Newcomer to the Forum but Not Tinnitus

[glynis]

Hi,
My name is glynis and I have severe Bilateral tinnitus due to having Bilateral Menieres for ten years and over .
I am well up on tinnitus and Menieres and been on the BTA forum since 2011 giving good advice and take calls and emails and texts.
I also run a tinnitus support group with Dot at dDeaflinks in Shelton.
Happy to be here and help members also having problems with tinnitus and the unwanted emotions it can cause and help with Menieres Disease also...lol glynis

 

[Markku]

Hi,
My name is glynis and I have severe Bilateral tinnitus due to having Bilateral Menieres for ten years and over .
I am well up on tinnitus and Menieres and been on the BTA forum since 2011 giving good advice and take calls and emails and texts.
I also run a tinnitus support group with Dot at dDeaflinks in Shelton.
Happy to be here and help members also having problems with tinnitus and the unwanted emotions it can cause and help with Menieres Disease also...lol glynis

Welcome Glynis!

I know @AnnaW is our resident Meniere's expert, also from the UK I believe. You two will come along great

You seem to have extensive history helping and supporting people with tinnitus, you are an excellent addition to our little forum!

If you have any questions re: how to use the site or anything like that, you can always send me a private conversation.

Have a great rest of the weekend,
Markku

 

[glynis]

Thank you Markku for a warm welcome and glad to be on board helping other Members...lol glynis

 

[billie48]

Welcome glynis. We surely welcome someone as experienced and helpful as you to come help lift up the spirit of some desperate new sufferer. We love to have you sharing your experience and insights to the struggling members. Hope you will find in TT a supportive and friendly atmosphere.

 

[AnnaW]

Hi Glynis,
Nice to meet you. Sounds like you do some great things to help the menieres and tinnitus community. I too have bilateral menieres and tinnitus, I have been unilateral for 17 yrs but went bilateral 2 yrs ago. How does menieres affect you?
Anna.

 

[Richard zurowski]

Hi Glynis your help would be most welcome.and welcome to the forum.

 

[Mike TerMaaten]

Hi Glynis. Glad to hear your story. Glad to have you here

 

[Karen]

Welcome, Glynis! You are a positive, supportive voice that is very much welcome here at Tinnitus Talk. We're very glad you've joined us!

 

[Gena94]

Hi @glynis another memeber gave me your contact info because I think I might have meniers disease as well.. I started getting this vertigo feeling not too long ago and it came on so sudden I barley noticed it. Until I began sitting down and feeling it, laying down and feeling it. The only time I don't really notice it is when I'm standing. Idk what else this could be and it's so hard having no one to talk to about this.. could I text or email you?

 

[glynis]

Yes thats fine ....just getting up but will reply to you asap ....lots of love glynis

 

[billie48]

Idk what else this could be

Vertigo can be caused by a few causes, Meniere's being one of it. If that is proven the case. Glynis is your best source of information here. If it is due to BPPV, like what I once had, it is easier to fix. Simply follow this exercise created by this lady MD and it will help. I did the exercise once or twice and my vertigo was gone and never come back. Good luck. Take care. God bless.