Through advocacy, raising awareness and fundraising to support promising scientific research, Best Day Ever Foundation is on a mission is to extinguish Duchenne Muscular Dystrophy, a progressive and fatal muscle wasting disease affecting about 1 in 5,000 boys. Our founder's son, Jordan McLinn, is one of those boys. With the help of our community partners, we are also on a mission to help families affected by life-threatening medical conditions live life... one BEST DAY EVER at a time! Contact us to learn more about how you can join us on this mission!
Best Day Ever Foundation is a registered non-profit 501(c)3) and all donations are tax-deductible. EIN #81-1358629
A NOTE FROM OUR FOUNDER...
Best Day Ever Foundation was "born" in my heart a few years after my son, Jordan McLinn, was diagnosed with Duchenne Muscular Dystrophy. A few years into our journey, I realized I had immersed myself so deeply into trying to find treatments, the best doctors and scientists in the field, the best possible care, and I was always looking for ways to create really awesome experiences for my son. But... other members of my very own family were sacrificing, hurting and needing support too, especially my daughters. My entire family inspired the formation of the Best Day Ever Foundation. Our mission is about raising awareness and trying to find a cure for Jordan and others living with DMD... but it's also about helping all family members who have children with life-threatening illnesses live life... one best day ever at a time. Thank you for joining me on this journey of hope and life.
With Love & Gratitude, Laura McLinn
We are so grateful for our community partners and sponsors!