an important part of this day?
PFTs
Gregg and his pup
The pup. Gregg took this pic. He is a far better photographer than I am, but I can't get the camera into his hands enough.
Trying to get Slugger to wake Marls from her siesta
"I don't wanna get up!"
The dog says, "Why do you people always make me do the dirty work?"
Back to sleep for a bit.
I told Gregg to take a picture of me that captured his love for me
This is it: the picture of love.
My chores. Laundry. I don't mind putting it in the washer, I don't mind taking it out. I HATE folding it, and I ABHOR putting it away. Give me a toilet brush any day, seriously.
Getting ready to have a cocktail with a friend Hair down?
Or up?
The meeting place for the alcoholic debauchery.
I came home and Gregg and his friend were watching youtube videos. The friend pulled up some beheading clip. I told G not to watch it. I told him. He watched anyway and was disturbed and upset for the rest of the night. Sometimes I have to say it: I told you so. I did not watch nor listen to such a video. Just thinking about it makes me ill.
Face washed, contacts out. Back-to-normal Shan.
Trying to get a pic of nekkid G. Undies are close enough. He might kill me for posting this. It may disappear.
good night moon. good night dog.
scrub a dub dub
Gregg and I taking a nighty night pic
I told him we should make out in front of the camera
we were laughing about this and I started to cough when he went to take the pic so I covered my mouth - partly out of polite habit, partly because I didn't want an ugly red faced coughing pic on here.
I told Gregg to kiss me. This was his reaction.
Got him to smooch me anyway. <3
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