My Personal Fundraising Page

Thank you for visiting my fundraising page! I am participating in the Congenital Heart Walk to support the mission of The Children's Heart Foundation: to advance the diagnosis, treatment, and prevention of congenital heart defects by funding the most promising research.

I hope you'll join me by supporting my fundraising efforts as I work to raise funds for life-saving research.

ABOUT TEAM EMMA FAYE!

Thank you for visiting our fundraising page!

Every 15 minutes, a baby in this country is born with a congenital heart defect (CHD), making CHDs America's most common birth defect.

We are participating in the Congenital Heart Walk to support the mission of The Children's Heart Foundation: to advance the diagnosis, treatment, and prevention of CHDs by funding the most promising research.

Will you join us? By supporting our team or joining us in our walk, you're supporting research that will help save and improve the lives of babies born, and children and adults living, with CHDs.

We hope you'll join us by supporting our fundraising efforts as we work to raise funds for life-saving research for Emma and so many other heart warriors like her. 

On 11/22/22, our beautiful daughter, Emma Faye, was born. Emma joins many other babies out there (1 in 100) having been born with a CHD. Emma had her first open heart surgery at 7 days old and will require her next one this year, as well several more throughout her life. She's our little heart warrior!!!

We feel fortunate that medicine and technology have advanced so much in order to help her and others like her - but there is still more work to be done. Although CHDs are the most common birth defect, the research in this area is severely underfunded. 

Please help us raise funds and/or awareness, and we would love for you to join us on the walk on 5/13/23!

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