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Click Member link to see site in tv***** Millie! The CHD community POSTER CHILD!!! ******
Millie was in the hospital for 9 days, she got released yesterday. She was at Children's{;} Hospital and Medical Center in Seattle. I spent the entire week staying with her. It feels{;} good to ...

Our Beloved Son
My son has TOF and this site describes that experience from my point of view as his mom.

Heather
Heather Mae Bonham was born on January 13, 1991, it was the happiest day of our lives. To see this beautiful baby girl that we had wanted and longed for finally arrive into our lives. Heather weighed in ...

Zachary's Zoo
The story of our son Zachary who was born 3/10/98 with a variety of complex congenital heart defects. He completed his three surgeries at the University of Michigan Medical Center by Dr. Edward Bove. ...

Congenital Heart Defects community
This is the home page for the CHD community at communitysurf. Visit this page to{;}add your site or edit your site. See the latest news and the community statistics here. Get help from the community ...

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: communitys and more!
a site of communitys and more! my son and my daughter have congenital heart disease which is why I am joining this community. . .

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 ...

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 ...

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 ...

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 ...

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

Cody Maulden
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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 community 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, ...

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 ...

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 ...

Joshua Thomas Spencer
Josh is 6 with HLHS. He has had 3 open-heart surgeries. He is in 1rst grade. He is doing great thanks to God.

Heart Kids in Australia
Tracking the journey of our 3 year old toddler who has undergone open heart surgery twice (requicommunity further in the future) has now moved to an Internet Uptrade challenge to raise funds and awareness ...

Suggs Family
Just the usual in the suggs family

all things izzy
izabells page

Gabriel's Heart
This is where I rant and rave, whisper and shout, but mostly laugh. A lot. I really let my crazy shine through as I grapple with my son's upcoming heart surgery and the details of a full time working mama ...

Dallas Kaylie-My Story
A site dedicated to those with heart defects in hope of encouraging them.

Gabriel's Heart
This is the story of my life with Gabriel, my second Wonderbabe. Born with Transposition of the Great Arteries, this is where I rant and rave, get my crazy on, laugh hysterically, but most of all love ...

Herding Cats (Sadie's Continuing Story of TGA)
A mom's perspective on having a toddler with CHD (TGA). While most of the blog now focuses on daily life for this family, early entries explain in detail the daily battles they faced, and how it led the ...

The CHD Blog
News, Information, Stories and Commentary on life with CHD.

Nick'sNewHeart
I have already join and been OK but have had trouble they HTML on my site. Now I can't get communitysurf to let me convert. Could you help me with any of this. Also, I saw that my site does appear on ...

RSTCA - Our Family
This site is all about me and my family, including my son Toby who has had to have heart surgery, and my daughter who has a rare chromosome disorder called 'Community22'.

RyansHeart


5 Little Men


Two Beautiful Blessings
Our youngest daughter was born with a serious congenital heart defect called Transposition of the Great Arteries. This site is all about how our family keeps our faith in God ducommunity the good times ...

Inspicommunity Hearts living with congenital heart disease
I thought I would start a blog of adults with Congenital Heart Disease. Instead of talking about their disease, talk more about the stories, and how they see life. I want to ask a series of questions ...

Mom 2 Andre
I'm a stay-at-home-mom / stay-at-home-mum (SAHM) from Australia. On May 1st 2008, I gave birth to a beautiful baby boy who was born with a Congenital Heart Defect (CHD) known as Severe Pulmonary Stenosis, ...

Our baby's journey with Hypoplastic Left Heart Syndrome
Diagnosed in utero at 20 weeks with HLHS, our son, Mason Stephen Terrazas, has been one tough cookie. Join us for a glimpse of Mason's journey, including photos of his Norwood and Glenn surgeries. ...




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