---

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.{;}

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

Abigail Grace Wilsford
Our precious daughter Abigail Grace had Trisomy 18. Although she only lived a few days she blessed us for a lifetime.{;}

The Adventures of EthanMan
We 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 chromosome
A 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.{;}

baby2angels2000
a memorial to our two little angels...Gareth, who had trisomy 18 and Dominic, who had a cystic hygroma.{;}

Brandon's Memorial
A memorial site for Brandon, who had Trisomy 18. A collection of photos, narrative and links.{;}

Fabio's Down Syndrome Homepage
Fabio'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 Den
Hi! 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 Prayer
Photos, journal of first year to friends, and prayer site.

Trisomy Net Ring Homepage
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.{;}{;}

Rainbows Down Under
The 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 pages
This site is dedicated to the memory of our daughter, Susanna, who was born with Trisomy 18.{;}

Rainbow Angels
These 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 pages
These pages were made in memory of our daughter, Susanna, who was born with Trisomy 18{;}

Grace Anne Nugent- A Celebration of Life
This 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 journey
We 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!!!

Women & Children
Dedication to our son David who passed away from Trisomy 18. Along with our in Memory page, our website is dedicated to Women & Children's Health.

Emily's Page
Meet Emily Stauffer, our miracle baby born on July 9, 2001, diagnosed with full Trisomy 18 and expected to live as little as a few days but most certainly not more than a year. She is now 4 1/2 years old and an absolute doll. Despite her physical and mental disabilities and limitations, she brings such joy to our lives and offers a beacon of hope to others faced with the possibility of having a child with special needs. She also proves without a shadow of a doubt that there is a God and He is alive and well and moving on planet earth! In her four + years, she has totally flabbergasted the medical community with her life and her miraculous story that includes a supernatural healing from hepatoblastoma (childhood liver cancer) without medical treatment. Through megadoses of prayer, The Great Physician took care of her cancer resulting in a healed, happy, beautiful little girl full of love and personality. Her full story with photos can be found on her web site at http://home.supernet.com/~gfeinc/ Be encouraged and blessed by God's amazing testimony in our Emily.

---