I was diagnosed with SMAS while the non-profit was still being born. The non-profit has helped so many warriors in the last 7 years (can’t remember the exact date the non-profit became to be) with grants and even with building files of Drs and surgeons who can help with SMAS. There’s a network of SMAS warriors on Facebook and instagram that helps with support in all ways possible and now raising enough money to start research for SMAS. I have donated to the non-profit in many different ways, from, making quilts for warriors in the hospital having surgery, to donating birthday funds to the non-profit, and helping with online auctions and other fundraisers.
The non-profit goes above and beyond to help SMAS warriors with anything they may need help with and I’m proud to be part of this non-profit.