Hello,

Many have you been along on this journey with me since 2016 when my dearest friend Carolyn's son Kiran was diagnosed with Cystic Fibrosis. For those of you new, welcome.  I try each year to do my part in helping raise awareness and dollars for the Cystic Fibrosis Foundation to fund research to help continue the journey to find a cure for this disease.

Cystic Fibrosis is a rare, life-shortening genetic disease that affects approximately 40,000 Americans and just 100,000 people worldwide.  . Kiran is strong-willed, precocious and compassionate and we know that his future is bright due to the work of the Cystic Fibrosis Foundation. He just celebrated his 8th birthday along with his twin brother Raj.

Please consider donating any amount to my efforts, I would greatly appreciate your thoughtfulness and support.

love,

Katie