Shingrix and peripheral neuropathy
4 days after my 2nd Shingrix vaccination, I suddenly developed intense peripheral neuropathy in both feet...for the first time in my life...anyone else?
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I also, had my shots in 2019. Same thing with me, feet, burning throughout body, affected legs, etc. Had every test done under the sun including neurologist testing and nothing was found. As fast as it came on it lasted 4 months then disappeared, now the burning and numbness started again in the feet only when I sleep. Who knows what these vaccines can do, and if things can be recurring. I had to have therapy on my legs because of the vaccine as I had no balance, could hardly walk, etc.
My husband is a two time stem cell transplant patient, he was told at Mayo not to get the shingles vaccine. His current oncologist has not reversed that recommendation with the newer vaccine.
@auntieoakley First, I meant to ask if anyone else had been told to not get the shingrix vaccine.
Why was your husband told to not get Shingrix since it is not live? Is he by chance also a patient at Mass General? They are waiting for approval from the infectious disease department. Granted, I am sure that department was over-burdened the last year and a half but this has been going on since well before the pandemic.
JK
It was my understanding that because it was a live virus, and he has had two stem cell transplants that it was a risky business. Then when they came out with shingrix some time later. Our current doctor said let’s wait and see. It could be because it is so new and my husband is off and on treatment for multiple myeloma, and he is somewhat fragile health wise. We haven’t revived that conversation since then. Our doctor is a proponent of vaccination. He revaccinated my husband with all the childhood vaccines after transplant.
Is Mass general holding it up for everyone or just certain groups of patients. Truth is I haven’t had it either, and since I have moderate peripheral neuropathy this thread is making me question the wisdom of getting it. I had shingles in 2019 and was told to get it after 6 months but then we were in a pandemic and then I got the COVID vaccine and they said wait at least 4 months which would be July.
@auntieoakley Sorry, I thought you meant he had been told to not get the Shingrix vaccine. I know that the prior one did have live virus in it so was not recommended for anyone with a compromised immune system. I did have that one when I was pre-transplant. I don't know how long it lasts though, it was quite a while ago.
I only know that the transplant department is not advising it for post-transplant patients. The ruling is determined by the infectious disease department but I don't know if other areas are also affected.
After seeing what my sister-in-law has gone through, and is still going through to some extent, I want to be protected. If your doctor says with your peripheral neuropathy it's OK to get it, I would get it. My husband had a post-retirement job where many other retired people were employed and he knew a couple of people who were out for months with shingles.
JK
Thanks for that. I am usually first in line for any recommended vaccine. I am sure if my doctor says get it, I will. That being said I am going to ask one more time relating to this thread before I do that.
I realize your post was from back in 2019. Wondering how your symptoms are now. I got a Shingrix vaccine, with the 2nd dose in Feb 2021 and have had similar symptoms to what you describe and more: burning, tingling, prickly, scratchy sensations in back, near elbows, above needs, calves, feet for 5 months now. Had thoracic MRI done - normal. Blood work for all kinds of things all came back normal. Getting an EMG done here soon. I took an antiviral med for 3 weeks (probably about 5 months too late) and now Gabapentin for the past month. All regular clothes feel like sandpaper on my back so the only clothes I can wear are anything made out of nylon. Can't sleep on cotton sheets, too scratchy. At least I can wear some clothes. Like you, hoping this doesn't last for life. There can be worse things, but aggravating when you try to do something good for your health and it turns out bad. If I would have known what negative things Shingrix could do, I would never have gotten the vaccine. Not all vaccines are good for people and anything we do, whether we get it or not, has risks. I have good days and bad days.
Hello @addy60 -- Welcome to Connect. @19jimmy57 did give an update that his symptoms were not due to the Shingrix vaccine in a later post here - https://connect.mayoclinic.org/comment/243864/
I had both Shingrix vaccinations a few months ago but only had a little fatigue and a sore arm from both. I'm sorry to hear your experience was not good. I think each of us has to weigh associated risks. I have known folks that had shingles and it's very painful and I definitely do not want to experience shingles.
You mentioned you will be having a nerve conduction test soon. Can you provide an update after your appointment?
Thanks for pointing me to the updated post by 19jimmy57. Yes, will give an update on the nerve test later.
when I first was diagnosed with neuropathy blood tests showed that I had a very high level of B6 (246) in my system. After I quit taking all supplements that content B6 my level came down to 35 however my non-diabetic neuropathy is getting worse. My Neurologist told me a year ago that it would take about 6 month to show some improvement. Just the opposite. I am watching my diet and drink lots of water. My lower legs are numb and pain full and swollen around the ankle. Makes i hard to sleep.