Shingles Vaccine a trigger for symptoms of Meniere's?
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For years I rarely had a full blown Meniere's vertigo with uncontrollable vertigo, nausia, etc. About a month or two after I decided to take the shot for Shingles I woke up one morning with one that was so bad my husband had to take me to the ER. Since that time (for over 3 years now) I have had bouts sometimes as many as 8 a month with dizziness, full head feelings, that I can control using meclizine. I read in an article about Meniere's that some people think that Meniere's is related to or possibly caused by the virus that causes chicken pocks and shingles. The shot I had contained a live virus to give me an immunity to getting shingles so I'm wondering if it also caused a flare up of Meniere's. Has anyone else had this happen to them or do you know anything concerning a relationship between Meniere's and shingles vaccine?
0 likes, 35 replies
tim63896 patricia69095
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Hi there. Sorry to read about your symptoms. Regarding a viral cause for menieres, I take an antiviral, Aciclovir. I started on a high dose and then reduced after a few months to a maintenance dose. Since I have been taking it, for some years now, I have never had another attack. Worth reading up on the research of Dr Richard Gacek who has trialled and uses antivirals to treat the symptoms of Menieres. There are many ent's ,particularly in the uk, who dispute its validity but none of them can point to any research to support their view.
patricia69095 tim63896
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I appreciate your reply. When I asked my present doctor about the possibility that the vaccine for shingles had exacerbated the minere's symptoms, he told me that it wasn't possible. I wonder if he's since seen this doctor's work?
jackie72283 tim63896
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bonnie_97384 patricia69095
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I personally don't trust the Doctors regarding our diagnosis. I strongly believe the Shingles Vaccine I got caused my illness and they are protecting the pharmaceutical companies
dee5400 tim63896
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jenn34106 tim63896
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do you still maintain a low sodium diet?
JMJ patricia69095
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Hi Patricia,
I know that there is at least one forum member who has had great success with the Richard Gacek protocol for MD — I'm pretty sure he still takes a maintenance dose of Valtrex, daily. I wish I could remember his name, but I can't. And I have searched the different threads, and I just can't find the one where we had this discussion. I hope he'll see your question and eventually respond.
I went on Gacek's protocol shortly after I was diagnosed, but I did not experience any improvement. However, his study makes a lot of sense to me. And, I can see why you'd make the connection, having just had the Shingles vaccine a month before your symptoms "blossomed."
I don't know what the underlying cause of my MD really is, but the episodes of vertigo were very severe and very frequent. I have had to go on intratympanic injections of steroids in order to control the vertigo.
I'll bet if you wait a bit, someone will notice your post, and be able to share more about their experience.
If you haven't read the Richard Gacek studies, it would probably be very helpful. I made copies and brought them to my ENT, which is how I managed to get on the anti-viral protocol for MD, early on.
I'm so sorry that you're having such a rough time. It's a terrible disease. I wish you all the best.
Sincerely,
J
patricia69095 JMJ
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JMJ patricia69095
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Yes. And, there are many additional articles out there about his work, as well.
Wishing you all all the best,
J-
angela84522 patricia69095
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Hi there. I had Shingles last Dec 25 and lasted a couple of months. My Vertigo and all other issues with my MD doubled and trippled. Yes I think your on to something. I have too researched into it. Of coarse mine wasn't the vaccine it was just getting Shingles.
patricia69095 angela84522
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angela84522 patricia69095
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JMJ angela84522
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Hi Angela,
I can't imagine a worse combination than having Shingles along WITH vertigo!!! Arrrrgh! You poor thing!
I had Shingles about 2 years before my MD, so I have no idea if one resulted from the other. However, when I read Gacek's studies, I found them to be convincing.... and it's a very low-risk protocol. I wished the Acyclovir and the Lysine worked for me, but neither thing did the trick. I'm so happy to hear that the lysine helps you!! I say, if it works, keep doing it! 😀
Take good care,
J-
patricia69095 JMJ
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I talked to my doctor about taking an antiviral medication and he gave me a prescription for Acyclovir 800mg 4 times a day for 7 days. He figured it couldn't hurt I guess to humor me. He was familar with Gacek but didn't know about his use of antiviral meds for MD. Do you happen to know what dosage and frequency Gacek recommended? I took one pill this morning and ended up with a lump in my throat and tingling around my mouth...side effects? I'm afraid to take more. I took it with a banana and didn't experience any nausia (which is a more common side effect.) Now I'm not sure what to do.
JMJ patricia69095
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Hi Patricia,
I took Valacyclovir, 1 Gram 3 times a day for 30 days. The plan, as I recall, was to reduce to a maintenance dose of 1 Gram per day, but I was still getting so sick that my ENT abandoned the protocol and referred me out to an Otolaryngologist who treated me with intratympanic steroid injections.
I didn't experience any side effects at all, with the Valacyclovir. But they didn't help, either. I know however, that they have helped a significant number of people.
As with any other drug, if you suspect that you might be having an adverse reaction to the drug, then it's always safest to simply stop the drug and call your doctor.
I'm so sorry that you're having such a hard time. I really do know what it's like to be willing to try anything in order to feel better! It's so frustrating because it's really impossible at this point for anyone to identify the cause of MD in all people. We just don't know. What they do know is that MD is typically progressive. Some people go huge gaps of time without any symptoms, and then out of nowhere, the symptoms come back and really incapacitate them. With others, it's more of a chronic thing, that never goes away, but gradually increases in intensity...There seems to be no single pattern to the progression.
Just don't lose hope! If you can't take the Valcyclovir because of a bad reaction to the pills, there are still other options for you to explore.
I wish you the very best. I hope you can find an answer and feel much better, soon!
Take good care,
J-
patricia69095 JMJ
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bonnie_97384 angela84522
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bonnie_97384 JMJ
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