2Cor.12:19
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Your description (to me) sounds like you developed POTS from the vaccine which is actually more common than people realize. The fact that it affected your ability to stand and that you are now on a beta blocker 21 years later, sounds like POTS (not panic disorder). Have you ever been diagnosed with POTS?
@Gingergrrl, My inability to stand up was temporary and accompanied the severe panic attacks. The beta blockers were given for an arrhythmia and to help control the panic attacks- along with XANAX, which I’ve finally begun to wean off - ever so slowly, after 20 + years. . The leg weakness I had then was nothing like POTS. I do have POTS now, but it came on many years after that. Was dx’d by my cardiologist who tried beta blocker regimines, compression socks, increased water, salt, etc. Fortunately, mine’s not as bad as some have it and it tends to come and go. I use a cane for my balance problems due to Axonal Polyneuropathy so it comes in handy if my legs get weak.
I can sure see why you don’t want to risk the vaccine. Holding a good thought for you friend and that you’ll stay safe and COVID will disappear.
PS. I should add that when I had the vax reaction, I had yet to be treated for Hashimotos ( which Im sure I’ve had since high school as I was on T meds back then but stopped taking them. That was before they tested for Hashi’s) I also had yet to be diagnosed mixed sleep apnea which I developed when I first got sick with ME/CFS. So both of those conditions can cause anxiety and panic episodes. Once they were successfully treated, my panic attacks improved dramatically. That could have played into the whole vax reaction.
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