Hi everybody,
I was diagnosed with PSMS two years now. A month before the first lockdown. So you can imagine no real support available for me. I used to be a strong independent person with a sense of humour . Now I’ve got no friends who call to meet for a coffee. I feel so isolated. I don’t like tra...
Hi everyone, I was diagnosed with RRMS about 2 years ago (only just found this site through the BBC article, which I am very grateful for) when I was 19, in my first year of university.
Symptoms have not affected me too much (my main problem being fatigue and leg numbness) physically, I am strugg...
“My neurologist said, you've got MS. I remember walking out of the appointment and just sort of, not believing it.” 💚
This week's episode is with the inspiring @Sarahemily who reveals what it was like to have her confidence knocked by MS.
Has MS knocked your confidence at all? Share your story i...
“Finding a new purpose by getting to help people who are new to MS has built my confidence. I get to connect with people who need somebody.” 💚
This week's episode is with the fabulous @M_S_Positive who shares how MS impacted her physical appearance and confidence. If you’ve ever felt this, it’s a...
I really struggle with drop foot and balance. I hate it and really impacts on my confidence at going out.
However, I recently discovered Barefoot shoes and have definitely helped with walking and feeling the ground.
I still use a walking stick and/or walker but feel more confident now.
@Confidently__chronic (two underscores)
I created this instagram page following a very tough time with MS & work issues I faced following diagnosis which made me lose all confidence.
I created this page in the hopes to bring everyone a sense of positivity with our diagnosis. 🤍
& a reminder that we...
Hi everyone 👋
I’m Eilis, a postgraduate psychology student from Ireland and a fellow MSer. I’m currently running a study exploring how coaching might support people with MS at work — especially in areas like resilience, confidence, and navigating disclosure.
If you’re 18+, living with MS, and curre...