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Trisomy





RING DESCRIPTION: The Trisomy Net Ring was created for those who wish to share their web sites about Trisomy children and/or their families or have pages with information about this disorder and/or related problems. {;}{;}The purpose of this Trisomy Net Ring is to connect, parents, families and other interested persons. {;}{;}In order to be added to the Trisomy Net Ring, you must have a web site about a Trisomy child including, but not limited to, Trisomy or any other Chromosomal disorder. {;}{;}It is our intention to spread the word that these children are very special and their lives are precious.{;}



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The Upson Family
This site is about our family, to include our daughter, Audrey Grace, who was diagnosed with Trisomy 18 at 16 weeks gestation, made it to term and lived with us for almost seven months.

My Other Autoimmune Disorders Page
My Site about other autoimmune disorders and other links like trisomy and links for mental disorders.

Miracles in Progress-Living with Trisomy 13
Miracles in Progress - Living with Trisomy 13 Photos, Support and stories for pre-natal diagnosis, Links to support groups for Trisomy 13

Elrics home page
Elric was born on the 19:th of December 2003. He had a rare chromosome disorder called Trisomy 13 (or Patau\'s syndrome) and could only stay with us for 13 days. On this web page we are telling Elrics story, both because we want everybody to know what a lovely little baby he was and because we want to share our experience of this rare diagnosis with others.

Pass Pages
{;}This site is dedicated to our daughter Louise. She had Trisomy 18. Come visit and meet us!!!

Trisomy On-Line
The Trisomy listserv is an e-mail based support group for families, friends and health professionals who share a common interest in the rarer trisomy conditions. The technology of the internet offers us the unique opportunity to share our information,joys and sorrows, offer support and comfort to one another during our walk in the unknown.{;}

Abigail Wheat
A group of pages and photos dedicated to our angel Abigail. She gained her wings due to trisomy 18. She will always be a part of our family. She will always be loved.

Joseph Daniel Valencic
This is a site dedicated to our son Joseph Daniel Valencic, who only lived from July 19, 2001, to July 31, 2001, due to Trisomy 13 and the problems it caused in his body. It is a way for family and friends to remember him fondly, and to share our feelings about this experience.{;}

Jessica Riley Warpehoski
This site is dedicated to the memory of our daughter, Jessica, who was diagnosed with Trisomy 18. A moment in our arms, forever in our hearts.{;}

WELCOME TO PHILINA'S PHARM
Life story and pictures of a young adult living with both Partial Trisomy 6p and Moya Moya Syndrome.

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