Sunday, September 1, 2019

I went Skydiving. Also, my health is crap.

Early morning phone calls from the head of your medical team are never a good sign. It what something like this, "It is imperative, vital, that you begin treatment immediately. I am... worried about you." Not many things shake me to my core, this is one of them. I have spent the last two months deteriorating, but also, living. I made my skydive on Aug 28th, to the dismay of pretty much my entire team. Luckily, my specialist understands that happiness is as much of a "treatment" as anything else and signed my waiver when none of my other physicians would. I am incredibly grateful to have him. The experience will stay with me forever. P.s Sorry for the title. I was too tired to be punny.


I would be lying if I said my health hasn't taken a huge hit since July. It's odd. I had this idea of what my second time around with this disease would be like. I thought my progression would move just as slow, if not slower, than the first time around. I figured I would have plenty of time to keep doing the things I love, like working. I also figured I would treat more naturally this time around. Using homeopathic remedies and life style adjustments, like cleaner everyday products, detoxifications, and supplements, instead of prednisone and immune suppression. I figured it would be easier because I knew what to expect. That I would somehow handle it better. Unfortunately, my body has made it very apparent, that any idea I had was wrong. I have declined faster than my doctors or I expected.

My lungs have recently been showing signs of disease. I've noticed shortness of breathe with physical exertion and increasing sleep issues... which of course makes everyday life extremely challenging. Sleep for someone like me is vital. My team is desperately trying to get me scheduled for a sleep study to get my Bipap prescription and levels renewed, but clinics in my area are booked out for months. (Apparently everyone truly is Sleepless in Seattle lol) The level of exhaustion during the day has reached a point where I am simply not functioning. I can't focus or stay awake, the bags under my eyes have their own bags, and driving to work has honestly become unsafe. I've had to completely cut out aerobic exercise and have a very difficult time with stairs right now. My muscles ache and I feel myself struggling to get a breath, often resulting in headaches if I push myself too far. My pulmonologist, who is booked clean into mid September, decided I couldn't wait to be evaluated and sent me to my PCP for a six minute walk study. I began to desaturate once we picked up our walking pace - with O2 levels hovering just below 90. They both concluded that my current lung issues cannot wait until mid September and gave me a referral to see one of their mutual associates who can see me sooner. They also scheduled me for PFTs at two different clinics in hopes that one will have a cancellation for an earlier appointment, as well as an HRCT to get a view of exactly what's happening inside my lungs. For the time being I am to, "avoid physical activity above a brisk walk..." Um what? I have stairs into my apartment, I have stairs at work, I frequently go to the gym, and I enjoying being out in nature! My life is pretty much always more involved than a brisk walk.

On the GI side of things, I've been dealing with a plethora of stoma issues. I had to have a large abscess drained on the left side of my stoma recently. Abscesses can be extremely dangerous and must be monitored closely. Thankfully, after the infection was drained the wound has almost completely healed. As abscesses have a high rate of reoccurrence, I am under carful watch. My SIBO has been absolutely intolerable. It took my insurance company nearly 6 weeks to finally approve the necessary medication! Thankfully I've been doing much better since we started the constant dosing of Xifaxan. I am still struggling to gain any weight and am unable to reach above 139lbs, even with 2,000 calories a day of formula. The idea of, "recreational eating" has been almost a complete bust. At this point my effort is in simply drinking more than only water without feeling horribly sick... My team had hoped many issues such as brain fog and hair loss were related to nutritional issues, however, that was deemed inaccurate. My latest blood panels seemed to be within reasonable nutritional levels for someone on tube feeds, yet my fog and hair loss continues. They now believe it is all simply related to this progressive flare I am experiencing.

Pain. Where to even begin. Exhaustion and pain are a never ending cycle. Being in constant pain is absolutely exhausting, that exhaustion leads to more pain, which leads to further exhaustion, etc. Every muscle in my body aches, every nerve is on fire, and every inch of me is screaming. I am struggling to leave my bed every morning, and when I do, I find myself back in it in a few hours. The feeling you get after being up for 48 straight hours, that delirious level of fatigue, is currently my baseline.

