I also don't view myself as a sufferer - diagnosed almost half a year ago. Neuro said I've had MS for years. But today, i feel good! No big symptoms at all. Just very mild symptoms occasionally
This is a great idea!! I’ve always said I am a MS thriver since I was diagnosed so thrilled others feel the same way! Will definitely be taking part!!!
Your channel has made my journey with MS easier and more appreciative of every single day. Though very hard to cope with the diagnosis at first, struggling with symptoms for almost a year and not knowing what it may have been at the time. I tell myself most days that it will not hold me back in life in my aspirations and dreams. Thank you so much for your words of encouragement. Keep up the great work!
Firstly I want to tell u that when I feel bad I search yr videos because you push me to stand up again Thank you for your positivity You are our angel 🥀
Hi I just got diagnosed with RRMS MS in Jan 2019 and my mom has it too, 5 years. I still work, hike, swim, and what ever I want to do. I might just do it differently or slower. 😂 And my mom lives all over the world currently Mexico. She has been a huge supporter of my day to day life. I have my off days but I like to think positively ☺️ Everyday is better then yesterday because today is a new day ☺️
Yes 🤗. I say I’m blessed with MS ✨ I’m finding as of last year my right leg/foot drop is kinda off - not repairing or repairing sloooooooooooooowly 🐌. But such is life. Just get on with it 🤷🏽♀️ I love to dance and I laugh at myself with my awkward bop 😆
I love this... I'm a thriver and hoping to build my channel to spread some positivity for MS too... early days! Diagnosed 2011 and still owning it! I'd love to take part in a Thriving Thursday 👌🏽
I've been planning to start my RU-vid for a couple years now, I've been diagnosed for 6 1/2 years. You really are an inspiration let's collab in the future 🤘 stay optimistic 💯❤
My brother was recently diagnosed and he has like an aggressive form. He is currently doing rounds of seriods and chemo. Did anyone else have this type if treatment and how are you doing now? Is there anything you guys recommend that would help in decreasing flares ups?
