How do I become a member of this group or any other group for that matter?I'm having a little trouble figuring things out being a newbie and all.

You're in, just talk. We have no initiation rights.....we are a mellow bunch.

LOL thank you.I think I got confused because my post wasn't posted right away.

Suggest that you go to the top of the forum and read Forum PN Tips...
http://neurotalk.psychcentral.com/forum119.html AND
the 'Forum Sticky's' at the top of the forum posts/threads....
Both will give you a base of info about various PN's? AND then read previous posts and decide which aspects you can learn from. [Other than diagnosis and treatments is NOT EASY!]
Don't be afraid to ask questions! No question is silly or too simple for us! We've all had to learn the same way and share and aren't shy. Hope you aren't too shy either?
Keep learning! You've friends here, and support! I KNOW I've gotten more help here than anywhere else!
Hugs 's and hope - j

Welcome to the party.
You've found a great place and you'll soon see this forum is packed full of caring people and much MUCH knowledge.....

Here's the "New Member Intro" forum if you wanted to post there....
I think you mentioned something about that...

http://neurotalk.psychcentral.com/forum88.html

Glad you're here!
Rae
PS if you don't see your posts right away, it's because new members posts are filtered thru the admin B4 they go straight to the board....
Which is yet another reason this place is so wonderful (and safe!) .....no 'spam'...... but that's yet another whole discussion
Stick around and you'll see......... we all just LOVE our spam-in-a-can

Thank you,I think I'm getting the hang of it.I just finished reading someones story of their neuropathy journey.Very interesting.I'll probably be around for a while.All signs point to sfn for me because I just remembered at the beginning of last year the emg specialist said I have a touch of neuropathy on both tests and my current neuro believes with their results being slightly abnormal that I may very well have sfn.I already know I have POTS and autonomic dysfunction without a doubt,I just need the actual tests to prove it which will be on June 15 but I keep calling to hopefully get in sooner.I will have the tilt table and sweat test.Why they don't just do the biopsy and get it over with is beyond me.I'm not going to post on the actual new members forum.I'm only interested in this board for now until I figure this site out.Thanks for all the useful information and links.

Welcome!!!


Phyllis