After the phone call from my doctor, and the last month of existing in my body, I have realized two things:
  1. I cannot continue like this.
  2. If I want to survive I need to make some very tough choices. 
Everything within me is pushing against these choices. My feet are digging into the proverbially ground, desperately trying to defy what has to be done - but my legs are too weak to hold out. I've spent more time in the last month crying than I have in a very long time. I feel like I've lost again. Lost my autonomy. No matter how desperately I want to, "get out and live a normal life," I cannot force my body to do so. I cannot pretend to continue on like I am not sick. Like I don't need doctors or treatment. I cannot wake up and go to work every day. I can hardly get out of bed let alone get ready, get in a car, sit in traffic, and work an 8 hour shift managing multiple employees. So, to address number one and number two, I will cutting my hours back from 40 hours a week to 18. I am hoping this will give my body enough time to rest and recuperate between work days. I will also be starting treatment; Rituxan. I have done Rituxan in the past many times and feel it is the, "easiest of all the evils" I have experienced, however, it is also highly effective. This is the absolute last thing I want to do, but I know that continuing to work a full time job, as well as neglecting treatment, will only destroy my body faster.

I am miserable. I can only hope that giving myself more time to rest and beginning treatment will improve my circumstances soon. Thank you to everyone who has stuck with me on this crazy teeter-totter ride! For more info and photos regarding my skydive, please check out my instagram @thetubefedwife

11 comments:

  1. Glad you got to go sky diving, you are much braver than I. Prayers the Rituxan and decreased work schedule provide relief!

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  2. My Mom always said she wanted to sky but never did. You look like you had a blast. Picture made me smile. I'm sorry you have had more health issues arise. I love your attitude even though things are so unfair. I'll pray you got some relief soon. Annette

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  3. I am heartbroken to hear this update. I had so wished this transplant would be a cure for you. Damn disease! I know medical advice is a dime a dozen, so take it or leave it��, but my dear friend with EDS had SIBO and ended up doing an FMT at Virginia mason. It worked well and the latest research on it is very promising! You might check it out. If you ever need a contact, let me know.
    - Heidi Marsh

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  4. So glad you went skydiving!! sometimes you have to say 'what the $%^&" and do the thing! I am sad to hear you are declining, but stay hopeful, maybe this really is just a 'flare' and will be better in a month or two after having some treatments and rest. Rest...others just don't always get it, my daughter was complaining about me not doing the grocery shopping much anymore, you know how hard that is to get out and do?! ha, praying for your 'flare' to be over soon and you can not be in full body pain. Sue

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  5. I am in Va and diagnosed with undifferentiated connective tissue disease in 2014. My insides do not match my outsides now. So I know what your post means about sleep and pain and fatique. Happy your insurance company is covering this now. And that sky diving smile will take you thru future challenges. Make it your screen saver.

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  6. Your strength is inspiring. You are amazing. I love that you will leave no stone unturned. If you can, you might like to borrow this book from your library: Mental Sharpening Stones by Jeffrey N. Gingold. It contains helpful passages on: pacing, fatigue, and embracing disease. Please know that you are not alone. I'll find you on FB via messenger. Hang in there, and please rest when you can. /s

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  7. Dear Chanel, your title for this post is perfect, it is Honest.
    I can only imagine how difficult this is for someone of your tender years. I continue to pray that your pain will be lessened and your strength of spirit increased. I Love You as if You were my own child, or Grandchild. And there are thousands of others who Love You Unconditionally, so you are never alone.
    I am Grateful that you are in my life, and Grateful that you are sharing your's. Thank You Little One! Much Love, Many Blessings and Gratitude and Joy Xoxox Hugs Namaste ❤❤❤❤❤❤❤❤

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  8. You are an heroic woman. Just remember when you feel helpless that you are no different than the infant Jesus. Rest, cry, laugh, mourn....all are fitting responses to the painful existence you are NOT enduring, rather....you are living every moment.

    You have spread your gifts far and wide and graced my life with your giving nature. Thank you!

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  9. Hi, I am so sorry for what you are going through. I’m a case manager for a non profit with people who also have a chronic illness or disability. I also live in the Seattle area. I can’t even begin to imagine what you are going through. I would love to help in any way possible, wether it’s helping you run some errands or cleaning.

    Please let me know.

    Sending you the best healing and positive vibes.

    Richie

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  10. Hi Channel! Rest and do your treatment,and meanwhile let your mind go back to Skydive and imagine doing it with all of us,together,flying,feeling free and happy,with the wind singing in our ears ...sending you all the love and all the hugs that I have❤️ be brave ❤️

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