Links to family web pages offering information &

support to other families Living With Trisomy




 About Chromosomes

Trisomy 01 (1 link)

Trisomy 02 (4 links)

Trisomy 03 (1 link)

Trisomy 04 (4 links)

Trisomy 05 (1 link)

Trisomy 06 (1 link)

Trisomy 07 (3 links)

Trisomy 08 (6 links)

Trisomy 09 (7 links)

Trisomy 10 (2 links)

Trisomy 11 (2 links)

Trisomy 12 (2 links)

Trisomy 13 (8 links)

Trisomy 14 (5 links)

Trisomy 15 (2 links)

Trisomy 16 (4 links)

Trisomy 17  (4 links)

Trisomy 18 (15 links)

Trisomy 19 (1 links)

Trisomy 20 (2 links)

Trisomy 21 (3 links)

Trisomy 22 (3 links)



Trisomy 13
Information & Family Support Links

Living With Trisomy 13 - Extensive photo albums and updates of children living with Trisomy 13, Trisomy 13 support and resource links, special information and support for prenatal diagnosis and other useful information.
The Healing Power of Prayer - Renamed TRIsoMY Favorite Things.  Web site inspired by Natalia - a five year old child with Trisomy 13 - 52 minutes in our arms, forever in our hearts - Bryson's Blog:  A weblog about my grandson who was born with Trisomy 13 In loving memory of  Bryan Fitzgerald King, full T13.  From March 17th to March 21st, 1981 you lived the only life you were meant to live... - We told our doctors that God knows the last day of this child's life and we don't want to be the ones to choose his last day.  Some asked how we could hold on to hope for Anthony given his diagnosis.  Our response was:  "We were asked to be his parents, to provide him with life, love, home and security.  That is what we are doing and we will do it all the days of his life."  Anthony's days were 6 shy of his 1st birthday.
Kia's Trisomy 13 Tripod Site
For help with "What You Need To Do" when you have a Trisomy 13 prenatal diagnosis...  There is a birth plan that will help ease the journey...
Becca's Story - A Trisomy 13 Mosaic Adult

Unfortunately, due to the large amount of spam that our "submit a link" page was generating, I have been forced to do away with that feature.  So to submit your rare trisomy child's website for linking, please use the below "Contact Us" and include the following information: your name, website url to be linked, which chromosome # to be linked under, website's title (if any) & a short description of your child's site.  I apologize for any inconvenience this causes legitimate rare trisomy submitters, but the spammers out number you at least 100:1.

     Contact Us     

All links from this site reflects each families personal journey with raising a Trisomy child. It is not meant to replace any medical advice of a professional familiar with your specific condition. The personal journeys in any parent's linked sites are only their opinions and their own journey with having a Trisomy child. You should consult with your own physician or other medical professional regarding the opinions or recommendations expressed within the pages as to your own child's symptoms and medical condition.

                                                                                  Site last updated: 08/01/16