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New here

Hello everyone,

This is my first post here, so please be patient.

My husband was diagnosed with MS 10 years ago after optic neuritis took most of his sight.

He was on Betaseron until about six months ago, when he changed doctors, and was put on copaxone
because he kept having relapses.

Since going on the Copaxone he has lost his appetite, and eats very little. He says food just gags him. He has lost ...
Read more : New here | Views : 537 | Replies : 10


HI Friends researchers of the centre for neuroscience research at children's health system believebto have found what they call a potentially novel therapeutic target. this would not only lessen the rate of deterioration of brain cells caused by MS
Read more ... -study.htm
Read more : RE:PROTEIN MAY REPAIR BRAIN TISSUE DAMAGED BY M.S STYD S | Views : 531 | Replies : 0

New and Med Free

Hi I just jumped on this site today looking for others who are taking the natural path like me. I was diagnosed in 2008. I used Copaxone for a year and a half. Due to numerous side-effects or allergic reactions, I quit. I focus on vegan/raw vegan and gluten free diet. I also do yoga, walk and running. I've been symptom free since I quit meds. I also believe that stress or emotional repression has ...
Read more : New and Med Free | Views : 717 | Replies : 14

Hello everyone

hello everyone, my name is Christopher Barra. I am a 24 year old male (25 in two weeks :-| ) I am brand new to this website and just wanted to introduce myself.
So 5 years ago (20 years old) I had a run in with optic neuritis in my left eye. They could never figure out what it was from. But all my tests for ms ...
Read more : Hello everyone | Views : 1357 | Replies : 21

New to the board

Hi all. New, obviously. I do not have MS but know someone with it. I am here to seek information and advice and learn as much as I can. Thank you!
Read more : New to the board | Views : 393 | Replies : 1

new here but not new to MS

I have had ms since 1998 or thats when they thought I had but no symptoms lol I truly didnt know what was happening doctors finally in 2005 decided I did for sure have it and started me on meds been on a few rebiff ,the infusion and now tecfidera I love tecfidera I love how much better I have been feeling infusion put me in hospital twice so was off any meds for it ...
Read more : new here but not new to MS | Views : 403 | Replies : 0

No mri

No mri

Tue Jan 14, 2014 8:57 am

Hi..I am neg lyme and lupus with many MS symptoms. Buzzing sensation left leg, black hole in vision, burning sensation left neck and back, foggy headed, feel bruised on left arm but no bruising. Neuro said non contrast brain mri was clean so it cannot be MS. Can I have cognitive issues if there are lesions on spine and not brain? He did not seem to ...
Read more : No mri | Views : 724 | Replies : 3

How do I help my husband thru his flares?

My husband was diagnosed with MS 13 years ago after a bout of optic neuritis. He was symptom free for 12 years. Now he has flares whenever he is stressed. His symptoms are mostly neurological. He will become emotional and then seem awake but not able to function. Sometimes he will just sit and it will pass, but other times he seems insistent on finishing whatever he was doing but he is not able to ...
Read more : How do I help my husband thru his flares? | Views : 617 | Replies : 7

New User....Intro

Hello all, I've been dx since 1996, rrms, on Gilenya for a year now. Wanting to know if any of you have had side effects of chills, flu-like symptoms, bad headaches, nausea, extreme tiredness (worse than usual ms fatigue)...if so, what have you done about it? Thanks
Read more : New User....Intro | Views : 444 | Replies : 1

Im new here and have some questions :)

Hi my name is Emma and I just got diagnosed 2 weeks ago. I just started getting a tightness in my knees and im very worried. Does anyone else have this problem?
Thank you
Read more : Im new here and have some questions :) | Views : 563 | Replies : 6


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