Disease makes people–myself included–uncomfortable. I started It’s Only A Bruise to facilitate conversation about multiple sclerosis between myself and my friends after I was diagnosed with relapsing-remitting MS in 2013. The internet is a scary place during diagnosis. There’s so much unknown and, at the same time, too much information out there. I strive to make IOAB the resource that I wish I had in the early stages of my MS. And so, my audience grew to include others with the disease and I now write for multiple online MS resources, as well as my blog, and I advocate across multiple social media platforms. This is my story. And it doesn’t end with MS.
West Allis, WI
She’s awesome and writes from the heart.
Cat Stappas is living with MS & making people aware of this disease from a personal standpoint. She provides knowledge that would not otherwise be available to the readers of her blog. She is living with this disease; but she is not letting the disease stop her from living. She & her husband, Rusty, walk & bike for a cure.
Cat Stappas provides information on MS that raises our awareness of this disease. She is on various social media sites; and each one provides an avenue to learn more about her personal journey with this autoimmune disease. Cat and her husband, Rusty, also raise money through MS Walk and Bike MS to fund research for a cure. They are warriors! — Sally
Best in Show: Twitter Nominee
Best Kept Secret Nominee
Health Activist Hero Nominee
Advocating for Another Nominee
Best in Show: Blog Nominee
I’m a Patient Leader