NeuroTalk Support Groups

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-   Multiple Sclerosis (https://www.neurotalk.org/multiple-sclerosis/)
-   -   Hi Newbys....Please Introduce Yourselves (https://www.neurotalk.org/multiple-sclerosis/4543-hi-newbys-please-introduce-yourselves.html)

SallyC 11-28-2008 11:37 AM

Nice intro, Roger..Thanks and WELCOME to NeuroTalk.(officially:D)

Thank you for your support so far and I hope you will let us support you, when ever you need it.

:hug:

MrsBones 11-28-2008 11:28 PM

Hi.

New to this forum...just joined! I found it through a post on another forum. It's funny, I recognize a few people from that forum and even one from Ravelry....I think, is that you Erin? :)

A few basics about me-
I have MS, live with my sweetheart of a husband, am a mom to four bunnies and I knit like a mad woman.

Looking forward to "meeting" you all!:grouphug:

SallyC 11-29-2008 10:06 PM

Hi Mrs Bones, and welcome to Neurotalk. Come on in and join your new Family. :hug:

weegot5kiz 12-07-2008 12:06 PM

Greetings to all of the new members, sorry for the generic greeting to all in one shot, I hope you have found threads to post on and ask your questions, Like i say in the welcome forum this place has some really wonderful, helpful and fun folks, and their friendships have been a blessing so many times, again welcome and do not hesitate to ask and or join in on the fun filled threads, we dont bite, well most of us but they got their shots so its all cool

seara 12-09-2008 11:46 AM

Hi Everyone....going through my second round of testing. First round was in 2001. Neuro sent me on my way with this statement "if it is MS, then it's a very mild case and you will most likely not have any more issues with it". :mad:

I was so disgusted I just went on about my life and lived it to the fullest. Now, 7 years later, I'm in an other exacerbation of something...whatever it is....and to be quite honest...this woman who is scared of very little is very scared of what is happening now.

But, I will do my research....I'll be seeing different neuro's and maybe we can get some idea what is truly going on.

I look forward to meeting ya'll and I wish you all the best.

:hug:
seara

SallyC 12-09-2008 01:10 PM

A great big Welcome to you, Seara..:hug:

Roadie47 12-09-2008 09:12 PM

Hello
 
Im Brenda aka Roadie.

I can't remember if I've been here before.

I have been being treated for m.s. for 8 yrs. I was on copaxone, but was just switched to rebif. Im scared to try it. I already feel crappy as it is, and don't want to feel worse. any thoughts?

Nice to meet you all. I've been a member here for too many yrs to recall.

SallyC 12-10-2008 12:53 PM

Hi Brenda and Welcome to NeuroTalk... Pull up some velcro and stay awhile.:)

I'm the wrong person to ask about the shots. I swore off off all poisons, years ago..:D.. I did give Avonex and Copaxone a try, though, I've not tried Rebif (just a stronger version of Avonex)

Come on in and start a thread about it and many Peeps will come to your aid and answer your questions..

Again, Welcome..:hug:

Riverwild 12-10-2008 06:42 PM

Hi MrsBones and Seara and Roadie and welcome to NT, even if you have been here before!:)

Snoopy 12-11-2008 09:47 AM

Hello, MrsBones, Roadie, and Seara and welcome to NeuroTalk :)


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