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Hi all, This is my first post on here. I'm newly diagnosed (a few months) and have been taking some time to try and get my head around it all. As part of this, I've thrown myself into research and have found two things that have really helped me: (1) a number of population studies showing, on the...

Hi all,new on here. Been diagnosed 3 1/2 years. Just started Kesimpta after being on Ocrevus. So far so good! Just wanna say that on Sunday I completed my first race of the year! 8 miles coastal path challenge with 1,400 feet elevation. Over the moon with my time. Living in West Wales hills and elev...

What ever we are going through with the illness and with other issues going on around us. Let us remain upbeat and positive. Indeed, that is my message for today. It's tough, it's very tough. I try, I do try to smile through it.

Live for today. Tomarrow is a gift not promised. Find the good no matter how bad. I say no cause no cure why the pricy meds? They say they help with relapses. Hmm okay. Well, I have been on my fav copaxone for over 14years. I don't do rebif it was suicidal Tecfidera made me rudolf the rein...

Hi Everybody. I have been diagnosed and been living with MS since 2010. Don't get me wrong it has not been easy living with this condition but then again i have been living type 1 diabeties for 18 years and that has not beaten me and that goes for MS. Don't get me wrong i have my good days and my ba...

Seem to be posting a lot recently but it’s on my brain.. has anyone got any positive stories of living with ms? Everything is so doom and gloom has anyone had the condition say for 20 years with little progression? I think everyone needs some positivity

Hey all! Just wanted to say a big thank you for the past few days, it has meant so much to me knowing that I'm not completely mad in my thought process!!!! Had appt with Neuro and will be switching to Lemtrada....that's a whole other post! But managed to actually tell my hubby what I was feeling a...

Hi everyone, I know that it just isn't possible to stay positive all the time in the face of MS, and we shouldn't be expected to, sometimes it's tough and we just need to let ourselves feel how we do in that moment. BUT I would really love it if from time to time we could all share something that w...

This week we're highlighting an awesome blog from @jennifer exploring toxic positivity around MS. Have you ever felt pressured to downplay how hard MS can be? Click below to read the blog by @jennifer ⬇️ https://shift.ms/blogs/when-positivity-becomes-toxic

Since being diagnosed with MS in August 2021, which was 1 month before starting my final year at college (year 13), I had nearly lost all hope in my future and the goals I always wanted to achieve. I would always ask myself why now? A few weeks before starting the year with all its ups downs. Went ...