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New members should feel free to introduce themselves here


..the one and only Cyclops!

Hi everyone. I'm new. I chose the name Cyclops as that's how I feel right now. I was diagnosed 6 months ago after getting a dose of optic neuritis which still hasn't cleared up. I've been reading your posts and following your stories and felt it was about time I joined the club.

One-eyed smiley - like it?

Read more : Introducing... | Views : 1627 | Replies : 5


I have been lurking on the site for yrs. DXd 5 yrs ago w/MS; RRMS or PPMS was not determined @ that time but it looked progressive. I had been experiencing symptoms that clearly indicated something was WRONG for 2 yrs before breaking down and dealing w/it. My early symptoms, foot drop mainly after strenuous exercise, seemed like they could indicate not only MS, but ALS or Parkinson's. My feeling was, I am in no ...
Read more : Hello | Views : 1383 | Replies : 3

"New" to it all

Hi everyone,

Well, "cheerleader" mentioned I should post here I am!

I recognize some names here from another hi!

This is long...but I realize as I sit here, nearly 4 months into this out-of-the-blue random diagnosis....I will share...

Let's see - I'm new to ThisIsMS and MS altogether.

On December 22, 2007, the right side of my face started feeling weird - within a few days, it was entirely numb from chin ...
Read more : "New" to it all | Views : 2018 | Replies : 11

late introduction

hey, I am sorry, I've been to this forum for some weeks now and forgot to introduce myself...
my name is veronika and I'm from Slovenia. I have been diagnosed 4 years ago and have been taking rebif for 3,5 years and have now started tysabri on 21/4 but have had a serious relapse since and I can now hardly walk (have had trouble walking for 1,5 years but not so severe and twice problems ...
Read more : late introduction | Views : 1726 | Replies : 7


Hi another newbie here from the UK. Diagnosed RRMS Feb 4th 2008. Started Wheldon CAP Protocol April 20th. So far, nothing's dropped off. :wink:
Read more : Hellooooooo | Views : 1694 | Replies : 5

New here, from Texas

I just wanted to say hi, and I've just found this site.
I was dx in Feb. 07 and I am in the Tovaxin trial.
Would love to hear from other Texans on this site as well.

Read more : New here, from Texas | Views : 1781 | Replies : 9

Hi Everyone

I hope everyone is having a great day. I need the help of everyone out there. I know I introduced my self the other day. I told you about the auction we are having to raise money. I really need the help of everyone to pass the site on to people who could afford this Cycle we have up for auction. It was my biggest donation! I know it's a lot of money but someone ...
Read more : Hi Everyone | Views : 1276 | Replies : 2

newbe here

Found this group today.
Have had "possible MS" since 1969. Relapse and new tests 2004 with definite DX of MS. Was on Betaseron for almost 4 years. Really bad relapse in Dec. 2007. Changes to Copaxone and had a bad reaction on day 4 & 5 of it.
Was told to stop it. Then it took several months and new MS neuro specialist to get me started on Tysabri. Had my first infusion on April ...
Read more : newbe here | Views : 1239 | Replies : 0

Hello from Pennsylvania

Hi Everyone,

I am a mom with MS. My kids are wonderful and they keep me going every day. Without them and my husband I don't know if I could make it day to day.

I am glad to have found this forum. I have 2 reasons for joining. First to talk with other about MS and day to day things. The other is I am always raising money for MS.

We are doing the ...
Read more : Hello from Pennsylvania | Views : 1040 | Replies : 0

I´m new here

Hi there

I´m looking for some answers to the symptoms i´m having at the moment therefore i found this forum which looks very good with plenty of information. :)
Read more : I´m new here | Views : 1172 | Replies : 2


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