Dec 11, 2024
The worst part about being chronically ill is constantly feeling like you are unworthy of love.
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The worst part about being chronically ill is constantly feeling like you are unworthy of love.
Anya is live and ready to show you everything. Watch her strip, dance, and perform exclusive shows just for you. Interact in real-time and make your fantasies come true.
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The hardest part of coming to terms with having an autoimmune disease for me has been recognizing and accepting that I can no longer do everything I want to do. Nor everything I may want to do in the future. I can't have it all anymore. I have to choose.
I know that people aren't here for my real life situation, but I'm back in hospital (a different and better hospital) for more Ivig treatment, I know the writing says 24/06/24 but the cannula was put in my hand yesterday
I just wanted to let you guys know where I've been for the last 3 years. This video explains everything. I also want you all to know that I have missed you and want to start working on stuff again but it's going to take time.
That all being said I have released some new merch. It's some cool stuff if I do say so myself. (Though I might be a little biased.) I hope you all enjoy it as much as I enjoyed making them.
$11k
I had $11,000.00 of medicine (IVIg) in my refrigerator last night. Now, after a 5-hour infusion, it is in my son. This happens every 10 weeks.
I have insurance, of course. And at this point in the year, no matter how high, we've met the deductible. So it is "free" for some definition of the word.
If we were ever to lose our insurance, we could probably keep treating him for a couple or few years before we'd lose our house and all of our savings. We'd be homeless, and he'd be in a wheelchair.
It's a sobering thought.
Anya is live and ready to show you everything. Watch her strip, dance, and perform exclusive shows just for you. Interact in real-time and make your fantasies come true.
Free to watch • No registration required • HD streaming
a realistic simple fall morning routine of a high school student
Confession #4,910
I think I'm starting to develop stress incontinence due to my dysautonomia (we think it's autoimmune and maybe even from CIDP and therefore progressive) and I have NO ONE I can tell I can't find a gynecologist to measure my pelvic floor strength before 3 months from now and I'm too embarrassed to tell my family or friends or to ask for help finding a doctor I'm only 24 and I don't want to lose another organ system to this disease, especially not one that is so stigmatized
Chronic inflammatory demyelinating polyneuropathy - Wikipedia