New, but new to Menieres.

Hi Bella,
Welcome to the forums. Sorry you have this awful disease. The boards have alot of information that might help you get relief from your symptoms.

 

Hi Bella.

I think I might be able to direct some doctors or resources pages you can look up.
http://www.menieres.org.uk/files/pdfs/balance-retraining-2012.pdf - this is balance movement exercise.
http://www.menieresdiseasestudy.com/78.htm - Meniere's Clinical Trial
http://menieresexperts.com/ - Meniere's Doctor website

These might help you!

 

Antivirals help me tremendously, I haven't had a vertigo attack in the last year and 6 months while taking acyclovir and I have MM for 48 years.

 

I meant no vertigo for 1 year and 6 months

 

I just joined this forum. I have read several comments and I think I am in the right place! I was diagnosed with Meniere's in April of this year after an eight hour episode that landed me in the emergency room. I was glad for the ER visit because that time was used to eliminate other possibilities. When I went to the ENT a week later they had all they needed to help rule out any other disease. I am looking forward to reading more about everyone's experience. I can identify with some of what I have read so far. Before I start asking questions I am going to look over the topics and see if I can get some answers from what you have already discussed. Glad to be hear and looking forward to meeting some new friends.

 

Somehow I mis-filed raymonds story (ha under VA medical), a couple of years ago.

Glad I found it and this web site again. Looking forward to
reading and sharing.

coping with my own private "funhouse" in Ormond beach. Still play golf
(ha ! great excuse for bad shots), ride bike (not on raods anymore), ease meniers fun filled
events with meclizine.

looking forward to sharing with my peers

Bill