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Was nice to see today fishing on the river with my wheelchair. An accessible toilet riverside what.

Paved the way for accessibility.

This week we're spotlighting an amazing blog from Evie that explores the struggle of "not being disabled enough". This is an absolute must-read. Click below to read the blog by @Evie_Meldrum ⬇️ https://shift.ms/blogs/do-i-really-need-accessible

https://www.matchinghouses.com/1-bedroom-flat-london-united-kingdom-0 Perfect location for London, have a look, PM for deets.

I've just managed to book myself a ticket to see Dylan in Hull in October because / and for the first time ever ..... I booked to sit in the accessible seating bit (based on the fact I have a parking permit, a bus pass and PIP mobility payments and obs a SPMS diagnosis) but I still felt a bit 'she...

Hi all, just after some ideas about how people cope with getting in & out of cars & driving. I’ve PPMS & struggle to bend my left leg. I know my MS is progressive but at the moment I have a medical driving license & I’m still driving an unadapted car. I have an automatic Ford grand cmax which at the...

Just stumbled across a link to this on another site and thought it was worth a share here... it's a handbook/guide to accessible days out around Britain. Not had chance to look at it in any detail but might be useful... http://www.accessibleguide.co.uk/downloads/Accessible_Britain_Book.pdf

Morning all. No idea if there are any keen green-fingers amongst us but came across this site for a charity called Thrive who aim to help people with disabilities start or continue gardening and thought it was worth a share. http://www.carryongardening.org.uk/default.aspx

I meet so many people saying "I wish I'd found this place 10 years ago" or "when I was younger". I don't have MS but work with many people who do and after visiting conferences about "cures for MS" and "treatment", I thought what about quality, enjoyable experiences while they look for cures?

Okay apologies for the dump but I just need to yell into the void for a sec… I first experienced symptoms in 2017 and was eventually diagnosed in 2022. My symptoms have got much worse in the last year or so, the fatigue and pain is unbearable most days. I don’t receive any support from my consultant...