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Spascity and MS
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@Jacricrait3115 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... :(
Jacricrait3115
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Jacricrait3115
Last activity on 02/01/2021 at 22:59
Joined in 2019
15 comments posted | 5 in the Living with multiple sclerosis group
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Thanks so much. I am not having that therapy. I’ll look into it.
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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
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JosephineO
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Last activity on 15/07/2024 at 09:21
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989 comments posted | 44 in the Living with multiple sclerosis group
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Do any other suffer from spasticity because of their MS?
@Hoafaynouthus1 @Hidden username @Hidden username @Hidden username @Hidden username @Hidden username @Hidden username @Gloagleeyan7 @Hidden username @Hidden username @Mabaifroar191 @Bloaflet @Hidden username @Hidden username @Hidden username
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Josephine, Community Manager
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Jacricrait3115
Good advisor
Jacricrait3115
Last activity on 02/01/2021 at 22:59
Joined in 2019
15 comments posted | 5 in the Living with multiple sclerosis group
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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