Guest guest Posted November 22, 2004 Report Share Posted November 22, 2004 Welcome to our family! What is your name? Where do you live? What is your grandchild's name? Alice Poholsky cell Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 23, 2004 Report Share Posted November 23, 2004 Hello, I am Horn from east Texas. The grandmother of 4 month old who lives in Tulsa. The geneticist suspects he is mosaic, but its not official yet. He shows little signs of Downs and is a Tet baby. Ironically he just had an emergency shunt surgery this weekend, we got home a couple hours ago with his two sisters (4 and 8 yr. olds) and will take them home next Sunday weathered the surgery just fine and the cardiologists says he hopes he has bought enough time to delay the rest of surgery in 6-9 months. Tulsa has a great Downs program, but theres no support group or etc within 100 miles to me and I'm always searching the web. So glad I found your site, the first such I had found on mosaics. I bet I've downloaded reams of paper dealing with Downs and now mosaic, ditto on Tetralogy of Follet....I'm kept busy educating (as much as I can!) my family and friends. And believe me there are some who really needs educating! I just learned theres a lady in my community who has a 19 or 21 yr old son, and she's writing a book about her experience and life with the son. I want to contact this person, but not sure whether I'd be intruding. This is all so new to me, and I really do hunger for contact with parents of and the children themselves. I've downloaded all the personal stories from your web site and spent hours reading them. Thanks for allowing me to join. Sandy Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 29, 2004 Report Share Posted November 29, 2004 Hi ! Where in East Texas are you? I am in a small town called lin, just between Waco and /College Station. I am glad to hear that is doing well from his surgery. It is amazing how much a little guy can go through! You will find that our support group is unique. Because we are online, we can offer support on a daily basis, vs the monthly support groups. Also, most support groups for Ds do not offer the information that families need when they have a child with MDS. Please tell 's parents about our group as well! We would love to offer support and information to your whole family! Perhaps, you and your family can make plans to join our IMDSA conference in Houston this coming June! We would love to see you all there! Kristy Colvin IMDSA President Become a member of IMDSA today at http://www.imdsa.com ************************************************* Learn more about MDS http://www.mosaicdownsyndrome.com ************************************************* Contact IMDSA Today at: IMDSA~PO Box 1052~lin,TX~77856~USA~1- ************************************************* Quote Link to comment Share on other sites More sharing options...
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