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Wow! I don't yave hearing loss yet, but I do have tinnitis (ringing in the ear)

primarily in my left ear. It's so bad that it hurts my ability to focus on

anything because it's so loud and I can't tune it out. There is nothing that can

be done for it through conventional medicine. Talking on the phone is difficult

as well as watching a movie or t.v. show. I had suspected it was related to the

implants, but now I'm convinced!

My only question is to Rogene...

How did you know that it was fungus related? it seems lots of things a fungus

related when it comes to implants! But how does one find out? Could my body be

totally infested with fungus right now and I don't even know?

Eeeeeewwwwww!

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A neurologist who spoke to the Fort Worth implant

support group commented that he was seeing an

unusually number of implant women coming to him with

hearing loss. . . He asked for a show of hands of

those whose hearing was affected.

An alarming number raised their hand. The woman next

to me said that her hearing (in one ear) turned off

suddenly while she was on the phone. It never

improved.

I was dx'd with Menier's disease - but I never

experienced vertigo . . . I insisted at the time I

didn't have Menier's - but finally gave up. A few

years ago an ear doctor agreed I didn't have it. I

would have had continuing bouts of vertigo with

progressive hearing loss if I had.

Rogene

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