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Hi all, has anybody managed to get a disabled person's railcard lately? (Who does not qualify for PIP) If so would you mind sharing the process and what was needed. TIA

MS has isolated me from the rest of the world. Lack confidence to search for love for fear of rejection. Just wondering if there is any site for disable like me to find love. OR should we start here a dating site even if it is virtual dating. It is just a question I am asking. sorry if it is no...

I thought I knew #ChronicPain ( and I don't mean being unable to score some sticky Icky) Then, during a month long attack of #sciatica (not my first) I developed a fucked ankle (not a medical term) - presumably #MS #spasticity in the peroneal muscle (shin/calf - not per_I_neal!). Can't walk (got t...

This is the second relapse I've had this year thats been really disabling. Loss of power in both legs, weakness, and foot drop. Double vision in my peripheral that hasn't recovered from the last relapse 6 months ago. I competed both years of Mavenclad and was in remission last year. Up coming MRI ...

Great article from Gavin Giannoni on this topic. Applies to Kesimpta and rituximab as well. If you have Substack, you can read for free. https://open.substack.com/pub/gavingiovannoni/p/serious-infections-on-anti-cd20-therapies?r=2f3ys&utm_medium=ios Bottom line - there is a 7% risk of serious infe...

Hi, everyone. In the past, I've managed to navigate airports on my own a couple of times, but I've not flown outside the UK since 2018. I was diagnosed with MS during the pandemic and began socialising far less than I used to and done it closer to home. I am now itching to travel abroad on my own...

Hello, I’m new here😃 I’m Callan and Im from Scotland. I have suffered with health issues mainly chronic pain since I was 15/16 years old. I was told I had fibromyalgia even when my symptoms worsened and I got more new bizarre symptoms I was reassured it was fibromyalgia and told to ‘stop searching...

I've been watching videos on YouTube about people being questioned by other disabled blue badge holders on whether they should be parking in disabled car spots because "they don't look disabled". I think it's disgusting. If anyone said that to me, they'd get their answer. I have to admit. When I par...

I barely leave the house since diagnosed in June.. I have relapsed since then.. causing both my legs to be numb, including perianal areas. I cannot even just sit or lay down without being in pain.. so standing / walking even around my house is very difficult.. I have a holiday booked very soon which...

Hi everyone im new here and fairly new to RRMS. I had mt 1st visable relapse march 2023 doc told me i jad meningitus (wrongly diagnosed) then in october i was in hospital for a week after a number of scans and lumber punctures i was finally diagnosd in feb with RRMS ive been on 100mg a day of anatry...