Physical activity and meniere symtoms
I have been told that increasing your physical activity should lessen the symptoms related to menieres. Although, i …
Meniere's disease (or syndrome, since its cause is unknown) was first described by French physician Prosper Meniere in 1861. It is a balance disorder of the inn...

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fluctuating hearing loss
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For so many years I thought I was loosing my mind. That everyone else was right. That I had to be having "selective hearing". In the last 2 yrs. since seeing Dr. Jeff Brown in Portland Oregon I have come to understand that fluctuating hearing loss during various levels of vertigo/menieres episodes is quite normal. When it happens though I understand it and have learned to live through it it makes me want to cry. I don't know anyone who understand this and so very often the sounds and words just blen together like meaningless noise and then bamm the 'filters' for lack of a better word shift and certain sounds/words are easier to understand again. I suppose this is a big cause of my depression too.
Posted on 04/08/08, 11:04 pm |
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You are not loosing your mind. Don't leg anyone tell you that. Your symptoms are real and they are vry hard to live with. I lost 45 lbs soon after being diagnosed. I was not trying to either. It just happened. I had so many people come up and say how wonderful I looked. None of them realized they were looking at a very ill person that was trying hard to claw my way through each and every day. Have you had your hearing tested? My neurotologist regularly tests me at least twice a year. He truly knows the challenges I face on a normal day trying to stay active and raise 3 kids. I've gotten used to living in a teeter wobbly world. It doesn't bother me near as much as it used to. No stinkin disease is going to get the best of me. My primary has been a good resource as he helps put all the pieces together where the ear guy only cares about my ears. Hang in there.
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your not alone honey. : ) I have to lip read all of the time. I have the tinnitus, low woosh in my left ear. I was offered steroid shots x 2 from my ENT Dr. recently. I am not sure but I think I may try it. What do you think? Keep your chin up.
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I have BPPV and have the same symtpoms. People talk to and comprehend one word. All the words seem to fall into one. I thought I was the only one. Hope you are feeling better.
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I don't get any dx yet. I will go to a different audiologist outside of Milwaukee area. I will tell you all the story much later.
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Thank God again for all of U as I have the same thing! I get hopeful that maybe my hearing's coming back but then it goes again:( I'm very grateful that I have a good audiologist as the ENT I saw is just awful!
I just wonder WHY the fluid in my ear increases at times and where does it come from? Does anyone else feel lots of pressure by their cheek/jawbone/ear? Mine gets so painful at times?!!
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This is also neuropathy issue... Your nerves are sending mixed messages to your brain.
Go check out this link and ask the same question there. http://dailystrength.org/groups/ne...
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thank god i am not crazy after all my family have accused me of faking my hearing loss as days i hear better than others, i wasn't aware that this happens i was afraid to ask my ent dr about this as i thought he would think i was faking too
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Honey I know how you feel. People get so mad at me when I ask them to repeat because i didn't understand what they just said. its so frustrating!
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You are not alone. My kids fight to see who sits on my right side ( my good ear ). The hearing in my left does change. There is more pressure and ringing right before a vertigo attack.
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