Hi Ruthie and welcome to NeuroTalk..:)

So sorry as to why you are here, but glad you found us. There are quite a few still in Limbo, here, and us oldsters can help you along the way to DX.

Join right in anywhere and be sure to visit our Stumble Inn for a bit of comic relief.:)

:hug:

Hi Ruthie and welcome to NeuroTalk! Some here have had to wait quite a while for the diagnosis. I'm glad you joined us.....hope alot of your questions can be answered while you're waiting. Between us all there's many years of MS experience here! :)

http://i489.photobucket.com/albums/r...s/surfing2.jpg

Hello PL and Ruthie, and welcome to NeuroTalk and the MS forum. This is such a great place with lots and lots of friendly and very helpful people.

We're so glad you found us!

Be sure to check out The Stumble Inn for non-MS topics.

http://neurotalk.psychcentral.com/forum102.html

Also, Games and Such is a lot of fun and can help take your mind off your problems for awhile.

http://neurotalk.psychcentral.com/forum104.html

New to the chatbox here.
 

I have many questions about MS and some of its effects.

I am new here but not to MS. It has been living rather silent for a few years and then suddenly it was all over my life....again.

I am looking fwd to finding some of the answers and advice here.

Thank You for offering such an informative place for those of us in need.

Welcome to NeuroTalk, HHChick, nice to meet you..:) So sorry that MS has raised it's ugly head for you.

Join in anywhere here and glad you found us.:hug:

Thanks for the warm welcome Sally..and the nickname........

Signed,
HHChick :D

Hi HHChick and welcome to NeuroTalk! I'm so sorry that MS has decided to invade your space but I'm glad you found this site. We have a good time here and support each other throughout the ups and downs of this confounded disease. I hope you'll post more so we can get to know you better. If you have any questions just ask any one of us here and we'll be happy to help you. :)

Hi Everyone!! I was just diagnosed 2 months ago and just started with Copaxone last week...so far so good!! My situation is a little unusual I think because I don't have any symptoms right now but some tingling/numbness in the past coupled with 2 MRIs that showed active lesions resulted in a diagnosis. I'm curious if there are others on here that are in the same boat - the meds are always way more troublesome than the disease! Good luck everyone!

Hi Everyone!
 

I was diagnosed 2 months ago and have been on Copaxone for 1 week - so far so good! I am curious if there are others on here with my same situation - I have no symptoms at present but was diagnosed due to tingling/numbness in the past coupled with 2 MRIs showing active lesions. The cure is sooo much worse than the disease...at least for now. So far the Copaxone is going great but I hope I don't have to go back on Solumedrol..that was rough...I'm looking for to "meeting" all of you!

Hi Kats, welcome to NeuroTalk, nice to meet you. Please come on in and join us.

You are so lucky to be in remission right now.. I'm a firm believer in, if it ain't broke don't fix it. In other words, no DMDs if you are having little or no symptoms. That's just me...everyone is different.:)