A MESSAGE FROM Miles for Mila
My sweet daughter Mila was diagnosed with CF at birth. My wife and I were completely taken with emotion and gratitude for the tremendous support we received from all our family and friends since she came into this world.
Mila just turned 2 years old in August and she is simply AMAZING! Mila has breezed through all her routine Doctor visits, she completes her daily treatments like a Champ and we continue to see Mila as a beautiful gift from God, capable of anything she sets her mind to! We believe that with the power of love and faith - anything is possible! And we have no doubt that Mila will continue to thrive and live a long, happy and healthy life.
On Sunday November 6th I will running the NYC marathon alongside my great friend and partner in this fundraising event Jeff. We are a part of the Cystic Fibrosis Foundation's NY chapter called THE BREATE TEAM.
Please consider donating so we can find a cure for CF once and for all.
Mila just turned 2 years old in August and she is simply AMAZING! Mila has breezed through all her routine Doctor visits, she completes her daily treatments like a Champ and we continue to see Mila as a beautiful gift from God, capable of anything she sets her mind to! We believe that with the power of love and faith - anything is possible! And we have no doubt that Mila will continue to thrive and live a long, happy and healthy life.
On Sunday November 6th I will running the NYC marathon alongside my great friend and partner in this fundraising event Jeff. We are a part of the Cystic Fibrosis Foundation's NY chapter called THE BREATE TEAM.
Please consider donating so we can find a cure for CF once and for all.
Until it's done!
With lots of love,
Nick, Jeff, Kelly, Luke and of course Mila
With lots of love,
Nick, Jeff, Kelly, Luke and of course Mila