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New members should feel free to introduce themselves here

Hi * !

After browsing for almost a year now, I thought it was time to join.

I'm a male 36 from The Netherlands...

First I want to thank all involved in ThisIsMS. This site stands out with head and shoulders above the rest. It's really informative and a decent MS-library.

I've been diagnosed with RRMS after a Nuritis Optica. That's now 4 years ago. I had some symptoms before but never realized it was MS. I'm pretty ...
Read more : Hi * ! | Views : 1834 | Replies : 9


New Member, newly diagnosed

Hello All,

My name is Chris and I have been recently diagnosed with rrms. For me the first attack I had was optic neuritis on 2002, and at that time they did a scan of my brain and the results were negative. My vision came back and I went about my life. Keeping it in the back of my mind because my mother had MS in her life.

Now, about two months ago I went ...
Read more : New Member, newly diagnosed | Views : 1500 | Replies : 3


Hello all,,,

HI every-one,
I am new to the site. I am still under investigation;I have had an MRI, EEG. Scan on the head, IQ test' to see if my brain still works!! Have to find it first lol;
Bottom line still not dx. I am 50 years old have two daughters and am divorced. I live in London I am a prefessional hairdresser by trade and have had my own business. Over the past 6 years ...
Read more : Hello all,,, | Views : 1756 | Replies : 6


Hello Everyone....



My name is Annie a/k/a "Kittikat." I'm new to the forums. I was dx'd with RRMS last May of 2005. I'm currently taking Copaxone along with other various meds to control symptoms.

I am currently working (part time) as a veterinary receptionist and I really love my job! However I get extremely depressed many days because I am so exhausted and in such pain when I get home. Even just from part time. Even ...
Read more : Hello Everyone.... | Views : 1447 | Replies : 5


Hello!

Hi,
My name is Jenn, and I was dx'd with RRMS a year ago. I started Avonex about 5 months ago, and am happy with that decision so far. The relapse that led to my dx was severe, and I now use a walker or cane if I'm not at home. I can't drive much anymore, which stinks, but I can live with it.

I am 30 years old, married for 7 yrs, and we ...
Read more : Hello! | Views : 1632 | Replies : 7


Hello, 3 mo from diagnoses in Seattle

Hello.

I am 44, widowed, and a college student. I got the 21 gun salute for my final acknowledgement of MS. I had been denying it for some time. My sister has it. So it took a 2x4 to get my attention. Carted out of work. In the hosp for 22 days. Now I am on welfare waiting on disability.

It could be worse. I found out how very many real friends I have. People ...
Read more : Hello, 3 mo from diagnoses in Seattle | Views : 1399 | Replies : 2


Hello, Newbie Here

Hey! My name is Eliza. I just was searching through the web and came across this site. This looks liek a nice site and with some helpful information about MS so I figured I'd join.

A little about myself: I am married and 33 years old. No children yet, but I have two dogs if that counts as children :). I was diagnosed with MS in 2003, ...
Read more : Hello, Newbie Here | Views : 1717 | Replies : 5


Would Like To Say Hello

Hi, my name's Nina, I'm 50 and waiting to be diagnosed after a very long wait.

I hope you don't mind me being here but I'd really appreciate any help I can get to help me on my journey.

It's quite a site here!! It will take a bit of getting used to but I'd like to stick around if you'll have me.

Take care all. :D ...
Read more : Would Like To Say Hello | Views : 1356 | Replies : 3


My Introduction...

Hello. I am a thirty-seven-year-old wife and mother of two boys, ages five and ten. I was diagnosed August 8, 2006. MS sucks.
Read more : My Introduction... | Views : 1619 | Replies : 8


New from Dayton, Ohio

Hello All,

I'm Lew Chapman from Dayton, Ohio. I am a 40 year old, white male that has had MS for 5 years now. I'm very high functioning in that none of my symptoms affect my motor ability now. I have horrible Optic Neuritis, bladder and bowel issues and lots of tingling and numbness. The only thing that approaches debilitating is when my bladder makes me pee every ten minutes. And truthfully I would call ...
Read more : New from Dayton, Ohio | Views : 1617 | Replies : 5


 

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