Health problems from COVID injections increasing your immunity.

Not neuropathy, but POTS after a Covid booster.
Postural Orthostatic Tachycardia syndrome.

I already had ET, Essential Thrombocytosis, a chronic leukemia from long covid…

@caban, have you been diagnosed with autonomic neuropathy? Or perhaps a immune-mediated neuropathy?

Here's some information that may help:
- Immune-Mediated Neuropathies: Pathophysiology and Management https://pmc.ncbi.nlm.nih.gov/articles/PMC10139406/
- Autonomic neuropathy https://www.mayoclinic.org/diseases-conditions/autonomic-neuropathy/symptoms-causes/syc-20369829

Not neuropathy. I developed coronary microvascular endothelial dysfunction (a heart condition) within 2 weeks after my first Covid vaccine. From what I've read, both the vaccine and Covid itself can cause the long-lasting symptoms that are grouped together and described as "Long Covid" or "Post-Covid Condition." Neuropathy is one of those symptoms . . .

Once I googled low glutathione levels and endothelial cells and it said: Low levels of glutathione can impair endothelial cell function. Worth doing some research. But always consult your doctor before adding any supplement to your diet.

My neurologist is giving me a test for neuropathy at the end of the month.

Hello
Yes heart problems are often talked about as a result of Covid injections. Neuropathy is another one. Doctors know about it but are very careful about what they say to you understandably … from my personal experience. It’s a shame that this happens as so many people must be told their neuropathy is idiopathic when it could have a possible cause such as the one mentioned above.

Now I wonder if my POTS was from a covid booster.

I went from very early COVID to ET, a chronic leukemia, then POTS.
POTS was misdiagnosed as long COVID for 2 years, but that doesn’t matter because none of the meds help…

@janetbender POTS is often part of Long Covid. Which meds don't work - POTS meds or Long Covid meds?

POTS - I had bad reactions to Midrodine and Fludrocortisone.
I tried each separately and then both together.
I wear compression knee socks, drink electrolytes, use protein powder,

I also went to an Integrative Medical Doctor who revommended:
no bread / flour / sugar, no fried food, no oatmeal, cook most food from scratch, eat protein 3x daily.
vitamins added are Alpha lipoic acid and CoQ10. She added more vitamins but I can’t take any more!

I see a physical therapist who specializes in Long Covid, and one of the things she works on most is POTS/orthostatic intolerance. She's helped me a lot. She started me on exercises to strengthen the area between my neck and my knees, the place where the blood pools (when it's supposed to be pumped to my brain . . . ).

You can search YouTube for videos about exercises for POTS and find pretty much everything she's had me doing. I like working with a PT because it keeps me accountable, but doing the exercises yourself would probably still help.

I wonder if Long Covid meds might also help your POTS.