--- In menieresdiseaseclub@yahoogroups.com, Kopperbug <kopperbug@...>
wrote:
>kopper,
depression can be more than just a litte,, this disease
can play tricks on ur mind!!! i forget so much i get scared
that i'm getting that alzthtimers<sp> thing
but after talking to others,, i find they forget alot too...
sure helps to talk w/ others that know w/ ur going thru !!
good luck w/ mayo clinic-- hear they're
pretty good..
bonnie,, keep posted
> I have decided to go to the MAYO clinic. maybe they can help me
without destructive surgeries or controversial surgeries. I will be
flying to minnisota in the spring to see them. I couldnt imagine
having this for 7 yrs. I was dx in march 2006. and already so much
hearing loss and so much damage. at one point i think i might have
had a touch of depression due to the life changes.-especially home(
3kids) and work and having to stop school. now im back in school,
struggling, and back at work full time, struggling.
> lol. my mother always used to say that i liked to make things
difficult for myself. now its my own body thats the cause. she had
this disease too and i didnt know til after i found out i had it.
she's been gone for years now so i cant ask her about it.
> I hope to have complete internal acceptance and glad you have it
now.
> keep it dizzy free ~smooches~
>
kopper
>
> beebee442000 <no_reply@yahoogroups.com> wrote:
> --hello,
> my name is bonnie. i've had mm for going on 7 yrs. i'm deaf in the
> rt. ear & going in lf.
> had the shunt,, didn't help,, as have heard from most others too.
> but we are all different,, so it could work for u..
> i had the nerve section & another surgery,, too long to explain,
> right now-- but i dont regret them.. i was on the verge of suiside
> and i'm not kidding. BUT i had a very bad case.
> now i have it in good ear.,, nothing to do , except when lose
> 'all' hearing is the implant/ which i'm hoping doesn't happen,,
> but am losing more hearing every day..
> reply when you can
> wishing you better days
> bonnie
>
> - In menieresdiseaseclub@yahoogroups.com, Kopperbug <kopperbug@>
> wrote:
> >
> > All these procedures like labyrinthectomy and destroying the
> mechanics what about people who have this horrid disease
bilaterally?
> my doc is against doing anything destructive due to it being
> bilaterally. i dont know what do next. i miss so much work and time
> with my family. i just want to be normal again. the doc said
> something about a shunt and that maybe that would work for me. I've
> heard of this in the past from someone talking about it on here
> although I didnt pay much attention to it at the time. has this
> worked on anyone? please do reply. thank you, kopper
> > to dizzy free days~
> >
> >
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