[pinkgemi]

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!

[mrsD]

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.

[GAM1211]

Originally Posted by pinkgemi

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!

Hi Pinkgemi. my name is GAM1211 and I was just diagnosed with MP.
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.