About me: This website is dedicated to all those who have M.S. and are not in the common age group. Instead we are teens and young adults facing a life-long obstacle each and every day we go out. This site is open for discussion, questions, and mostly moral support to let all of the younger people who have M.S. know that they are not alone.
Who I'd like to meet: Any one who has this obstacle in his/ her life.
Just here to thank Nick for this add request. I'm 18, soon to be 19 and dx'd in June of 07'. Here's my story if anyone's interested. Hopin' to meet many more with MS!
Hey guys! I'm not on Tysabri, but a friend of mine started on Tysabri after being on Betaseron for a while, and she feels she's doing a lot better. She really liked the change. If any of you are interested in getting more info from her, I'm sure she won't mind me sharing her email with you. Just let me know. Hope everyone is doing well! Hope you feel better soon, Nick!
i dont kno if i would say deal with the shots..just have to have the mind set that i have to do it and that it is for my betterment. if a small needle sting and maybe a bruise will keep me from a wheel chair then hey...give me the shot. HEY my DR. is talkin bout me goin on Tysabri..ne one on it? what ya think?
hey guys and gals! i went to my neurologist today... kinda depressing... i was old i would probly never see outta my left eye again... but with the novantrone treatments, i'm not having any relapses.. so its a good thing.. but still bad.. i just want to be a normal adult and see out of both eyes. but that will probly never happen again.. also, im not on copaxone anymore... its made me WAY too sick... so im done with it.. just an update on my life.. how's everyone else doing?
My name is Monique and I am from Australia. I happened to come across this profile and found it to be a great supoort network.
I am 18 and I was diagnosed with MS when I was 14. I know that in America Pediatric and Teen MS is not unheard of, where as in Australia the numbers are not very high. I was one of the youngest females in my state to have been diagnosed with MS.
I hope to hear many stories of others experiences and form new friendships.
aww... nicole i wish i could say i was, but im not... i took my shot the other night, and i had a reaction to it... like my chest got tight and my heart started racing... the bad thing is my chest is still tight-3 days later... i miss everyone SOOOO much! im kinda goin nuts without everyone... 4 days with you guys and im still not back to normal!
this page is awesome!! i will definitely send you an email with my picture as soon as i can and anything else i can do to help out with this let me know!!
Now that we have a group of ppl on here I would like to say welcome...lol. use this site to your advantage! leave comments questions and ne thing else on here either for all to see or msg so only one will see. Any questions will be answered! ENJOY!
