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Patients Multiple sclerosis

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Posted on

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

Beginning of the discussion - 24/01/2019

Spascity and MS


Posted on

@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... :(

Spascity and MS


Posted on

Thanks so much.  I am not having that therapy. I’ll look into it. 

    

Spascity and MS


Posted on

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.

Spascity and MS

• Community manager
Posted on

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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