ANA Discussion Forum
Post-Treatment => Balance Issues => Topic started by: jerseygirl on August 08, 2007, 07:33:40 pm
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Hello everybody,
Here is a device specifically to help balance. Is it for ANers? NF-2s? Can you do periodic MRIs with it implanted?
http://www.sciencedaily.com/releases/2007/08/070806112548.htm
What does everybody think?
Eve
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Hi Eve,
What an interestng article, it sounds promising. That would definitly help a lot of people. Now the trick is to get it approved and make it smaller. Thanks for the information. Ann
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Wow... and under a millisecond too.....
Thanks,
W.
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Very interesting article. It's funny how a lot of articles about hearing aides and other developing aides don't mention AN's. I wonder if it is because there is a difference in the stability of the region where the AN is or what?
Brendalu
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Brendalu,
Nobody mentions AN, you are right. Also, nobody is concerned with periodic MRIs but that would be the problem with everybody since now there is such reliance on MRIs.
Eve
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Maybe noody mentions us because we are such a rare breed??? Too bad we aren't an endagered species,eh??
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Facinating!
Rob
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Wow, that's interesting....I was just about to post something else I found on balance, so I will keep it in here. It is a new device as well. Then there's also the brainport. Anyone out there tried any of these?
http://www.cnn.com/2007/HEALTH/08/10/stroke.treatment.ap/index.html
Eve, I find it really interesting in your article about orientation, because I feel that's my main issue....get too many moving objects around me and I become disoriented and that makes me lurch to the right...it's not at all vertigo or lack of balance, if that makes sense.
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It makes perfect sense and we can exercise only so much before it eats away at our personal time. This article really hits it on the nose while desribing what people with cut vestibular nerve feel.
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Gennysmom,
The article you posted is fascinating. No, I haven't tried any of these devices, just good old fashioned Yoga, Pilates, treadmill and free weghts but you have to be regimented with exercise. Too much and you get headache, too litle and it does not work.
Eve
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Eve - yes, and add working full time post microsurgery in the mix, and let me tell you, exercise is hit and miss. I can do stuff for a week, then I crash, pick myself up at some point, try again, crash.....it's a bad cycle. I'm in crash mode right now. 2 weeks ago I probably put about 20 miles walking in. Today I couldn't get a mile done. Tomorrow, who knows? One day at a time!!! ;)
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Hi Eve;
Thank you...
I had seen the device advertized soon after JHH released it's study information to publications and maybe the press.
My feeling is the device sounds very promising and exciting, especially to younger folk whether with AN or other type ear problem.
I also feel if the device is ever released by the US FDA, it will literally floor Wicab Corp. and their "Brain Port". Of course the FDA has not released Brain port to the US public that I'm aware of, but are continuing their studies. Brain Port can be purchased in Canada and EU, I believe.
Have a great week!
NF-2er