So, I’m not the only one who has shaky legs when I am brushing my teeth etc. Thank you for mentioning that! I told my doctors and they look at my like I’m crazy.
I share fibromyalgia, polyneuropathy, and other autoimmune diseases with some of you. These “annoyances” have really turned my life upside down and made me pretty much housebound.
I just turned 74 this week. Fibromyalgia has been with me for about 40 years at least. The worst of everything started after I had the flu in March 2015. My immune system went haywire, overreacting to the virus and started attacking me. December of 2015, I was diagnosed with Cutaneous Polyarteritis Nodosa. It’s a form of Vasculitis. It inflamed my arteries and that in turn damaged my small fiber nerves giving me neuropathy.
Things have continued to get progressively worse. Now I have polyneuropathy, Raynaud’s disease, kidney disease, and occipital neuralgia.
My vision has become blurry, and I’m seeing double in most directions. The ophthalmologist has said I need to wait and see, meanwhile my balance is off and driving is off the table.
Fibromyalgia causes extreme fatigue. I’m tired of being tired. I asked my neurologist if he could do a sleep study for me because I wanted to make sure I didn’t have sleep apnea. I did the overnight sleep study and it showed that I have idiopathic hypersomnia. Huh? Turns out it is also referred to as Narcolepsy 2. My brain doesn’t go into a deep sleep at night like it should. Therefore, I am never rested. I’m the walking dead during the day…
Sorry for the “book” I can relate to so much you guys have written. Only one thing, I can’t tolerate any of the pain medicines, so I stick with Tylenol.
This sounds VERY similar to the symptoms I experience. I have been diagnosed with fibromyalgia, central sensitization syndrome, Raynaud’s syndrome. I have suspected Vasculitis also but no doctor seems to help me locally. I’m curious how you received your Cutaneous Polyarteritis Nodosa diagnosis? Was it from Mayo Clinic?
Thank you in advanced!