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What can I expect with Antiphospholipid Syndrome (APS)?
Autoimmune Diseases | Last Active: May 16 11:41am | Replies (188)Comment receiving replies
@wig,
P.S. Do you have tinnitus, too? I do and that is also connected to Ménière’s disease. Also, did you get the Covid vaccine and infection? I did and had bad reactions to the vaccine (pain at base of skull/lightheaded on days getting the vaccines), and new chest pain and breathing problems ~1-2 weeks after my 2nd dose of the vaccine. I thought I was having heart attacks (had 4 bad episodes in the morning over 4 months and had to ask my teenage son to hurry up and get me aspirin (couldn’t really yell for help it was that bad of pain). My understanding is the COVID vaccine and infection causes blood clots and endothelial/microvascular damage but isn’t talked about much due to politics and forced vaccinations to keep jobs. It has caused many to get more sick than they were pre-COVID vaccine. I know I got much worse after having both vaccine and illness in 2021.
Replies to "@wig, P.S. Do you have tinnitus, too? I do and that is also connected to Ménière’s..."
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Yes, I do have tinnitus. A low roaring - like the engine of an airplane. I think it's because I have reverse slope hearing loss. Most people with loss in high frequencies is a ringing. I don't understand fully but it's something to do with the brain trying to mimic the sound it no longer receives. I lost my hearing before covid and am lucky I had no lasting effects from either the infection or vaccines. Although I've stopped having them. I know people who've had terrible effects from covid. A friend developed seizures, someone else rheumatoid arthritis and his wife, atrial fibrillation. But who knows if covid was really responsible of not. Let me know what your brain MRI shows up. Thanks for your kind words and take care of yourself.