Hi im having so much pain its literally like i cant get enough rest (even though i do) internal aches im so confused why my health has declined so quickly..i cant walk far at all without having spine aches severe foot burns the list goes on and i have to sit.. a 10th of what i used to walk some days...

Hello fellow warriors I hope this message finds you well. I know each person‘s battle is frustrating and difficult. Just know that you’re not alone and there are plenty of us out here willing to allow you to lean on them to help boost you up and get you through this fight . I’ve been on this app fo...

Hi all 👋 Bit of a pathetic post, I'm sorry, but I need this. Would anyone be willing to be a friend? Since my symptoms really started getting bad around 18m ago, my mood has just been getting worse and worse and now I just don't know what to do. I have a husband, I have my daughter. They are wonder...

Hi all, I’m in England (I know other countries it seems to work a little differently, that’s what I’ve picked up on this app anyway) I’m curious to know your thoughts. I received a letter today from my MS nurse that states my bloods were done in preparation for ‘potential treatment’ does this mean ...

Hi all you lovelies! So I am leaving my current job and looking for new but what I’m worried about is going back to full time hours and the worry over my health. I currently work 4 days per week. And I know companies aren’t supposed to discriminate against health problems but they do and will and us...

Am praying 🙏🏽 that gives me the strength to now raise my grand daughter and deal with this MS .. how many are raising children and have this health condition

Power yoga 🧘‍♀️ this morning Followed by Pilates then Aqua Pilates- jacuzzi 🥰

Just wondering how many of you have a family history of Multiple Sclerosis like we do in my family. My big sister was first diagnosed with MS, then myself in 2011, followed by my big brother in 2021. Sadly we all watched the disease take my Mum in 2023 which was utterly terrifying. My twin has Lupus...

I knew that something like 80% of Masers had urinary and bowel issues at some point, but I’ve had my disease for so long and not had issues that I thought it wasn’t affecting me, or wouldn’t for a while. Part of this recent flare though has been a combo of retention and incontinence, so has been ent...