Dear family and friends, Duchenne muscular dystrophy (a muscle wasting condition) affects young boys and in rare cases girls.
Currently there’s no cure and no one survives.
As many of you know, our two boys Riley and Tarek were diagnosed with this devastating disability in 2016. Since then our lives haven’t been the same. The doctors appointments, therapist appointments, grief and daily stresses have now become our new normal but no matter what we face we will do whatever we can to help find a cure for our boys.
On the 28th of February 2020, Elie Eid, the founder of Save Our Sons, along with myself and a group of walkers will be walking 186 KMS over nine days across Melbourne, visiting schools of Kids with Duchenne to raise vital awareness and funds.No matter how tough this may be for me physically, it does not compare to the lifetime of hardship that kids and families living with this cruel condition have to endure.Your donation, no matter how big or small will go a long way in making a difference in their lives today.
Thank you in advance for your generosity.