#SMA is very near and dear to my heart and the hearts of my family.
In 1998, I was blessed with a beautiful and seemingly healthy little girl.
Brooke was the JOY of my life !!
Only 5 short months after her birth, we learned through diagnosis that Brooke had Spinal Muscular Atrophy, better known as SMA.
Our lives were forever changed that day when she was diagnosed, although we continued to find strength and hope in the resources and care we found in the community of others walking this journey with us in the SMA community.
#FamiliesofSMA was a vital source of information and support as my family dealt with the reality of SMA.
August is #SMAawareness month and each year, in memory of my daughter Brooke, it is my honor to give back to the organization and the community who gave so much to us during our time of need.
I ask you to please help me #raisefunds for Families of SMA as they continue to provide resources, support and search for a #CURE of this horrific genetic disorder.
To learn more about Brooke and our story please visit us @ https://www.facebook.com/MySMAAngel
3 ways you can help support:
Shop all your favorite Avon~PamperedChef & Norwex products + receive FABULOUS discounts & specials all while supporting #CureSMA from July 1st-July 31st 2020 by following this link http://www.ashleyslilshop.com/sma-awareness-fundraiser.html#/
Thank you for your support,
TOGETHER WE CAN FIND A CURE!!
In Loving Memory Of Brooke
June 11, 1998~December 18, 2002
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