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Lyme disease Meniere's

Posted , 7 users are following.

patvj
patvj

I've just been diagnosed with Lyme disease.  I wonder if there is a connection with Meniere's Disease.  This has caused partial face paralysis.  Any suggestions?

0 likes, 17 replies

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  • patvj
    patvj

    Posted

    From the nuerologist wh treated me in emergency there are two. Nerves hat run clise to one another in the brain.  One somehow is related to Meniere's and the other Lyme's.  He said he didn't belueve that the Lyme's could be causing the Meinier symptons but still hoping

  • elizabeth48439
    elizabeth48439 patvj

    Posted

    Hello there!

    I know this post is old but i feel i must comment.

    I had tests in Germany as England don't test accurately for lyme....

    I show co infections for lyme and now I'm showing a weak positive on the nhs test for lyme he they still dismiss it!!!

    I am currently suffering recurrent sinusitis for 15 months now... i get dizzy and then today I've I've a horrible bout of vertigo come on! My left ear has tinnitus. I am wondering if i may have menieres. My dad has had ear problems over the yrars and he too has vertigo for past several weeks. My mother has had vertigo on and off all her life and doesnt know why and doctors didnt help. I know menieres can run in families ?

    Anyway not been back to my doctord yet as its constant battle with the nhs here and lyme. Argh!!! I had an elisa and 1 igg band positive me a me a exposure but i get told no you dont havelyme. I am sick of it and just want to get treatments. Currently seeing a herbalist! I have been left to rot with the labels ME andCFS and bIS over thepast 14 years and now ive got Pots too. P.ostural tachycardia sybdrome! Also can triggered by lyme hence i had the test.

    [b]I have removed reference to individual private clinics, which are not supported by UK doctors[b]

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