← Return to Central Nervous System Vasculitis and dealing with brain fog
DiscussionCentral Nervous System Vasculitis and dealing with brain fog
Autoimmune Diseases | Last Active: Dec 14, 2023 | Replies (13)Comment receiving replies
Replies to "Hi @babsg1, welcome. I'm inviting @leezer and @vcornette1 and @SusanEllen66 into this discussion to share their..."
Hi Colleen. I had primary CNS vasculitis 11 years ago that attacked my brain. I was on chemo for approx 9-10 months. Fortunately I survived yet found myself struggling for words afterwords. I tried going back to work and did work for 7 years after the CNSV. Started out fulltime then to part time then gave up. I had difficulty focusing on tasks, unable to make decisions and carry through, brain fog and cognitive problems. I muddled through life and knew I was not the person cognitively that I used to be before CNSV. Then in Oct 2021 I was hospitalized with Covid. I was fortunate to leave the hospital alive. My daughters were very happy. Now I brain fog, chronic fatigue, insomnia, irritable moods, headaches, etc. Absolutely no motivation to exercise and I was previously a “gym rat.” After I stopped working I turned to exercise to feel better. Now nothing. Somewhere along the way since Covid I lost my motivation for life. I am not suicidal, It takes every once of energy I have to get thru a day.
Hope I answered your question.
Thanks, but I don’t have CNS Vasculitis. My Polyarthritis Nodosa has caused me to have peripheral neuropathy.
I have brain fog from fibromyalgia.