Six years ago, mothers and fathers all over the earth were alone, believing their baby was the only baby with a hypoplastic RIGHT heart. There was no solid information, no active organizations, no one to represent them and their children.

That changed on August 15, 2003 when just a few mommies came together in a free Yahoo group to compare notes, and to spark hope. That hope burns bright today as Hypoplastic Right Hearts counts nearly 600 families in our membership. A 501 c3 dedicated to educating parents, advocating for patients, and fanning the flames of that precious hope - HRH is committed to illuminate the shadows and eliminate the loneliness that inspired its inception. No one needs to feel alone with this disease, no child is the only child, and every child matters.

Please help us celebrate today - and every day that children have survived this life-threatening disease. Every birthday of an HRH child is bittersweet, it is the celebration of miraculous survival with the shadow of painful memories of the fight it took to get to that day. We don't take any day for granted, help us celebrate the spirit that makes us shine and the hope that we hold for a brighter future for our children. 

Please consider a $6 donation, $1 for each year we've spent raising hope and educating families to become their children's strongest advocates.

Donating through this website is simple, fast and totally secure. It is also the most efficient way to support my fundraising efforts.  Many thanks for your support -- and don't forget to forward this to anyone who you think might want to donate too!

Heart hugs,

Amanda Rose Adams

Founder, & director of fundraising

Hypoplastic Right Hearts