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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

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?

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...

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...

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

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...

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

… 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...

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

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. ...