I wonder if anyone has any advice/tips? I’m 53. I have RRMS going on 10 years. I’m in a wheelchair and my right side doesn’t work. I feel the thing that affects me most- worse than the wheelchair is my bladder. Today by midday I have had to pee 8 times. Hailing myself off and on toilets has knackere...

I’m trying to find hobbies that require little energy and can be done sitting and such. I enjoy painting but do any of you have suggestions? Thank you!

What things annoy you the most? With your Ms Mine is chewing loudly, untidiness, stupid annoying moaning sounds, annoying people..!!!

​Situation Summary: Since 2023, fear and anxiety led you to conceal symptoms and request alternative diagnoses from doctors to avoid an MS diagnosis. However, brain and spine MRI scans ordered by your neurologist ultimately confirmed Multiple Sclerosis. ​Key Points: ​Natural Response: Trying to avoi...

shift.ms was a great help and a lifeline when i first got diagnosed with RRMS in 2022. jump 4 years, to the month, forward: i now have SPMS i now have frontotemporal dementia i am now 50% paralysed i had an IQ of 154, now i can hardly keep my cool or string a sentence together. i was a successf...

Morning everyone 👋 I have ADHD combined and relapsing remitting MS. I can have hyperfocus or be very hyperactive with my ADHD and then burnout and suffer seriously bad fatigue from my MS. Does anyone have a similar experience and some tips on how you balance the two?

Hey yall - I wanted to ask if any of you can relate. I have been admitted to the hospital in my town 4 times in 6 months - all the times are for sepsis and it truly scares me. I have lost 30lbs I didn’t intentionally do, so of course my doctors are concerned. Anyone have any thoughts on things I ...