Hi! I just had to share this tiny win that made me so happy. I recently got a silicone non-slip mat for the shower and honestly, it’s been amazing. Because of the MS balance issues, I was literally too scared to even close my eyes in the shower anymore. But with this mat, I felt so grounded that I f...

Have anyone ever heard of this step Nura that supposed to help with foot drop muscle weakness they got appetize on social media for managing MS

My son going to school for neuroscience and shadowing with my doctor

Hi shiftms fairies🧚🏻‍♀️ I’m an Electrical Engineering student, and I’ve been diving deep into how sensor technology can help with MS symptoms like balance or walking issues. I’m really curious about what’s happening in the real world outside of my textbooks. If you use any wearables (smartwatches,...

Need help understanding. I was diagnosed with MS 2011, thankfully only relapse twice. When first diagnosed i couldn’t walk for about a year.. now i walk with walker or cane. Lost sensation in my lower extremities. Very scary times. As the years have passed my legs & feet hurt so bad. They hurt, bur...

I’ve had MS officially for 20 months now and started Kesimpta 16 months ago. I got results from my second MRI since starting treatment and pleased to say they noticed no significant changes. I’m very happy about this and proud of myself because although the treatment is a big factor, I believe my he...

Hey everyone. I'm tired of crying everyday .... what is that you do to get you out of the funk ? It's been 8 long years ! I just want me back! THIS IS MY BODY! AT LEAST I THOUGHT

MS did not make you strong. The fact that you decided not to commit suicide with the highest suicide rate & depresion out of all disabilities and chronic illnesses shows you are strong. But it's not even about strength, make life count if you did not already before being diagnosed. Don't justify pai...

Hello my fellow MSers, I thought it would be useful to do a MS patient pack. You know my experience has been the NHS leaving me to die and then bully me. No one bullies me & Londrina! So check this out- Listen you are disabled, you have MS and depression lives with us please deny it BUT you are ...

Where are you joining from while living with Multiple Sclerosis? 🌍