Patients Multiple sclerosis
Topic of the discussion
Posted on 22/01/2019 17:16
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 - 24/01/2019Spascity and MS https://www.carenity.co.uk/forum/multiple-sclerosis/living-with-multiple-sclerosis/spascity-and-ms-2689
Posted on 24/01/2019 10:47
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... :(
Posted on 25/01/2019 23:41
Thanks so much. I am not having that therapy. I’ll look into it.
Posted on 01/02/2019 14:55
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.
Posted on 17/04/2019 11:39
Do any other suffer from spasticity because of their MS?
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