Comments on: AFP testing, Trisomy 18 and my wife http://www.georgeallenmiller.com/2010/01/03/afp-testing-trisomy-18-and-my-wife/ One Geek's take on all things SciFi Sat, 07 Jan 2012 05:32:00 +0000 hourly 1 http://wordpress.org/?v=3.1 By: George http://www.georgeallenmiller.com/2010/01/03/afp-testing-trisomy-18-and-my-wife/comment-page-1/#comment-2915 George Mon, 04 Jan 2010 12:25:55 +0000 http://www.georgeallenmiller.com/?p=380#comment-2915 Hi Bianca, Trisomy18.org was on of the first websites I found a few minutes after we got off the phone with the doctor. A lot of really good information there. I'll be sure to register soon. George Hi Bianca,

Trisomy18.org was on of the first websites I found a few minutes after we got off the phone with the doctor. A lot of really good information there. I’ll be sure to register soon.

George

]]> By: Bianca http://www.georgeallenmiller.com/2010/01/03/afp-testing-trisomy-18-and-my-wife/comment-page-1/#comment-2908 Bianca Mon, 04 Jan 2010 03:28:24 +0000 http://www.georgeallenmiller.com/?p=380#comment-2908 I'm sorry to hear you are going through a difficult and stressful time in your pregnancy. Waiting for test results is nerve racking. If you haven't already found us, here is the website for the Trisomy 18 Foundation, www.trisomy18.org . You will find a wealth of information on Trisomy 18, along with many loving and caring families that have walked this journey. As we know, each child with Trisomy 18 is unique. While the list of known defects is the same, some children are more affected than others. I encourage you to register and join our support boards. You'll be able to communicate with other families awaiting further testing and families affected by Trisomy 18. Right now the best thing to do, is gather up as much information as possible. Please know our hearts are with you, and we're here to support you. Warmly, Bianca DeLone Staff at Trisomy 18 Foundation,Inc. BDeLone@trisomy18.org www.trisomy18.org www.trisomy18support.org I’m sorry to hear you are going through a difficult and stressful time in your pregnancy. Waiting for test results is nerve racking. If you haven’t already found us, here is the website for the Trisomy 18 Foundation, http://www.trisomy18.org . You will find a wealth of information on Trisomy 18, along with many loving and caring families that have walked this journey. As we know, each child with Trisomy 18 is unique. While the list of known defects is the same, some children are more affected than others. I encourage you to register and join our support boards. You’ll be able to communicate with other families awaiting further testing and families affected by Trisomy 18. Right now the best thing to do, is gather up as much information as possible. Please know our hearts are with you, and we’re here to support you.

Warmly,

Bianca DeLone
Staff at Trisomy 18 Foundation,Inc.
BDeLone@trisomy18.org
http://www.trisomy18.org
http://www.trisomy18support.org

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