[beccie122]

hello everyone, i'm new here.
my name is Rebecca and i know for about 2 weeks that i have small fiber neuropathy.
the doctors gave my pills for the pain, but the still don't work..!

it's still a little bit hard to believe that i have this disease,even so its a family disease, my mother and aunt have it also.

greetings from my

[Abbie]

Hello Rebecca and WELCOME to NeuroTalk!

Here is a link that may be of assistance to you... I hope. (I'm not well versed on the different types of Neuropathys.)

Peripheral Neuropathy
http://neurotalk.psychcentral.com/forum20.html

Please feel free to roam around and join in anywhere! If you have any questions or need any assistance please don't hesitate to ask...someone will always be along shortly to help in any way that we can...

I look forward to seeing you around the board.

Abbie

[MelodyL]

Originally Posted by beccie122

hello everyone, i'm new here.
my name is Rebecca and i know for about 2 weeks that i have small fiber neuropathy.
the doctors gave my pills for the pain, but the still don't work..!

it's still a little bit hard to believe that i have this disease,even so its a family disease, my mother and aunt have it also.

greetings from my

Hi there.

You have been given the right forum to go to.

I am sure if you post any questions, others will come along and help you.

We are a very friendly group of folks.

Welcome!!!

Take care, Melody

[Darlene]

Rebecca,

Hello and welcome to NeuroTalk. Happy to see you have come to be with us. Just let us know if we can be of any help.

There are great number and caring fellow members here, just let us know how we can assist you. Our shoulders are here for support in many ways. You see we are are supportive and relaxing place to be.

Again welcome, looking forward to seeing you around. My thoughts and prayers are with you.

Darlene

Originally Posted by beccie122

hello everyone, i'm new here.
my name is Rebecca and i know for about 2 weeks that i have small fiber neuropathy.
the doctors gave my pills for the pain, but the still don't work..!

it's still a little bit hard to believe that i have this disease,even so its a family disease, my mother and aunt have it also.

greetings from my

Greetings, Rebecca, & welcome to NeuroTalk. I hope you're getting over the shock of your diagnosis. I know how hard it is in these early days; you keep thinking that you'll just get a phone call, someone will say the labs were wrong, somebody made a mistake ....
I hope you come back & let us know how you are. We want to help.

[(Broken Wings)]

Welcome to NT

I hope you're finding your way around. Let us know if you need help.

There's lots of info here.

It can be overwhelming when you find you have medical problems.

Although we cannot diagnose, we certainly do understand.

I pray all is going well for you.