Is there any way to treat brain fog from autoimmune illness?
did anyone tried vortioxetine for the treatment of brain fog from autoimmune illness? if so did it benefit you in some way? thanks.
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i wonder then are you able to sustain a job and function with this conditoin?
Sorry for the delayed response.
Yes - I got through grad school and did research work for a few years before I knew what was causing my symptoms. I was pretty miserable but economic survival is a strong incentive.
After learning that I could control my symptoms with avoidance I tried to work and live in environments where I was not sick all the time.
I was reasonably comfortable and productive in an off-campus university lab that was built to my specifications but was only there for 5 years. My productivity and comfort decreased significantly after I moved into an on-campus that was designed by university architects.
After leaving the university I did consulting work and small scale product development in my home or in spaces that were 'built out' to my specifications.
I am currently retired and am able to practice avoidance at a level that was not possible when I was working.
Please test each space you plan to be in before signing a lease or purchasing! I have MCS and also had a mold exposure which created a two year infection in my sinuses- this had to be treat with spraying an antibiotic with a syringe to get to the infection.
If you can find a place that has a moist heat sauna this will help you sweat out the sensitivity .
I put in hard air ducts where I have lived for the past 25 years, and have them cleaned every two years. This really helps.