My husband has had MS for at least 24 years and I like reading whatever I can about it - seemingly more than he does. I will most likely just "lurk" unless...
dlsmith
Jun 2, 2007 2:01 pm
4652
Hi! I'm Barbara. I am not yet diagnosed w/MS. I feel like such a hypochondriac. I don't dare go to an M.D. I am seeing a Naturopath. So far, he is failing at...
I am very discouraged right now. I recently had an exacerbation - was taken to emergency room with 105 degree temperature and could not control shaking and...
Loni is entitled to have angry and depressed times! I'm a therapist and also have MS. It may help to write down your angry and depressed thoughts or say them...
I'm not sure if this message will get through but I will try it anyway! If you are feeling down that's ok because everyone feels down sometimes, even people...
Hello everyone! This may be opening a can of worms, but I just wondered if anyone else ever got the feeling that their medicine was hurting more than helping?...
I have had MS for years now, diagnosed officially for 4. I also have bouts of the full body "achiness", its very uncomfortable and painful. My last bout of...
This must be harder because she has MS with Alzheimers any suggestions for coping with this - it's really hard because she is a completely different person now...
Hi there! I'm a new member to this group (and to yahoo, so bare with me). I'm a 23 year old female. I've had MS since June of 2005, so I just celebrated my 2...
I too have had the same thoughts, thoughts that niggled away at me. This is only from experiencing various medications. Avonex was definitely bad for me, as...
You're not a guinea pig! Copaxone has been proven to work in large studies however, there may be people for whom it doesn't work. But if you haven't had any...
Hello, I have a very different experience with Copaxone, but perhaps some other medicine might work better for you. You have to remember also that 50% of you...
HI, I am new to this group, but have been using Copaxone since September of 05. I have had an outbreak of hives once and it was directly related to copaxone....
Thank you everyone for your thoughts, experiences, etc. I had already planned to talk to my doctor, but just wanted to know if anyone else had had the same...
Hi, I have been informed by my neurologist that I may (or may not) have MS. I have had many tests (including several MRIs, a spinal tap and, most recently, a...
Hi, I am among those who have never had a defnitive diagnosis. In a way it's good to have a dx because then you know for sure, but in another way it's good...
Hello My name is Juanita. I was first diagnosed with MS at the age of 15. Currently, I am a 34 year-old mother who recently started to think about the effect...
Hi, First I would like nothing more than to calm your fears. When I first found out I had MS, I was very angry and scared as you are right now. It took me...
Hi - Many of us have gone through the same frustration and uncertainty. Try no to get upset. That will only further aggravate the situation. Always remember...
My condition started the first week of April (this year) when I awoke with one foot slightly numb. I didn't think much of it, thinking I must have slept on it...
It took me 2 years to be diagnosed with symptoms of gait, 1/2 of my body was numb, straight down the middle, fatigue,complete loss of left arm/hand, eye...
Hello, My name is Samantha. I live in Colorado with my husband Todd and 3 great boys, Ty (11), Tanner (8) and Tegan (4). We have a small (40 acre) ranch...
Hi All, Like Jill I have recently been given a "possible MS" diagnoses, just this week. Unlike other folks I've read on here my first major exeacerbation...
Hello all - Over the past few years I've had some symptoms that have me a bit concerned, and I thought I'd see if anyone else came up on MS this way. It...
Hello My name is Dan and I am 43yr. I live here in Georgia and I have a 14yr son who lives with me. I have had MS for 4yrs now. I have been divorced about the...
I have had all of the same things and you are the first I remember hearing of like me. I have had MS for 2.5 years now. I was on every medicine possible for...
I have secondary progressive MS and the neuro claims the pain+fevers I also have is severe Fibromyalgia (every point is painful) but the Rheumatologist says...
mummyratnz
Aug 4, 2007 5:54 pm
4683
Hi there, my name is Terry and I've been dx'd with MS for 2 yrs now so I know what many of you are going through. I was wondering if anyone here has been put...
