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Trisomy + ADD YOUR SITE (27 members)The Trisomy Community 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 Community is to connect, parents, families and other interested persons. {;}{;}In order to be added to the Trisomy Community, 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.{;}
The Upson FamilyThis 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 PageMy Site about other autoimmune disorders and other links like trisomy and links for mental disorders.
Miracles in Progress-Living with Trisomy 13Miracles in Progress - Living with Trisomy 13
Photos, Support and stories for pre-natal diagnosis, Links to support groups
for Trisomy 13
Elrics home pageElric 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-LineThe 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 ducommunity our walk in the unknown.{;}
Abigail WheatA 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 ValencicThis 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 WarpehoskiThis 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 PHARMLife story and pictures of a young adult living with both Partial Trisomy 6p and Moya Moya Syndrome.
Abigail Grace WilsfordOur precious daughter Abigail Grace had Trisomy 18. Although she only lived a few days she blessed us for a lifetime.{;}
The Adventures of EthanManWe offer this site in honor of our son, Ethan, who was born with Trisomy 13 and only stayed with us for seven weeks. The site contains information on Ethan's specific features & symptoms, the seven week progression of his life, and a light-hearted superhero motif that laughs in the face of T-13. We hope it helps others facing similar difficulties.{;}
Down syndrome - more than just an extra chromosomeA mainly Swedish page with a small english part with information about our son and how we stimulate him. There are some nice pictures too. There is a small Czech part too.{;}{;}En informativ sida om downs syndrom skriven med de kunskaper jag skaffat mig tack vare vår son. Här finns att läsa om språkutvecklingen, motorikträning barnomsorg m.m.{;}
baby2angels2000a memorial to our two little angels...Gareth, who had trisomy 18 and Dominic, who had a cystic hygroma.{;}
Brandon's MemorialA memorial site for Brandon, who had Trisomy 18. A collection of photos, narrative and links.{;}
Fabio's Down Syndrome HomepageFabio's story, pictures, poems and useful information on Down Syndrome as well as links and addresses of Down Syndrome Organizations and Parents Groups in the U.S. and worldwide. A German version of this website is also available.{;}
Jacob's DenHi! My name is Jacob. I am 16, I attend High School in Rockville Center, and I have Down Syndrome. Welcome to my Homepage! I like to play baseball, ride my bike, play Ninetendo, drive boats, and play with my six sisters and one brother.{;}{;}
Our Natalia-The Healing Power of PrayerPhotos, journal of first year to friends, and prayer site.
Trisomy Net Community HomepageThe Trisomy Community 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 Community is to connect, parents, families and other interested persons. {;}{;}In order to be added to the Trisomy Community, 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.{;}{;}
Rainbows Down UnderThe main focus of this site is information relating to Trisomy 18, Trisomy 13 and other related chromosomal disorders. It is my rainbow on the web dedicated to families and children everywhere who are effected by Trisomy 18 and other rare Trisomic disorders.
Susanna's pagesThis site is dedicated to the memory of our daughter, Susanna, who was born with Trisomy 18.{;}
Rainbow AngelsThese pages are for remembrance, reflection, inspiration and love. {;}{;}They are dedicated to {;}Taryn, Louise, Melissa, Susanna, Rayne, Rachelle {;}and all the precious children who have received their wings. {;}{;}Their lives were too short, but will be long remembered..... {;}{;}These precious children were all born with Trisomy 18 (Edwards Syndrome) a chromosome anomoly. {;}
Susanna's pagesThese pages were made in memory of our daughter, Susanna, who was born with Trisomy 18{;}
Grace Anne Nugent- A Celebration of LifeThis is the story of our journey with our daughter Grace who was born with full trisomy 18. She lived for 2 months. She was a blessing and a gift. Her story is one of hope to families that get a fatal diagnosis.
Leyna Marie Holstine`s trisomy 18 journeyWe made this web page in memory of Leyna Marie was born and got her wings at the 23September2005. She had a condition called Trisomy18. We love and miss her very much!!!
