tag:blogger.com,1999:blog-9141185645986617922.post1380700598221438832..comments2023-10-30T06:29:12.790-07:00Comments on G5 Family: Serengeti Smiles at the SD Wild Animal ParkShanna Grimeshttp://www.blogger.com/profile/01863808423565134938noreply@blogger.comBlogger1125tag:blogger.com,1999:blog-9141185645986617922.post-11279236637615934592008-03-06T07:36:00.000-08:002008-03-06T07:36:00.000-08:00Hi- found you through Trevor's site. I see you are...Hi- found you through Trevor's site. I see you are on the IS group... I read but don't absorb as well as I used to. I am not 100% familiar with Kaylee's story. BUT, I see someone has TS. Is it Kaylee or one of the other kids? I follow the TS forum because my son has a TS mutation but is not diagnosed with TS. However he's been on Vig for 3.5 years and they tend to have the most experience.<BR/><BR/>Anyway, good luck. I have three kids... one post IS, with dev delays, one 'neuro-typical' and one with PDD-NOS.<BR/><BR/>You can find me here<BR/>blogs.timesunion.com/austinbenconnor<BR/>JenJSmith5780https://www.blogger.com/profile/16954759123115546248noreply@blogger.com