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I tried to draw some sketches to describe how my MS felt to me and people thought I was depressed. I'm really not. I just wanted to show how badly the sickness gets sometimes. Soon after, I stopped drawing about the negative impact of my MS and started making a fairytale out story out of it. 💪🔥

Hi All, I am new to this site and wanted to introduce myself. I was unofficially diagnosed with MS whilst living in the US but due to limited understanding and MRI facilities in the UK, not officially diagnosed until 2008. Currently medically retired and enjoying life. I have spent the lockdown peri...

At present I'm fortunate to have a parking space at my office. However post covid my team will be doing a mixture of home /office work. Unfortunately the new office doesn't have parking on site and I'm honestly not up to a long walk and two bus journeys. I've decided to try and apply for a blue badg...

Hi everyone, is there financial help towards work involved in widening doorways when that’s needed for wheelchair access? I’ve PPMS and starting to prepare for when I move my bedroom downstairs. Having a wetroom fitted & a new kitchen so thought while building work being done & house ‘up the...

Hello all, I'd like some thoughts from you knowledgable folk plz. I was diagnosed rrms in September 2017 and have been on tec since March 2019. I have remained stable, however my most recent MRI last month (delayed from March) has shown 4 new areas of inflammation. I have not had a noticable relap...

https://www.youtube.com/watch?v=mzaidLfVgSY&feature=youtu.be The world 🌍 of health is adapting to an entirely new way of operating, including switching to digital delivery of care and telemedicine. But what does this mean practically for people with MS? 🤔💭 In episode 1 of this miniseries, we’re ...

Hello all, I'd like some thoughts from you knowledgable folk plz. I was diagnosed rrms in September 2017 and have been on tec since March 2019. I have remained stable, however my most recent MRI last month (delayed from March) has shown 4 new areas of inflammation. I have not had a noticable relap...

Hello all, I'd like some thoughts from you knowledgable folk plz. I was diagnosed rrms in September 2017 and have been on tec since March 2019. I have remained stable, however my most recent MRI last month (delayed from March) has shown 4 new areas of inflammation. I have not had a noticable relap...

started one month ago and having some stomach/digestive issues. Posted list of side effects says this should pass in two weeks. Not my experience and asking others if they’ve experienced anything similar. thanks

Hello everyone. Just wanted to say I thankful for all the new people I have met so far. I like hearing everyone's personal story, and all the great advice. This is truly an informative place with lovely people. Stay safe friends.