Saoirse has been our Butterfly Bee since before she was born. At about 6 months pregnant we learned that our baby has Hypertrophic Cardiomyopathy (HCM), which is a thickening if the heart muscle. Although we’ve had a number of scares Saoirse has always fought and is thriving as a 2 year old.

Please consider donating to this great cause who is fighting for kids like Saoirse.

September is Children's Cardiomyopathy Awareness Month and the time to raise awareness of pediatric cardiomyopathy, a chronic and potentially life-threatening heart disease. Join me and Team CCF during the entire month of September as I Walk for Cure to support children with cardiomyopathy and their families.

Please support my walk efforts and help me meet my fundraising goal. All walk proceeds will go towards funding CCF's Family Assistance Program and family support services. Your support means a great deal as this is a cause that is meaningful to me.

The Children's Cardiomyopathy Foundation (CCF) is a national 501(c)(3) organization focused on accelerating the search for causes and cures for pediatric cardiomyopathy. Since 2002, CCF has grown into a global community of families, physicians, and scientists dedicated to improving diagnosis, treatments, and quality of life for children with cardiomyopathy.