Nicholas Viner Heart Foundation 

Heart Warriors

Rocky's Road 

This page was created by Garek and Raychel Renk to keep you informed about Rocky; so you prayer warriors know exactly how to pray for our little fighter.

Joseph "Jojo" Katsuleres

Our baby boy is due in May and has been diagnosed with severe heart defects and other issues related to heterotaxy syndrome

Evie Our Miracle

Evie Cheryl Houston Fraser Born with Heterotaxy Right Atrial Isomerism, Asplenia, congenital heart defects TAPVD, DORV, AVSD, Sub PS.


Jasmine Winning was born 09/23/2014 with Hypoplastic Left Heart and Heterotaxy. Please pray for hope and strength as she battles her way through.

Graysen's was born with many heart defects and a condition called heterotaxy. Follow his journey with us.

Violet is full of spunk and character! Her CHDs will not bring her down! <3 Diagnosed with Heterotaxy and Scimitar Syndrome. 2 OHS to date!

Sebastian's Heart

Sebastian James Leader. My heart warrior, due to be born on the 22nd of December 2015 with Hypoplastic Left Heart Syndrome. This page has been set up as a point of contact for my friends and family.

Dawn-louise's H.L.H.S Blog

This group is used as a sort of  "diary of events" around Dawn-louise's journey with Hypoplastic Left Heart Syndrome (H.L.H.S), including her operations, recovery, doctors/ hospital appointments, and also things She has accomplished or was told she would never be able to do, along with days that have importance to us.

Follow the story of Lincoln and his new heart.

Our son Carson was born 12/12/12 with a complex heart defect & Heterotaxy. This will be our new update page as we approach his next surgery on 4/30/15.

Brooklyn the Brave

Brooklyn has been diagnosed with Heterotaxy Syndrome. For every 1,000,000 babies born, 4 of them will have Heterotaxy! Brooklyn underwent 10hours of open heart surgery when she was 22 minutes old!

This page is to share my son's journey with friends and family.

Andrew was diagnosed with pulmonary atresia w/IVS and hypo plastic right heart syndrome.

Kai was diagnosed with a severely dysplastic mitral valve and he had to have a mechanical mitral valve placed at 7 months old.

Light Up the Darkness with Dawn

Dawn Isabella Willow Logan is a girl with Down Syndrome and Congenital Heart Defects.  Lighting up the Darkness one day at a time. 

Caroline's Crusaders

This page is to update our family, friends and supporters on Caroline's heart journey.

Super Heros Fighting CHD with Malachi 

This group is support and prayers for my 7 year old son Malachi he was born with CHD half a heart,  Hes had 3 heart surgeries already please join our journey keep it clean no trolls.

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