[Dejibo]

hello and welcome to all the new one.

[kathie1026]

Marge, I've suspected MS since my symptoms started Jan. 2013, however, I was just dx'd with "conversion disorder" this week. Not sure if he's right, but time will tell.

Originally Posted by mhill62

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

[Old Gal]

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!!

[SallyC]

Hi Old Gal, welcome. I bet I'm older..
I was DX in 1976..

I'm so glad you found us. Come on in and join the Whine and Cheese party. We all understand where you're coming from and are here to support you.

[hunibuni]

Hi everyone I have peripheral neuropathy and my symptoms for months have gotten worse. They now include more pain fuzzy head spasms in my feet heavy legs which go tight when walking weird nerve feelings in my face like wearing an invisible eye mask lack of sleep concentration level not the same. I went back to doc today again and was told i am still waiting for neuro surgeon referral which i have been waiting two months so far. I am getting so frustrated with it all and have no support

[Kelfelton]

My name is Kelly and have been experiencing symptons for a month now. Worst thing is my hands! They feel as if I've been holding snow balls for over an hour and have frostbite. Other symptoms (numbness and tingling in my feet and numbness in my entire lower body as well as the girdling around my mid section) have decreased somewhat in the past week. An MRI of my brain has apparently shown myelin evident in the brain so my primary doc called me this evening to give me the news. Still going to follow up with a neurologist to see where to go from here. Looking forward to getting good info and support here! Thanks!

[SallyC]

Hello Kellie and welcome. So glad you found us. Ugh, the diagnosis process begins.
I hope it happens fast for you. It sounds like your Doc has found signs of MS.

You are in the right place for understanding and support. Please let us know
what your Neuro says.

Good luck and good wishes..

[Kitty]

Hi Ally and Old Gal! Welcome to NeuroTalk! Make yourselves right at home and join in the discussions. Also, The Stumble Inn is a place for MS folks to gather and talk about stuff that's not MS related. Here's the link http://neurotalk.psychcentral.com/forum102.html.

Good to have you here!

[Tigerlilly]

hi, just introducing myself. Its my boyfriend who has MS. I'm the active one on our relationship always researching and reading up on his condition. We hardly talk about it, as that would make MS more 'real'. But he trusts me on everything I tell him lol. Wish he would become more involved in his own health. oh well. I'm glad I found this forum!

[Kitty]

Welcome to everyone who's new! Join right in on the forum....lots of good info and nice people.