Bio: I'm Jane, I was diagnosed with RRMS in 2016 but am determined to not let it define me. Strength, fitness and energy here I come (🤞)

Bio: Diagnosed nearly 30 years ago. Have deteriorated quickly in the past 5 years so need to stop the slide.

Bio: I'm a 44 yr old woman diagnosed with relapsing/remitting MS back in 2008. My life hasn't exactly been easy but I still get up every day and fight

Bio:      Hi my name is Joel, I was diagnoised in 2014 with RRMS. Since I have joined this community it has improved my life drastically for the better!

Bio: Hi, my name is Daphne. I am from The Netherlands. Diagnosed with MS in 2017. I like traveling, love the sun and I have my own business as a homebaker

Bio: My name's Debbie. Diagnosed with RRMS in January 2025 after 4 years of exploration of symptoms. A Group Fitness Instructor and keen gardener!

Bio: T1 diabetic for 41yrs, RRMS for 14yrs with foot drop, fatigue, etc. FES user/fanatic. Keen cook, fan of cacti and gin, just not at the same time.

Bio: Diagnosed with PPMS Fall of 2024 - still working to grasp it all, thankful I found this group. @megsytakesahike on Instagram

Bio: Hi I'm Wendy, 56yrs old Dx rrms 1998, spms approx 2010. Ex riding coach, cat behaviourist. Lost a bit of motivation recently, so happy to be here

Bio: I'm Donna, I've had relapsing remitting MS for 20 years offically but it took ages to diagnose.

Bio: Diagnosed 1 year ago, navigating my way through this slowly, lots of questions but frightened of the answers.

Bio: I used to be a triathlete, and before that, I was an avid runner. mental health issues, weight, disabilities = couch potato for me. Hope this helps!

Bio: New on here just in the middle of selling and buying a flat so will get back to this in detail later!

Bio: Hi Looking forward to start this new journey, I’m 44 years old and was diagnosed with MS in 2012, hoping to improve

Bio: Dx 2004 Love I found this group. Helps keep us going for real. I live alone mostly. Also now epileptic!! Pills now managed. Last one was 10th March.

Bio: Hi. I'm 54 and I have had MS since 1997. My formal diagnosis was in 2002. I have 2 grown boys but no grandchildren. 😁

Bio: MS pp since 2020. Been with Dom since the beginning. Love him to bits. Not very good at the exercise but note to self “I will do it very soon” 😜

Bio: Mum of 2 with MS. Looking forward to pushing myself to feel and be stronger for my kiddos and myself.

Bio: Have SPMS and am keen to max out what I have so am currently a neuroscience student and trainee counsellor. I have flown a small aircraft!

Bio: I am 59 and have had RRMS since 1999.

Bio: Fighting to get fit

Bio: Hi I am looking forward to joining all of you. Diagnosed 18mths age 57 RRMS. Had to stop working NHS after 38yrs. 3 beautiful Grandaughters. 😍

Bio: Hi, I was diagnosed with MS in 1991. I live near Cambridge, UK I love being a Nanny to my granddaughter, I enjoy camping in my motorhome 😊x

Bio: One of my dogs would be my normal profile pic! Doing my best to be a better version of me.

Bio: An ex HR Manager who loves life with my Husband and our 7 year old daughter. Only problem is flipping MS! !

Bio: Had MS symptoms in 2003 and diagnosed in 2004. It’s bloody 💩but I’m still laughing and moving 😊

Bio: Guitar teacher focusing on improving my health and fitness. Passionate about family, music, Martial Arts, science, maths & computing.

Bio: Had MS for a long time. Never really liked excercise but doing the MS Warrior Programme has been a real eye opener with me now enjoying exercising.

Bio: I was diagnosed with MS in 2015. I am a firm believer that diet, exercise and positive attitude makes a big difference.

Bio: Hi I'm Jo, mser for 11 years, rrms. Mum of 2 retired nurse. I enjoy going to the gym, reading and knitting