← 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 Colleen. I had primary CNS vasculitis 11 years ago that attacked my brain. I was..."
Hi @babsg1 !
I’m another foggy one.
Reading your post made something clear to me about myself that I have not been able to put a name on yet. Motivation.
I have the same lack of motivation to exercise as you do and I used to be very active. Also, losing motivation for life. I’m not suicidal either, maybe a bit depressed, but mostly sad.
I have the feeling that my life is over- I’m 77.
Logically, I know I’m totally wrong. I have had therapy for a long time- I don’t think it helps anymore though.
My brain fog from fibromyalgia started when I was young -stress from work. Hereditary too.
The fog thickened after chemo for breast cancer 30 years ago.
13 years ago I was diagnosed with autoimmune colitis.
It waxed and waned for years- I didn’t function well for years.
I finally had immunosuppressive treatment 5 years ago, clearing all colitis symptoms.
I still had mental and physical fatigue, but tried to get back to normal activities.
Something strange had happened- I could not remember how to hit a tennis ball! I had played for years. I finally got the hang of it- but I don’t have the same edge.
Also, I had difficulty parking the car straight in a parking spot and judging how far in I was.
I’m still not “ normal “, I still have some inflammation in my GI system. Fatigue follows.
Sending you an energy hug!