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New members should feel free to introduce themselves here

Hello there!

Hi there from PA!
"Oh, But you you look so good!"
I was Dx in 2001 with RRMS after being paralyzed from the neck down. I regain feeling and then use of my arms within a few weeks. It took me though a few years to get back up on my feet and walking again. To look at me now, you would never know what my body had been though!
I am a support group ...
Read more : Hello there! | Views : 1471 | Replies : 0


Hi All

Hi everyone....glad to have found this site!

My name is Steve, 40 years old, and diagnosed with RRMS back in December following a fairly debilitating attack. I've been lucky enough to enjoy good health for my entire life, having rarely ever seen a doctor until a few months ago. Unfortunately, all of that changed back in late November.

Right around Thanksgiving, I noticed a tingling/burning in my left leg, and I recognized the sensation as ...
Read more : Hi All | Views : 1543 | Replies : 3


New to the Site

Hello to all!

I just came across this site - and am eager to get into it more! I've been diagnosed for a year and a half - after a 5 year struggle! Just started Avonex, also on Lamictol. Most days are great, but some days really really suck!

Glad to be here! Any advice welcome!
Read more : New to the Site | Views : 1704 | Replies : 2


Would appreciate new friends/contact

My name is Cindy and was diagnosed with RRMS in early 2002.
Have been reading this wonderful forum for several months... this is my first post. Just turned 51, I am in North Carolina, originally from CA, USA.
At this stage, there is no pain but my mobility is really bad.
I'm not sure what I want to say--other than I just have to get started and actually reach out/connect this time...
The bottom line, ...
Read more : Would appreciate new friends/contact | Views : 2537 | Replies : 10


hello from Boulder, CO, US

Hi everyone,

I'm Trish. I've been dx'ed for about 9 years. In two weeks I'll have my 7th or 8th Tysabri infusion. I had previously used Copaxone, Rebif and Novantrone without good results. The depression from the Rebif was unbearable.

Tysabri has been good for me so far. I have not had a serious relapse since I started it. I've noticed that I have kind of lost my appetite and I've lost about 15 - ...
Read more : hello from Boulder, CO, US | Views : 1981 | Replies : 5


New with questions

Hi all,

I've been reading this site for a while and have found alot of really good info here. I decided to finally post because I had a couple of questions and was wondering if anyone has had a situation similar to mine.

I was diagnosed back in 1996 at age 22 after a pretty bad initial attack. After I recovered from it, I regained all of my function/mobility except for a few remaining pains, ...
Read more : New with questions | Views : 1799 | Replies : 3


Newbie

Hi! I am Jyn.

I found this site last night after searching for troubleshooting tips on my Rebif auto-injector (I posted my issue under the Rebif subject) and I have enjoyed reading the many posts and articles.

I was diagnosed 3 years ago when I was 29 years old. Mostly my vision has been affected: Optic Neuritis, Double Vision, Vertigo. Otherwise, this disease has definitely played havoc with my cognitive abilities. Have you heard of ...
Read more : Newbie | Views : 1976 | Replies : 5


Hi, I'm Breeze

Hi - I hope I am doing this correctly..My name is Breeze and I just located this website. I am an RN on retirement disability thanks to "You Know What". I am married, have three grown sons who are off into the world. I am on Betaseron d/t experiencing site reactions from Rebif after a few years. So far, so good. Well, I'm off to see if this works. GWG
Read more : Hi, I'm Breeze | Views : 1755 | Replies : 3


Greetings...new to the place

Just passing through to introduce myself. :P
Read more : Greetings...new to the place | Views : 1580 | Replies : 0


hello and thanks for all the info and support

hi. I have been visiting (lurking, researching, exploring) this site since last summer in support of a v. dear friend who finds it all too much to absorb, think about, handle on her own. You have a fantastic site and group of people here and the stories and information you share has been incredibly helpful to both my friend and myself.

Right now I am researching what some options are as her RRMS shifts into ...
Read more : hello and thanks for all the info and support | Views : 1587 | Replies : 2


 

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