Thanks for the replies, nice to know you aren't alone. I'm so new to all of this, very strange! I try not to let it control my life but I've just heard about...
I wasn't OFFICIALLY diagnosed for almost twenty years...because I wouldn't go back to a neuro after the first one gave me a mylogram (sp?). In that twenty...
From what I have read there is no actual test for MS, the lesions don't always show up. It's primarily a diagnosis based on exclusion. Have you been to...
AN IMPORTANT ANNOUNCEMENT THAT MAY BE OF INTEREST Brief Survey for Teens with Multiple Sclerosis A leading pharmaceutical company in the treatment of multiple ...
Hi everyone, I joined this list hoping to get some opinions about my symptoms. I know you can't give medical advice so I am just hoping to find out if this...
Welcome to the list. In regard to your symptoms...have you had any tests done yet? I would ask the doctor to order an Xray and or a MRI of your cervical spine....
Please, if you haven't seen your doctor about this numbness and tingling in your lips, thumbs and tongue, do so at once. Please do not ignore. it. We all care....
They probably told Becca MS because it comes and goes, could be many things tho. Could even be an allergy to something. (I'm allergic to Zitrhomax - an...
NEW AIRLINE SECURITY-PRESERVING RIGHTS OF PEOPLE WITH DISABILITIES In securing the U.S. air transportation system, steps have been taken by the Department of...
Hi everyone. My name is Amy. I joined this group because about 3 years ago I was diagnosed with RA, but have recently begun to have symptoms of MS. I realize...
IS MS HEREDITARY? There's new evidence to support the notion that multiple sclerosis is hereditary. Researchers used a powerful imaging device to examine the ...
Hi, If anyone would like to purchase an Invacare Patient Lift 9805, I have one for sale. Unfortunately I cannot ship it because it would cost too much money,...
Hi there - I'm new to the group. I joined this particular group because it said something about being uplifting and I certainly embrace that approach and look...
Hi, Welcome to the group. I'm rather new to this list too and I have noticed it's a pretty quiet list compared to some of them I'm on. But hey, I welcome you...
Hello Group, As I have told you before I was diagnosed with MS a little over three years ago ,I have been up and down with this ,everyday seems to bring a new...
MKandMK
Oct 12, 2003 8:44 pm
3718
Hi, I'm Zoli from Budapest, Hungary (SM diagnosed in '98, age 32, single, living with my parents, pensioner - this was the introduction, you can see me at my ...
I hope Michelle can find a local ms support group and social services. This is the time to ask for help. You can get better. This disease can have its ups and...
I did read somewhere that migraines and normal headaches are common with MS patients. I get occasional headaches but my brother, who may also have MS gets...
Tali wrote: I did read somewhere that migraines and normal headaches are common with MS patients. I get occasional headaches but my brother, who may also have...
I was diagnosed with MS two years ago. I hate the memory loss, headaches and fatigue more than my friends think I do. I have discovered that taking Ginkgo...
, I'm glad Zoli is joining in and posting. Your English is pretty good too! You may see that I posted before about headaches. I think that you should have your...
What have the doctors said tp you Marilyn? I take it you have normal cardiac function? Does the Lasix help with the swelling? How much activity are you able to...
Hi..this is Granny Red. This is something that is embarrassing to talk about. I can rarely go anywhere because I have no real control over my bowels. This has...
I have heard that stuff like St. John's Wart and the like are NOT things people with MS should take, as they play with the immune system, and most of us have...
Granny Red, I too have the bowel/bladder problems. Bowel is my biggest problem. Changed my diet, didn't work, had all the tests done, show nothing. (This was...
HELLO EVERYONE HERE! ;O) I guess that most of all "patients" :)) with MS, do have or did have the same problems with bowel and Bladder also. Maybe it can be...
I just can't seem to stop crying. I'm emotional for no good reason. Does this happen to anyone else? Maybe I'm just over tired. I didn't sleep much last night....
If you come up with anything, let me know. My system is sluggish, due to MS, and drives me nuts. I am on Polyehtylene Glycol (Miralax) and Tegaserod ...
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