Sep 20, 2021
Had to share! Found this in 'Fibromyalgia memes' on facebook
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Had to share! Found this in 'Fibromyalgia memes' on facebook
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
Yeah, I hate waking up and not knowing if I’ll be able to walk around, or if I won’t be able to stand for more than a few seconds, or if I will be able to walk myself to the bathroom. But what I hate the most is when it takes a few moments to fully wake up and process everything, and when you do the first thing is: pain.
Been trying to figure out how to start talking abouty new diagnosis of Fibromyalgia. It's an answer. It brings new meds, new therapy...OT and new PT, and pain management.
It brings a name and new research to focus on. I'm trying to allow myself to be hopeful even though I've been exhausted by this process that's stretched into years. So that's that. Still standing (sometimes) still walking forward. Still doing my best to manage my body and leave my mark on the world.
My day in a meme
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
Post-diagnosis depression is so annoying like
I have the thing,
I know i have the thing,
I have been telling my doctors i have the thing
I’ve known I have the thing for the last five years
I’ve basically been treated for the thing for the past three years
I’ve been through the diagnostic tests for the thing knowing i have it
But being told i have the thing leaves me depressed and bed ridden for days😅
⚠️REPORT⚠️REPORT⚠️
From Tiffieanna herself
- I’ve been experiencing a chronic migraine for over three years now and have started Botox injections for such. It has been difficult I’ve only just began and the pain is incredibly unbearable.
- & before the Botox session began I start having full body spasms, having such with my fibromyalgia and my mild scoliosis and sciatica it was definitely not pleasant in the sliest. I was finally able to talk to my doctor about it and she said it sounds like Soto syndrome which also doesn’t sound right, hence we’re still looking into it.
- So while I’m taking Botox I’m seeing my neurologist over my full body spasms/Soto syndrome. Of which has all been crazy scary.
- Thought I’d give you all an up date ( ﾉ₃ இ ) ❀
You know you're an empathetic spoonie when you're glad you're home alone so no one can see the pained faces that you make