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Depakote (valproate, valproic acid, Epival)

Discussion in 'Your Front Porch' started by AnneT, Jan 28, 2019.

  1. AnneT

    AnneT Well-Known Member

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    Anyone try this? My otoneurologist recommended it, a few years ago, for my lovely mix of migraine and MM, especially if I were to develop sudden onset attacks.

    Well, I'm here. I was doing well on Valtex and JOH for about a month, and now I've had 3 attacks in 3 days. This morning's adventure has got me really rattled - happened while I was driving. (I think I'm going to stop driving for now... or at least only on days I feel really good.) It's going to be 2-7 months to get back into my local otoneuro (even with crying on the phone to the receptionist). I'm awaiting results to send to the House Clinic - hoping they can see me faster, but who knows how long it will take for these results to arrive.

    Sorry, I'm rambling. My point is, I know Epival/Depakote may have lots of side effects, but I'm hoping it'll be a short term thing until I get gentamycin or laby or whatever. (Vive le laby!!) Epival may also help my mood and anxiety, and any migraine component. Just lots of shitty potential side effects.

    So, anyone on Epival/Depakote? Any experience you want to share, especially on its effects on MM vertigo, migraine, mood, driving?
    Please & Thanks
     
  2. AnneT

    AnneT Well-Known Member

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    Whoops - I meant to put this in the health thread - I'll copy it over there. Sorry for redundance.
     
  3. Marta

    Marta Active Member

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    Anne I am so sorry you are suffering so much. Have you read the thread about vitamin B5 and B 6? Perhaps it’s worth trying. I am going to take them for my tinnitus.
    Some people are lucky to get relief with supplements, vitamins etc , some need surgery. I hope your doctor is going to find the best solution for you!
    Stay strong Anne!
    Hugs
     
  4. AnneT

    AnneT Well-Known Member

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    Hi Marta
    Yup I’m trying the b vitamins for 2 weeks and diamox this last week- on top of the valtrex and assorted supplements. I also have less stress, and the weather has been more stable. I’ve had fewer vertigo attacks for about 3 weeks, so it’s hard to attribute that to any one thing.

    I’ll see a local specialist May 1. I’m hoping for gentamicin or laby; I’m also terrified of the vestibular recovery process. But I’m not driving because of drop attacks, so it’s time for definitive measures.

    My mood and anxiety are surprisingly ok the last few weeks too.

    Hope alls good with you
     
  5. Marta

    Marta Active Member

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    Anne
    I am so sorry to hear you are suffering. I will keep my fingers crossed for you on 1May. I know that one day you are going to get your life back and then... we might meet over clotted cream ice cream in London
    I don’t think you should be afraid of the vestibular recovery process. I know that is takes time but if you move around and do what you are told you will be more than fine.
    I did VT myself and it was so so effective! I did not believe it could change anything but it did! I keep my fingers crossed for you lovely lady!!
     
  6. AnneT

    AnneT Well-Known Member

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    Hi again Marta! Thanks for the encouragement.

    I’m trying to do my daily walking and random bits of yoga and tai chi each day. I see some VT online. I wonder about starting that in anticipation of a procedure? I’m kind of wobbly from the effects of my Menieres. But I’m scared of triggering vertigo attacks.
     

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