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COVID vaccines and neuropathy

Neuropathy | Last Active: Nov 7 12:50pm | Replies (2237)

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@avmcbellar

Hi @jimhd nice to hear from you. I would give another stimulator a chance first before trying the pump. What is your reasoning for the pump, ease? Keep in mind no matter how many times you press the button for medication you will never get more than the amount prescribed. As for the vaccine, the side effects are scary. I don’t think the doctors have a handle on it because they just repeat what was said to them( mostly by the vaccine manufacturers). We are all different when it comes to medical history. We look at what we can tolerate to make our decision. Wish you the best. Toni

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Replies to "Hi @jimhd nice to hear from you. I would give another stimulator a chance first before..."

@avmcbellar There are a couple of reasons for considering a pump, the primary one being replacing oral medications with more effective intrathecal delivery. The research I've done has indicated that the pump requires as little as 10% of the oral dose. Of course, there's not a lot of certainty in any medical treatment, as no two people are the same. My neurologist mentioned to me this morning to ask about the possibility of a bolus delivery option to treat breakthrough pain. I understand that once the therapeutic dosage is determined, it works automatically, and is a safer treatment in terms of abuse or overdose.

My wife and I are scheduled to get the vaccine on the 30th. I'm more than a little concerned about the impact it might have on my neuropathy. I don't know which one is being offered here, and I need to schedule an appointment for the 2nd shot.

I've never had any reaction to vaccines until the 2nd shingles vaccine a month ago. The injection site is still sore if I lie on my left side, though I didn't have any immediate reaction. I'm hopeful that the covid vaccine will be effective but benign.

You wrote in the past about eye exercises. I asked my neurologist about that, as well, and he put in his notes to consider it, whenever I'm ready. Prisms corrected the double vision for a month or so, but it returned, and sometimes I see 3 images. When I asked the ophthalmologist what else can be done, he said get used to it. Not a very helpful response. Perhaps you could recommend some research on the subject. Preferably in layman's language.

Jim