Anyone deal with mood changes. I seem to have several days or longer that I feel great and full of energy and positivity then I seem to get depressed a little and then usually really irritable and emotional. Its like the sky is falling g ove night. I dont want to take meds like antidepressants bit ...

Hey. I am working with a practioner who suggested making friends with other MSers with either bowel or bladder urgencies (I seem to have both). Sharing stories. Normalise the topic. Understanding each other. And so on. Anyone?

Dr. Ewa Dabrowska's (from Poland)diet deacidifies the body and offers antioxidant properties. The menu includes raw vegetables and fruits, salads, green smoothies, soups, pickled vegetables, and large amounts of water with lemon. Person with MS improved after diet.

Heya, I just did a 90 minute Microsoft Teams interview with a Researcher at Marquette University about my perimenopause experience last night. *I'm guessing this is only for US residents* Her team is interviewing women to get details of on the ground data to see how if affects those with conditions...

According to this news article: https://www.independent.co.uk/life-style/health-and-families/health-news/fampridine-multiple-sclerosis-ms-treatment-nhs-b3020019.html?fbclid=IwVERDUATPPmhleHRuA2FlbQIxMABzcnRjBmFwcF9pZAwzNTA2ODU1MzE3MjgAAR6hAjKqktIGn9eTgGcwQb4L1JzfcRndijEQ2mHaxC8jg90DOfDt9cpr54m6Ug_ae...

Probably the sunny weather but my hair keeps on falling out does anyone else the same?

July 2026 marked the completion of the first year of my initial treatment cycle with Mavenclad. Prior to this, I had been treated with Fingolimod for several years, but last year I was hospitalised twice with severe UTIs. At the time, I was significantly immunocompromised. Initially, my dose was red...

I started on glatopa when i first got diagnosed with only one lesion on the right side of my brain. Six months later, i had a relapse and was told i had another lesion on the left side of me brain, which is rare they said. They put me on tecfifeta. I was on that for 5 years. The last MRI i has said ...

This is my worst MS Symptom. I have tried Intermittent Self Catheterisation. For me this did not work. A few minutes after emptying my bladder with catheter I need to pass urine again. In the end I was admitted to Resus with Urosepsis. So stopped ISC. Have rescue dose of antibiotics when I get UTI. ...