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 18
Information & Family Support Links

Keren Elyse - This site includes lots of photos and letters to friends about Keren

Jonas' Story -  Isochrome 18q mosaic

Mieko  - lives with full trisomy 18. She was born 3/09/04.
Morgan's Story - Partial Trisomy 18/ Partial Deletion 9
LittleClaire - Claire was diagnosed with Trisomy 18 and wasn't expected to live full term. She is still with us years later.
Lachlan's Story - Trisomy 18 mosaic  Lachlan's Australian Trisomy Journey
Lachlan's Trisomy 18 Blog
Robert English - Partial Tetrasomy 18
Allison's Trisomy 18 Journey - Facebook
Rebekah Faith Trisomy 18
Redefining 'Incompatible With Life"
Brandon's Mosaic Trisomy 18 Journeyl
Shelby's Story: Living With Trisomy 18
Jezreel's Story - Trisomy 18
Erin's Story - Trisomy 18

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