NO ONE SHOULD FACE MS ALONE!
Hey guys! 🌻🌻🌻
Quick recap: I was diagnosed with Multiple Sclerosis at 17, absolutely zero stars, do NOT recommend. After surviving some truly catastrophic life chapters, I’ve emerged as the sunflower-loving, chaos-embracing, MS-advocating lass you see before you. Now my only goal is to drag you around a lake with me in May for a good cause. Come for the steps, stay for the ridiculous selfies and yes, a t-shirt may or may not be involved ✨
For the uninitiated: Multiple Sclerosis is a chronic, often relentless disease that attacks the central nervous system - the brain, spinal cord (myelin), and optic nerves. It’s the most common neurological disease in young adults, and three out of four people living with MS are women and absolutely no cure….yet!
Having MS is heavy, but don’t worry, I won’t cling to your shoulders (probably). Just come help me carry some of my big, unwieldy feelings while I try to look like I have my life together.
Whether you join me in person, donate schmeckles 🤑, or just quietly cheer me on from the couch, your support helps people with MS access services like MS Plus, MS Peer Support, and MS Employment Programs and brings new treatments closer to reality.
So let’s walk, run, roll, and crush this MS-Y situation together. 💪
Follow my chaos on Instagram @circularblooms for updates.
From me and 37,756 other Australians living with MS: THANK YOU. Now go forth and KEEP S’MYELIN 💋
Our Achievements
