Even when you feel at your lowest, never give up. I got down to 107 lbs the last relapse. Messed with my ticker, weight, mood, sleep. I got so weak I could barely carry myself. I silently gave up my work outs and my sanity. Well I’m back to 2 miles a day. Slowly working everything else back in as we...

Im so tired of shit all I want to do is scram and rip people's heads off but I cant I have to pretend everything is ok my stress levels are through the roof and im in the middle of everyone's problems they all bitch to me and treat me like I can't do shit anymore and when I try to do or defend my se...

This weekend was the first time that MS fatigue kept me from something I was really looking forward to doing. I was diagnosed in August 2025 and have been doing fairly well, all things considered. But the perfect storm of my period starting and MS fatigue hitting the same time left me not able to at...

Hi neighbors & community friends 🤍 I wanted to share a quick update and ask for your help. I’m currently developing the HALO™ Assistive Haircare System through my company, INFRAGILIS BEAUTY™. It’s designed to restore independence for individuals who struggle to wash or style their hair due to mul...

Wish me luck. Hitting the neurologist @11 😵‍💫

Hey everyone, I'm finally becoming a member of a gym that I've been going to for a while, and I'm wondering if I should disclose that I have MS. I hide it well–or at least I think I do–but I guess I should for safety reasons. That being said, I'm in-tune enough with my body to know when I'm appro...

I have my first MRI today since I have been diagnosed and started my treatment. 🙈🙈

Whenever I think the shock of being diagnosed is over it’s not!. I still find myself getting teary eyes when I speak about it to people who aren’t aware of my condition and it’s so annoying. I think have come to terms with it and I do feel a lot more comfortable talking to people but I still want ...

Hey everyone, I follow a couple of different MS accounts on Facebook, and I often hear about MS clinics. I live in California and I’ve never been offered a chance to visit a clinic specifically for MS. Is this something that only exists in other countries like Canada and the UK, or do other states/...