I can not begin to tell you how sorry I am that you are going through this, all of us actually. Until I found this site and my LC doctor connected me to another LC support group (via zoom) I thought it was an anxiety disorder like sooo many doctors tried to tell me. Honestly I think I would have rather them say “ Mrs. Bryant we just can’t figure out what is wrong” instead of making me feel like it’s all in my head. Two years I spent in and out of hospitals and doctors offices, it wasn’t until a family member said I should look into Long Covid, and she’s heard several stories of people experiencing what I was. For two years not one single doctor suggested that Covid could be the root.
We are all so lost and hanging on by threads most of us, I can’t even remember what it feels like to NOT have symptoms, to feel like my pre Covid self. I don’t cry as much as I use too, I guess it’s just me accepting this is it…for now. But I also had to face I might be like this for a long time. I want so much for that not to be true.
I send out to you and everyone on here healing energy, prayers for better health, and days where all of this will be nothing more than a memory and we make it to the other side of a full recovery. ❤️