Hi Everyone!

8 years ago, I was diagnosed with a rare subtype of MS called Tumefactive Multiple Sclerosis (TMS). It's so rare, that only between 2-3% of the entire world's population has it. When I was first diagnosed, there was and still is limited research and information on this type of MS. I spent the last 8 years, advocating and raising awareness for not only MS, but for TMS too. 

This is my second year of participating in MS Focus on Fashion and I'm honored to walk the runway and show others that MS does not define us and beauty comes in all forms. To help continue to spread MS awareness, I have partnered up with MS focus to help fundraise for MS Focus on Fashion. Every donation helps the cause and the immediate needs of us MS patients. Hope you all will continue to join the fight against Multiple Sclerosis! Thank you for all of your love and support! 

-Didi