Me & My Tinnitus

My tinnitis started in early 2000 although I didn't have a name for it beyond "ringing in my ears". By spring, I had my first and worst Meniere's attack......vertigo and related sickness lasted for nearly 14 hours. For several years, tinnitis and Menieres attacks came together and all was "silence" between attacks. In more recent years, tinnitis became an every-day occurance; the volume got louder louder just before an attack. Just this autumn and early winter, Menieres attacks are coming 3X/week on average; tinnitis has become unbearable. Otherwise, in my life beyond Menieres, I am mother to Amy, grandmother to Tony and Tori, partner to Larry, retired and living by the sea. I love reading, films, sewing, quilting, paper arts.

 

Hi Karen. thanks for the welcome. My ENT has not offered treatments except for liw sodium diet and diuretics which made me dizzy. Also have progressively worsening hearing loss and got hearing aides last summer. Iniatially the hearing aides helped but not in the last 4 or 5 weeks. i am looking for recommendations on a natural diurectic.

 

Hi Pat and welcome...

I know little about Menieres, other than what it is. Have you looked for a doc who is an expert in this field? Low sodium and diuretics is basic treatment but I think there may be more options.

 

Thanks, LadyDi. i have been giving this idea serious thought. thinking about Massachusetts Eye And Ear in Boston.

 

Actually, if anyone has experience at MA Eye and Ear, i would appreciate hearing about it

 

If you are in the New England area, several good facilities and universities there. My experience had been: go somewhere where they are doing research, not just a large ENT practice. Makes all the difference. Hopefully someone here will know about MA Eye and Ear.

 

These folks, who are in Connecticut, are speaking at the Tinnitus Research Initiative conference in New Zealand in March, which says something. Major gathering tinnitus medical professionals

Www.hearingbalance.com

 

Thank you, Lady Di, for good information. Much appreciated! I just visited the CT website. Had no idea such an organization existed. Tinnitis makes one feel so alone; it is helpful to know TT is here and also such resources as the New England Center.