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Patients Multiple sclerosis
Spascity and MS
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Tymothy
@Sk8rGirl Hello,
My cousin experienced this and if I remmeber correctly they were doing a lot of physiotherapy...do you do any of that currently?
Sorry ot hear that you are going through... :(
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Tymothy
Sk8rGirl
Good advisor
Thanks so much. I am not having that therapy. I’ll look into it.
Unregistered member
I wish you all the best for a answer to your problem, I was in the Army for 23years and now use a wheelchair more than I want to, but I'm able to out and still have a good day.
JosephineO
Community managerGood advisor
Do any other suffer from spasticity because of their MS?
@kathy52 @Joanne75 @Magda47 @aprilanne @Lindaf @scooby @fionaobrie68 @NatRyan @waltwhite @Vleacy @Daisy30 @nanniesue55 @Kazog61 @bridian @amitch72
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Sk8rGirl
Good advisor
i a new to this site and posted this in the wrong place. My apologies. I live in the US and have severe spascity. I have Botox shots every 3months. It relieves the pain but doesn’t touch the spascity. Do you know if anything else? I’m almost bedridden because of it. I was a professional figure skater so I’m strong except for this.
Thank you so much