#powerchair - Shift.ms

10 Feb 2023 01:55 Edited

Traveling with a power chair

any tips on navigating the process of flying with a power chair? Thanks for any help #powerchair #traveling #flying

15 May 2025 18:10

I was diagnosed in 1993 but knowing I had ms for 10 years before, I now live with my care in a bungalow in louth Lincolnshire, I am in.my power chair 20 hrs a day with the pain and spasticity ,but we are still fighting

Wieliczka, Poland

@Uniquelh

18 Apr 2023 18:33Last reply 18 Apr 2023 18:48

What to do what I do

Everyone is encouraging me to try and keep walking but I’ve just been ordered a super power chair. How do you balance maintaining walking with access to something that makes everything easier?

1

@cazzy

26 Mar 2023 23:24

hi everyone i’m new here.

so i was diagnosed in july of 21. i have secondary progressive ms. due to many previous broken bones etc. it was determined that i wouldn’t walk again. they set me up with a power chair. then last year i was moving from maine to alabama and just as we got to our destination the woman in front of us...

Marietta, United States

@cazzy

26 Mar 2023 23:24

hi everyone i’m new here.

so i was diagnosed in july of 21. i have secondary progressive ms. due to many previous broken bones etc. it was determined that i wouldn’t walk again. they set me up with a power chair. then last year i was moving from maine to alabama and just as we got to our destination the woman in front of us...

Marietta, United States

Unpublished

@Garry_Watton

29 Jan 2023 12:49Last reply 29 Jan 2023 16:56

Calling for help

Hi all, My last post was taken down. I guess it was seen as me being greedy and not being genuine. Here are the facts. 1. I have Primary Progressive Multiple Sclerosis and was diagnosed in Novemeber 2018. 2. The progression has been very fast and seems to be agressive. 3. I ive on my own, I h...

8

Unpublished

@Garry_Watton

28 Jan 2023 14:28Last reply 29 Jan 2023 02:41

Calling for Help

Hi there, I'd really appreciate it if you could share or donate to this GoFundMe, Drive Carbon Fibre Airfold Powerchair https://gofund.me/8cd4a379

9

@Keira74

16 Nov 2022 13:59Last reply 16 Nov 2022 14:37

Hello …

… I was diagnosed April 2008 with RRMS, then December 2012 I was told it was SPMS. I’ve not worked since 2008. Have quite a lot of health conditions now. I’m spending time studying criminology & forensic psychology. It’s keeping my brain active at least. 99% of the time I’m using my powerchair named...

1

@SJL222

28 Jul 2019 13:27

Advice ?

Any advice on how to combat contractions? My legs are contracted and I am mostly using a power chair. Anyone have any additional advice on additional funding sources for paying for at home caretaker other than Medicaid? Thank you, Sheila Lemus

@jkerr

26 Jan 2018 22:42Last reply 27 Jan 2018 09:46

Clonus-type muscle spasm of main skeleta

Looking for answers. I get Clonus-type muscle tremors of main muscle groups such as abs, pecs, gluts, Specialist never heard of it other than hands and feet. They last about 15 seconds and I get one or two a day starting about a month ago. Have had MS 46 years, in powerchair 10-12 hours a day. ...

1

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