Welcome Cookie, nice to have you with us. These are the nice accidents that happen, even though your reason for being here sucks..:hug:

I hope you like it here and stay.:)

Hi my name is Christy and this is the second time since 2009 that I have been told that I may have ms the waiting game and the no answers make me feel like I am crazy and everyone around me has been thinking it is all in my head!!

Hi Christy, welcome to the, it's all in our head club.:D

Come on in and join in anywhere. We are all here to help each other through the bad times and have a laugh with each other through the good times.

Glad to meet you and have you here..:hug:

I like this site
 

Just signed up the otherday - lots of great info here.

I have had MS 5 years now -- plus a few other things. Just started having spasms -- they are trying awhole bunch of meds, been looking them up here.

I hope to post something after a few days and report what works for me or what might not work.

Hi and welcome to NeuroTalk, mgarneau! :welcome_sign: Pull up a chair and join right in. There are lots of friendly folks here and lots of good information.

Welcome mgarneau, nice to meet you.:)

Newbie from huntington beach, ca
 

:confused: new to sign up. I've lived with ms for many years and overall, I do ok. I'm starting to get older now and would like to connect with some older women who have ms and have managed the female aging process. I'm also interested in learning from others who push back on this disease and maybe I can offer some of my own stories and perspectives of ms management.

Hi and welcome to NeuroTalk, hbjro! :Wave-Hello: Nice to have you here. There are lots of women on our MS forum and we'd love to share stories with you. There are even a few men.....and we let them in most always. ;)

Welcome to your new home away from home, hbjro:)

Aging and MS. Fun, isn't it? :mad:
I'm 70something and had my first apparent MS symptom at age 24. Do I count..:D
Still can stand up, but not much walking. In my Scooter, mostly, these days.

Aging and MS are two life altering events, together, it's a catastrophe..:eek: Not that bad on most days. Read the Accomodations Thread inside!!!!

Come on in and enjoy..:hug:

very tired
 

Hello, I just found this page today. I have been diagnosed since Jan 2009. From my MRI's, probably had a couple years before I was diagnosed. I have been very blessed to do as well as I have. I am struggling with major fatigue right now. All I want to do is sleep. My body just feels weird. Started with really bad headaches. I am getting a new MRI of my Brian in the next couple weeks to see if there are any new lesions. Hoping there are none, but at the same time, hoping there are so that would be the reason I feel so bad.

My last attack was in Oct of 2010.

I do have a very stressful job, trying to learn how to not let it stress me out.