Getting Back Into Exercise With Aggressive MS | MS Awareness Week 2018 Day 3 

Just got my diagnosis this week, and right now I'm moving from doom to motivation... keep going!

Love this! My husband is huge on fitness and always tries to get me to go running with him, but I can never keep up and it definitely frustrates him (and me)... but it's so hard when your legs literally feel like lead (also, mine start burning sometimes after awhile). His solution was to get us a dog... so now I have an actual reason to get up and walk every day 😂

It's so great that you're doing these videos all week

You are so great! I love watching your videos. I have just been diagnosed with ms and it really helps me watching your videos. Keep making them. You are so inspiring.

Oh my god...hearing you describe how your legs felt after your relapse resonates massively with me. My legs failing me was my 2nd relapse and what lead to my diagnosis. At the time and to this day I was always describe it as my legs went numb from my waist down (but it started in my toes and worked its way up). While I wasn’t paralysed walking felt pretty bizarre like you say I could feel every little change in the ground. I couldn’t wear shoes or even trainers (it ‘hurt’), my balance was none existent and as it got worse I couldn’t feel where my legs were in relation to the ground. It was all so so strange and bizarre feeling. Wish I’d seen a video like this at the time (this was feb/March/April 2016). But would you believe through it all I still went to work daily (2 yrs on and I look back and wonder how) but at least I was up and moving, my biggest concern was that they would stop completely. Thank you for making these videos...even though I’m not so newly diagnosed anymore it really helps watching videos like these.

Thank you so much for this. I'm determined to get better and back into fitness because of you :)

All because of Lemtrada and a positive attitude. Keep going I'm on the same path 8 months post round 1 knock wood I'm crushing this disease. Feeling great to be honest. Keep at it we've got this! 🤗👌🏻

The best way to describe it to normal people. It's like drinking the most alcohol you ever have lol and that's what it feels like to have legs being under attack by M.S. or if you have sat on your foot to the point of being numb but you can still move it. Then the pins and needles thro out the legs too. You're a trooper, keep going

Wise, Smart, Versatile, Vibrant, and above all, BeautifuL woman ❤️

Thank you I ordered by TRX bar can't wait to get started

You are awesome :)

Izzy thank you so much for your videos. They have really reminded me to stay positive and made me feel less alone. Are you based in London?

Did MS affect your hands at all?

Lemtrada has such massive risks of cancers and such, why did you choose it?