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Public Support Group 3,270 total results
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@hnickol, you're right that COVID-19 can make blood cells more likely to clump up and form...
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Well, I have counted over 100 symptoms, as most long COVID sufferers have. But originally, in...
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Daily, thanks for taking the time to respond with so much information. i have considered each...
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That blood type which I have among other other compromises like age, GCA, heart surgery in...
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Such an isolating sickness
I have posted before and read all of your posts, at least as many as I can. This month is 2 years I have been...
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Finally: Diagnosis. Oddly: symptoms have come in stages. Others?
A long post in hopes of learning of others who have had symptoms that were not initially experienced but came on in waves. After reading...
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Swaying feeling occasionally when I lay down nearly every night
So I had Covid in May this year and I had become extremely congested to the point I could barely hear and I also developed...
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Diagnosed a while ago with POTS but my BP...
I was diagnosed with POTS about 8 months ago when at my PCPs, I was dizzy and my face went numb. 180/120. A quick dose...
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Severe Allergy to Paxlovid
I am desperate and I can't find anyone out there that is talking about this. It has drastically altered my quality of life. If I...
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Living Alone: How would you prepare in case of getting COVID?
Recent reports are coming out that after initial recovery from covid, some are suddenly becoming very ill again with the virus. A recent article from...
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I'm very supportive, but she doesn't want it
I have read multiple people on the forum talk about a significant other not taking the reality of long Covid seriously. I have the exact...
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POTS, Pre- or Post-COVID: Where did you find treatment and what helps?
Hello- I’m looking for others diagnosed with POTS, whether you had it before or after COVID. I’d like to know if you’re willing to share:...
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