Hi! I like your website. My cousin has a rare disease called vater syndrome, and I wish people would treat him normally or find out about vater syndrome so they understand him better. G2G Bye!
Kelsey G.
WI USA -
i like this page cuz i feel that many people should no about this syndrome!!
ashton h.
vidor, tx USA -
Hi this is Alison I am doing a science project and I chose this disease along with my partner. I am in 7th grade and if I met Kelsey I would enjoy her a lot. I have some friends with down syndrome. I treat them just like ordinary people and I think that that is very wrong for you not to be able to get married. My cousin Lauren is with me and when we saw that website about Kelsey and what she said we both said that the law is wrong. Well I have to go and finish my report. Thank you.
PS I enjoyed this web site
Alison Briscoe
Alison B.
Maineville, Oh USA -
Thank you for the personal info, which we find more easily absorbed than much of the "expert" web sites. We think our daughter who was born with hypotonia has PWS and have unconsciously already started on some of the "good practise" you suggest.
We hope all goes well with you and God bless.
Julie and Jonathan Spencer <JSpencer@nationwideisp.net>
Lewes, East Sussex, UK -
Thank you for letting me know about this terrible disease. All the best to Kelsey. And keep it up, the Team.
Gilbert
Mauritius -