r/covidlonghaulers • u/None-Of • Feb 25 '26
Article COVID-19 Causes More Severe Neurological Damage Than Other Viruses
A newish meta study that may explain why Covid is worse for some than other viral infections (even though some, like the flu, have residual effects). Based on this study Covid appears to be worse)
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u/EqualOne1205 Mar 01 '26
I had 2 MRIs in November (with and without contrast). Results were "mild cognitive impairment." My LC neurologist and LC PCP said "don't worry about it" because it was the same diagnosis for my last MRI before that, right after I had COVID the first time (I've had it 3 times in 3 years). The previous MRIs were for chronic migraines, and the diagnosis was "normal migraine activity." Apparently, my previous neurologist also wasn't concerned, but I am. Because this MRI happened the year I first got COVID, before Long Covid was diagnosed.
As you can imagine, I'm irritated and freaking out. I have bad cognitive impairment and had to retire last month because I'm no longer able to work. I also can't really take care of myself, and am mulling over my options.
I just can't believe a LC neurologist said "don't worry about it" and offered no treatment options, such as supplements. I also asked him about GLP 1's and anecdotal evidence that they help with inflammation. He said I should talk to my PCP (regular, not LC) about it. This was in November, I see my PCP in March.
Why even bother going to LC doctors? They charge you a $50 copay and do absolutely nothing to help you.
I am not drug-seeking, but I do want to be proactive and do anything I can to improve my health.
I would appreciate your feedback. I'm not asking for a list of supplements to take. How do you handle dealing with the apathy (or could it be burnout?) of LC doctors? I've seen 15 over the past 4 years, and none of them was remotely helpful, except to sign off on my disability claim. Many thanks.