COVID vaccines and neuropathy
I am 85 with small fiber neuropathy that is getting worse. My neurologist thought it would be a good idea for me to wait with the covid vaccine and not be first in line to see how it affected other people with neuropathy. Probably because it is a new technology. Has anyone had a problem with neuropathy after receiving the vaccine? If so, which vaccine?
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I developed horrible nerve pain in my legs and all down my right side the morning after I was injected with the Senior High Dose Flu Vaccine! I had never in my life experienced this kind of pain. It has been over a year now with constant pain from my butt down my leg to shin and ankle. Doctor says this is impossible. One neurosurgeon out of several says it is possible. Do I take covid vaccine after this reaction that has ruined my life? Advice please. You don't need to agree.
My neuropathy increased a few weeks BEFORE I had my Pfizer vaccinations. Thank goodness it happened before rather than after, or I would have assumed a cause and effect relationship rather than just a coincidence as it obviously was in my case.
DO NOT PLAN ON ONE EITHER i HAVE NEVER BEEN THE SAME PAIN IN HANDS FEET KNEES EVEN ELBOWS BARB
I *think* I may be getting better.
I'm taking a shitton of supplements and anti-histamines and Gabapentin (up to 300 mg 3 times daily).
I eliminated B vitamins after reading that an overload of those can cause neuropathy type feelings.
I quit wearing compression socks because they were actually making the tingling in my calves worse. I have loosened all of the laces on my shoes because it seems that my feet and legs swell throughout the day and that makes everything worse.
Everything I'm currently taking (I KNOW it sounds outrageous, but I don't know which combination is working, so I'm afraid to eliminate anything):
- Gabapentin 300 mg 3 x daily
- Fish Oil with Vit. D (always have taken) 1200 mg/50 mcg 1 x daily
- Magnesium 100 mg 2 x daily
- Bromelain 600 mg 2 x daily
- Alpha Lipoic 1200 mg 2 x daily
- Montelukast 10 mg 1 x daily (always have taken)
- Sulindac 200 mg 2 x daily (acquired for previous injury & doctor refills for arthritis problems)
- Famotidine 20 mg 3 x daily
- Ceterizine 10 mg 2 x daily (afternoon and evening)
- Fexofenadine 24 hr 180 mg 1 x daily (morning)
- Glucosamine/Chondroitin/Tumeric 1500/150/150 2 x daily
- Probiotic 1 x daily
I drink 1 protein drink (Ensure Original) every morning with my breakfast of pills.
I also try to drink at least 1 Body Armour daily because I suck at drinking water.
I've been to a GP, Podiatrist, Acupuncturist, Chiropractor, Massage Therapist, and Physical Therapist.
My feet are just barely tingly at this point. My fingers still zap on occasion. My lower back sometimes feels like hell, but it's intermittent. My joints still ache, but they always have, it's just up a couple of notches. I still have that one weird hot spot on my right outer thigh (that was my very first weird symptom).
Can you believe that I'm still having sneezing and slightly runny nose from allergies with all those anti-histamines (off label doses) I'm taking? Unbelievable!
Said I'd report in... I'll continue to keep you posted. I wish everyone the rebound I seem to be experiencing.
Forgot to add...
Red Yeast Rice and CoQ10
I am also worried about getting the booster. I did have stiffness in my feet and muscle aches before vaccine they are worse now but never associated the two until i started reading this site. My neurologist said to get it but i am holding off for the booster a little bit and being extremely careful
I’m wondering if symptoms will improve as antibodies from vaccines wear off over time? How long has it been since your shot? I’m coming up on 6 months and feel like my symptoms may be improving as antibodies slowly regulate? I’m not taking anything except occasional CBD lotion on my feet at night, when the burning seems to be worse.
I'm 8 months out.
That's my hope too. If they're saying we need a 3rd dose due to waning, hopefully it'll just wane itself out of my body.
I have gone on every dies known to man. Nothing affects my neuropathy
Thank you for the kind words. I was lucky that my symptoms have lessened over time. I still get some slight numbness and mild tingling but at this point it's very tolerable. Time was my treatment. I hope that your son has relief soon. Take care.