---

RING DESCRIPTION: Personal websites about congenital heart{;}defects. Congenital Heart disease affects one in one hundred babies, it is the most common birth defect. Read our heart warming stories. Watch our children grow up. Most of our children are living and doing well, but many have lost their battle with CHD..

Please click one of the links below to enter the RingSurf Viewer. JOIN RING NOW

Chaney's Memorial Website
A memorial site for little Chaney, who had Hypoplastic Left Heart Syndrome. (3/3/03-3/6/03)

Dallas Kaylie's Story
Dallas' story of being born with a heart defect

rachellenet: webrings and more!
a site of web rings and more! my son and my daughter have congenital heart disease which is why I am joining this ring. . .

Laura's Memorial Page
On this page you will find a story about my daughter Laura Paige. She {;}was born 6-4-02. A few days later we discovered she had several congenital heart defects. Tragically she died when she was 11 days old after having unsuccessful heart surgery at MCG in Augusta, Georgia.{;}Laura had: IAA, VSD, and BAV{;}

Samantha's Space
This website tells of our daughter's journey with Hypoplastic Left Heart Syndrome (HLHS). It describes our emotions as we faced her three open heart surgeries and details her progress as she has grown into a beautiful little girl.{;}

Jackson's Page
"This site is dedicated to our precious and brave little son, Jackson Eggleton who was born on 22nd of October 2001 with congenital heart disease. We are an Australian family and Jackson was our first born child. He passed away when he was two and a half months old and unfortunately didn't make it to open heart surgery." {;}{;}

K.J's Page
This web site is dedicated to a little boy who even when he was still in the womb was read bible stories and prayed with. K.J. has HLHS and is awaiting his 3rd surgery. Come see our special boy, one look at his smile and blue eyes will steal your heart.{;}

Millie is thriving
Millie was born with 3 VSD's, Coarctation, Bicuspid Aortic Valve and she is thriving!{;}

Cody Maulden
{;}

Special CHD Kids
Special CHD Kids is a Web Page{;}for Parents with Children Living with{;}Congenital Heart Disease. We offer support & friendship, resources, Congential Heart Defect information and so much more.{;}

Dillon's Heart Story
the webring page for an oklahoma heart family. come navigate our site and meet dillon, our heart baby. dillon is 5 years old now and was born with tga, vsd, iaa and ps but he is doing GREAT!!!

Maeve's Page
Maeve has complete atrioventricular canal defect. Read about how she's doing and what she's been through.

Dextrocardia with Situs Inversus
Dextrocardia with Situs Inversus. Cause, Diagnosis, Treatment, Forums {;}and other information about this rare disorder.

Cheyenne's Place
Hello, friends we hope you come to visit Cheyenne's page. My name is Michelle, and I am a single mom to a little girl with a special heart.  Cheyenne was born with a very rare CHD, Tricuspid Atresia, which means she is missing the valve between the two right chambers of her heart. She also has Severe Pulmonary Stenosis, and she is an ECMO survivor.  It has been a long road for her, but she has been a brave soul and fought every step of the way. She is stronger than I could have ever imagined.

The Justin Dunn Congenital Heart Foundation
This site presents the "heart journey" of our son, Justin, who was born April 2, 2000 with near pulmonary atresia w/IVS and a hypoplastic right ventricle. We have created a nonprofit foundation to raise money to support CHD awareness and family support. Please support our cause by donating, and ordering your "Heart of a Child" CD or personalized "Mending Hearts" baby quilt.

Johnathan Spencer Joplin
Memorial to my sweet little HLHS angel.

Gage Hunter Betancud, Living with Tetralogy of Fallot
Our site is devoted to our son Gage and his courageous fight with a severe congenital heart defect. He was born 5 weeks premature with Tetralogy of Fallot November 11, 2001. This is his story.

Robert Plotnek - My Life As A Heart Child
Robert Plotnek, the story of a heart child, who was born with serious congenital heart disease and who eventually had to be transplanted at the age of 9.

WisdomHeart
Sophia was diagnosed with a CHD called Tetralogy of Fallot w/pulmonary trunk atresia and DiGeorge Syndrome. This weblog provides frequent updates regarding her treatments and surgeries.

Brandon's Web Site
This site is about Brandon, a child born with tetralogy of fallot with absent pulmonary valve. There are pictures of him, including in the hospital, and of his little brother. There are also links to some heart information.

---