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've had PN for years now. I have the numbness and tingling but zero pain. I had Covid when it first came out and I had the Moderna vaccine. I’ve been taking the Moderna boosters ever since and it’s been over two years since I had Covid. I have zero pain and never had any pain. I have balance issues but I still walk without a cain. I’m a 85 year old male.
Moderna had a negative effect x2 on my PN. I’m 62 and won’t do another Covid shot.
No I am not diabetic
I am 72 and was diagnosed with CIDP after my third Pfizer COVID-19 vaccine. There is very little information on the link between CIDP and the COVID-19 vaccine but I'm inclined to think they are related, I've had iViG and heavy doses of methylprednisone(steroids) and neither have helped. I am getting weaker and easily fatigued. Does anyone know of any other treatments that might help me? I am looking at VyVgart Hytrulo as a possibility, but it is $17,00 per dose.
Thank you,
John
So Sorry. What is CIPD? I never heard of it.
Best of luck to you. Think positive. Something will help eventually.
Chronic Inflammatory Demyelinating Polyneuropathy,
Thanks for the thought
Steroid 150 mg IV
Every 4 hours
2 Benadryl one hour prior to infusion
Tylenol 500 mgs
Wait 30 minutes and I am on Panzyga IVIG
Just an fyi I was told to drink 100 ounces of water day before and 100 ounces the day after to prevent migraines after infusion
WOW!!!!! You sure are going through so much.
Best of luck to you.
How much IVIG? Mine is 5 days a month. It has gotten rid of my dizziness and balance problems. My left leg was dragging along with drop foot. My left leg is not dragging any more. I am waiting to see how long it takes to work on the motor neuropathy. I have several types of neuropathy plus mine in autoimmune related.
I was getting IVIG on two consecutive days every 4 weeks. After 5 months of no improvement it was discontinues. I was referred to a specialist at Penn Medicine and an now on high infusions of methyl prednisone which don’t seem to be helping either.