Hi Jay! What part of Georgia are you in? Do you have a diagnosis of MS or of anything in particular?

The MS Center is in Atlanta. Also Emory is in Atlanta and probably has a good referral service.

Welcome to NeuroTalk!!

Newbie from Saskatchewan (Canada)
 

Hi everyone, I'm not really sure whether or not I belong in this forum, but I'm not sure where I belong...in terms of a health category.

I am currently under the care of a GP, an ophthamologist, and a neurologist. All have mentioned the possiblility of MS, but they don't have real "proof" of anything...and I'm not sure that much else has been ruled out, either. I've had two (relatively) clear MRIs in the past two years, but I have Babinski's sign in both feet, and a few other obvious signs and symptoms. I'm scheduled for two types of evoked potentials tests on July 13th, 2009. I hope that something helpful shows up.

...in order to share why I'm here, I've included (below) the general info that I used in order to introduce myself on the main "welcome" forum a couple of days ago:

I don't have a diagnosis yet, but have several symptoms that are neuropathic. In the fall of 2007 I developed double vision. I've also been having muscle twitches for more than 3 months now...every day, all day. I get sharp 'electric' type pain sometimes down a limb. Sometimes my feet go numb, sometimes my hands tingle. I have had a rash on my face for about 10 years now. I was told it was rosacea though. I have some hair loss too. There's more, but I think those are my main symptoms.

My mom has primary progressive multiple sclerosis. She is 56 years old and has lived in a nursing home for 10 years already. I have two aunts that were diagnosed with SLE (Lupus)...both on my dad's side of the family. One is struggling with lung problems mostly, and the younger aunt (58 years old) passed away due to Lupus in April 2009.

I don't know what I have, but it would be nice to find out. I'm hoping to learn from those on this forum...about their lives and the roads to (and beyond) their diagnosis.

Kind regards,

Jayne

Hi. I made a post about my issues and concerns before I saw this.

My name is Jessica and I am from WV.

I am in limbo and I am lost and confuzed.

and I'm really depressed about my mood. NOt to be so gloomy but I am never happy anymore so I am worried that this situation is running my life or if it a side effect fo whatever is going on with me.

Anyways, I am teacher, just graduated from college. But taking some time off again. I have a daughter who will be 4 in August and I am married.

Nice to meet yall.

Hi Sask, nice to meet you and welcome to your new home. I'm so sorry for all your troubles and pain. Limboland is the worst, but we are all here to help each other thru the tough times, so anything we can do to help, just ask.

Join right in anywhere and be sure tro visit the Stumble Inn for a little fun. :hug:

Hi Ya Shortfusion...hehehe, I love your nick..:D I hear you, with the worry worry stuff. It's darn hard to be happy with this carpola hanging over your head.

Come on in and join your family away from home and let's see if we can put a smile on your face..:hug:

Hi SaskMom and shortfusion!

Welcome to the place you never thought you'd be in! Make yourselves at home! Ask questions and someone will answer. We've got lots of folks with lots of experience here!

If anyone sees a sweet woman from Kentucky come in here let me know. Jim and I met her while in Kentucky at the Cracker Barrel. Her hubby looks like George Jones. :wink:

Hi All. My name is Jen. Today is my first visit to NeuroTalk. I was diagnosed with MS in Jan. of 2007.

I live in Corning NY with my husband Adam. We have a 6 month old daughter named Hannah and a dog named Fred. Hannah is the best thing that ever happened to us!!

I work in early stage 1 research as a polymer process technician. I know you're probably wondering what the heck is that. My background and education is in Chemistry. I work in an organic lab with plastics.

I'm currently taking Copaxone. Nobody loves a shot, but it could be worse.
I'm very happy that I found this site. I've already learned a few things in the last hour browsing the threads, so let me just say thank you. :)

Welcome to Neurotalk, Jen. I'm glad you found us and decided to join us.:)

Your profession sounds interesting....tell us more. :cool:

Just join in anywhere and enjoy..:hug:

New!
 

Hi there... I'm new to this site and new to MS. I am 24 years old. I was dx last December 2008 with RRMS with symptoms that started 3 months after giving birth, so January 2008. I have had two attacks since but am doing well today. I was on Copaxone for a bit but had problems with the injections. Severe reactions at injection site. I will be starting a Phase III clinical testing in 2 weeks called Teriflunomide.

I'm greatfull that sites like these exist and look forward to keeping up with many relevant discussions!