New Members To The MS Forum....Please Introduce Yourselves!
 

Since the original "New Members" thread (http://neurotalk.psychcentral.com/thread4543.html) had gotten past the 1,000 post mark we're starting a new one.

New members to the MS forum please introduce yourselves here so we can welcome you! :)

Thanks Kell, I showed this link in the old one, so Chamar can make it a sticky..:)

please introduce yourselves
 

Hello, I am new. Trying to figure out what is happening to my body since this past March. Intermittent stuff, now not so intermittent. Don't know where to start.. thought the place would be with Dr's but is going nowhere. Thank you, Marge

Hi Marge, if your doctor isn't listening please find a new one. If you are having symptoms and feel MS needs to be looked into then you need to see a Neurologist that specializes in MS.

I'm sorry you're having rough time.:( Welcome to the group:grouphug:

Welcome, Marge.:) This is an MS Support Forum. Do Drs here, unless they happen to share our MS.

I understand your confusion and fear.:( It sounds like your Doc is not helping you. If you susspect MS, then look for a Neuro who specializes in MS.

Let us help you through your diagnosis process..:hug:

Hi Marge and welcome to the group! :welcome_sign: I'm sorry you're not getting anywhere with the medical community. Sometimes it seems like an uphill climb to try and get anyone there to listen. :rolleyes:

I think you'll find lots of support and information here to help you along the way. Hope to see more of you here!

hello and welcome to all the new one. :hug:

Hi all!
 

Hi!!!!!

I'm Ally, I've been struggling to get a proper treatment for over 4 years. I finally got a little bit of a breakthrough and have an appointment at the MS research clinic at UBC next week. hopefully things are looking up :)

Welcome to NeuroTalk Ally, nice tp meet you..:) Have you been diagnosed with MS?

I hope you get all the answers and proper treatment you need from the UBC Clinic.

Stay with us and let us know how it goes.:hug:

New To You
 

Hello everyone! I was diagnosed with MS in '97 and have been on Betaserone ever since. My MRI's haven't changed much but I have gotten more and worse symptoms. Have any of ya'll ever heard of pudendal nerve entrapment? MS is rotten enough without having the ignominy of this !!!!! I won't even talk about the pain cause I bet every one of you has thier own little "Shop of Horrors" when it comes to pain talks. :( It is nice to find a place where like minded folks can talk about things. I hope to talk to each of you soon......Happy Trails!!