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Real members of MyMSTeam have posted questions and answers that support our community guidelines, and should not be taken as medical advice. Looking for the latest medically reviewed content by doctors and experts? Visit our resource section.
A MyMSTeam Member asked a question 💭
Edmond, OK

I have only been diagnosed with MS for a year and a half. Never had any real symptoms until my right leg was getting weak. I walk fine if I take it slow but when I get tired my right foot tends to drop. Both of my neurologists told me that many people with MS do not end up in a wheel chair now because of the medications that slow down the progression. I have done my own research and know what they said is true but I'm curious how many people on this site walk without assistance or use a… read more

September 21, 2013
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A MyMSTeam Member

I walked terrible when I was diagnosed in 06. Now I am running. I took a natural approad with diet, exercise and vitamins. It took a ling time many meltdowns from depression but I was able to do it. I would not give up.

September 22, 2013
A MyMSTeam Member

I've had the MonSter living in my body for well over 25 years, possibly longer.

Fatigue is a major factor in whether I use assistance or not. I may go from walking reasonably well to walking like a drunken sailor within a few minutes. I always take at least a cane with me when I am out in public, even if I don't need it when I leave the house. I'd rather not be seen as drunk and disorderly...LOL Besides, lots of doors are opened for me when I have my cane, or walker, or whatever.

I tried Avonex and Copaxone and had bad reactions to both. I currently only take Zocor (simvastatin) for the MS. It works for me.

September 22, 2013
A MyMSTeam Member

I walk unassisted. I was dxed Oct. 13, 2009. But by the 30th I could not walk. I had my first known relapse and it was very hard. I started PT on Christmas Eve and walking even since. The first year after the relapse was very tough. But I am so much stronger now.

September 28, 2013
A MyMSTeam Member

i use walls i know them by name around the house

September 26, 2013
A MyMSTeam Member

I was dx with relapsing/remitting in 1997, used a cane a couple of years later, then a walker. In 2003 I no longer had relapses and was considered secondary progressive & began using a power chair. My MS specialist told me I have a "bad" case :(. On the positive side, using the power chair conserves my energy and allows me to do more. I'm still able to drive and for the most part, don't let the chair stop me from doing what I want to do.

September 24, 2013

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