Hi Hopeless,
Would it be ok with you if we exchanged emails? I would really like to have someone to talk to about MP. I am suffering a lot right now, because all of the doctors are on vacation due to the christmas/new year's holiday period. I would really appreciate advice from someone who has been through this.
If that's not ok, I can just keep posting to you here.
Quote:
Originally Posted by Hopeless
Hi paperbag,
There are a few of us still around but many MP sufferers come and go because for many it is a short term problem and they recover. That is the good news. I guess a lot depends upon the "cause" of the MP. MIne was due to damage of the LFCN during a surgical procedure and I have been dealing with it for about 35 years. If you wish to talk more about it, I would invite any questions you may have. A lot of us know the misery of being undiagnosed, mis-diagnosed, etc. on many neuro conditions so we can relate.
I am here for you any time you want to talk.
Hopeless
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