One of the first symptoms I ever had was numbness in my legs. Often it felt
like the veins in my upper legs were getting ready to burst. Very painful. Then
the numbness. Don't let your doctor ignore it. Every one of the male doctors I
had just looked at me like I was a complainer. The numbness would really come on
when I was out walking. I got rid of my pride ( old people like me have a hard
time with that..:>) ..) and now I use a cane for very short distances and a
big fat wheeled walker with a seat on it that is a blessing when my legs have
completely given out. After a little rest, I can go on.
I will tell you what I told my grandson who had a terrific heart disturbance and
was in hospital for a week. Keep saying to yourself..."Every cell in my body IS
healthy and strong". Do not say they WILL be healthy and strong.....say IS....as
of right now. You may not notice an immediate change, but keep at it. Every day.
Write it down somewhere so that you will keep noticing. Stick it on the face of
your computer or TV or near the shower, whatever you are near.
My grandson is home and doing great, and of course taking all his meds as
prescribed. He is 42...had open heart surgery at age 4. When he went into
hospital last week, his pulse was 150 and his blood pressure very low...we
almost lost him.
Anyway, please try this. You won't have any side effects and certainly no upset
stomach!!! I know this is what helps me to keep going so I can do my own
housework and shopping, etc. Sure I still have aches and pains, but not nearly
so severe as they were...the kind that really shot me out of the sky, so much so
that at times I couldn't raise my arms to get my clothes on. Real bummer times.
May the Great Creator bless you and keep you safe and strong.
Love, Granny Red. (great-great!! )
Hey, everybody..I'm still in there swinging!!!
Your condition might be due to many things but it is very wise to start by seeing your GP who may well refer you to a neurologist. I was 48 when my MS...
One of the first symptoms I ever had was numbness in my legs. Often it felt like the veins in my upper legs were getting ready to burst. Very painful. Then...
The symptoms can be explained by other things besides MS - the hand and arm tingling could be carpal tunnel syndrome and the tingling in your legs after...
stowne517
Apr 8, 2005 5:15 pm
For quite awhile I have noticed, intermittently, that I get pins and needles, especially if I bend my arm back, (as if I were scratching my back). It was only...
I am 27 and a mother of one. I have had a few automobile accidents. Most recently, was a year ago, I was hit in the back of the head with a log.(don't ask) For...
I am new to this chatroom and was diagnosed July 1, 2004. Since my diagnosis, I haven't done much as far as drugs. I would love to know any natural meds anyone...
I understand how you feel, I was diagnosed in September of last year and since I have multiple family members with the disease, Everyone has been through...
Yes, yes, yes. You will get people wanting to explain away your symptoms. The most common I have found is "Well I (or someone else) have that symptom and it...
I suggest that you don't hold off on starting treatment!! The current standard of care in MS suggests that you should be on one of these drugs ASAP. This is...
Hi there, I've had MS since 1989 and was on Beteaseron when it came out, also was in trials. When I moved to VA the Doc put me on Copanoxe, but last week the...
Hello, Another new member! Was given diagnosis 4-25-2005. Optic neuritis back in Dec. 2004, 3 MRI's later, have 1 active lesion on spine & 1 active on brain....
Hi Lou ~ I was diagnosed in 1989 as well. Progression was slow for the first several years but I tried Avonex for a year. I didn't respond to it very well. Had...
I don't usually post here, but I do read these posts. I've been holding off doing the shots for 9 years and I still get around albiet with a cane. According...
bubbina_1999
May 8, 2005 3:40 pm
I met a lady who is going through chemo treatment for MS not for cancer. She's happy about it but I personally wouldn't want it. You can ask your Doctor if you...
Hello, Every therapy is good for different patients. I think that interferon based meds have more side effects linked to them. But if it works for you its...
I just read in the MS support group that only a 1/3 of MS patients respond to A-B-C drugs so I think treating the underlying problems is more important then...
I completely understand your skepticism about drugs; with them, the entire concern is about money! However, I have to say that my personal experience has to...
I was wondering if we would all be willing to say what drugs we are taking at this time & why that choice was made. At the moment, I'm on once-a-week beta...
I have had medical problems for the past 4 1/2 years. Much of it relating to the spine and brain. I had cervical anterior diskectomy surgery with plating 2...
nyboy1960 wrote that he read that only a 1/3 of MS patients respond to A-B-C drugs. I don't think this is right; do you have a source? There has been a lot of...
All of the information I have read as well showed a 1/3 reduction in exasterbations as well. I would also like to know that persons source of information....
The only thing I would add to the ABCs reducing exacerbations by about 1/3 is that this is an average. Some will do better, some less than the 1/3 reduction....
Hi all, In response to the statement that only one third of MSers respond to the ABC drugs: I agree with Howard. Someone misread the info from the data....
Msjnich
May 16, 2005 12:01 pm
I agree, it does depend on the individual. I have tried all of the meds (Avone, Betaseron & Copaxone) and none of those worked for me. I've been on Rebif for 2...