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06-01-2010, 11:47 AM | #1 | ||
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i am trying to find out if anyone still active with this forum? I have mp and would like to share my story with others, but want to make sure that people are still using this site!
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06-01-2010, 12:20 PM | #2 | |||
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Wisest Elder Ever
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Welcome to NeuroTalk. Some posters with MP also post at our Peripheral Neuropathy forum.
http://neurotalk.psychcentral.com/forum20.html I had this for many years, and I confess I don't follow this forum often anymore either. I found relief finally with Lidoderm patches. There is a lidoderm thread there too. http://neurotalk.psychcentral.com/sh...light=Lidoderm I would post your story here on this forum anyway, because visitors come from Google all the time, and some just read.
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All truths are easy to understand once they are discovered; the point is to discover them.-- Galileo Galilei ************************************ . Weezie looking at petunias 8.25.2017 **************************** These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here.
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"Thanks for this!" says: | Rrae (06-01-2010) |
06-03-2010, 09:58 PM | #3 | ||
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Quote:
I guess I'm part of the 'classic' description, overweight and diabetic. I've also had knee replacement (left) and have the MP for about 3 months. It's taken that long to diagnose. Just started with Neurontin today. Took it several years ago for shingles pain. Kinda familiar with side effects. Would love to hear your story, and any help notes you may have gained with the disease. God Bless. |
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