A Trisomy 18 Journey - Abigail Grace Wilsford
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Tuesday, January 10, 2012. or at least sit still long enough to snap a couple of shots. Monday, December 26, 2011. Do that x 6 for .
Saturday October 7, 2017. We Are Here For You. We have monthly support group meetings the 2nd Monday of every month at the Massillon Family YMCA.
Before I formed thee in the belly I knew thee; and before thou camest forth out of the womb I sanctified thee. Monday, November 14, 2011. I just wanted you to know I love you! Thursday, October 20, 2011. 38 weeks and 1 day. Tuesday, August 23, 2011.
For Miscarriage, Stillbirth, and Newborn Death. PLSP is For Fathers, Too. The Pregnancy Loss Support Program Is a community service of. The National Council of Jewish Women New York.
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Melinda Wilsford
Melinda Wilsford
3040 Pebble Road SE
Carrollton, OH, 44615-9574
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A Trisomy 18 Journey - Abigail Grace WilsfordDESCRIPTION
Story of a baby with a prenatal diagnosis of Trisomy 18 who lived 5 days. Includes Trisomy 18 and infant loss support resources.PARSED CONTENT
The domain trisomy18journey.org has the following on the web site, "If you have received a prenatal diagnosis of Trisomy 18." I analyzed that the webpage also said " Or another diagnosis that is incompatible with life, here you will find help in answering some of your questions." They also stated " What is Trisomy 18 Edwards syndrome? Is it better to carry to term or terminate. Where can I find help writing a birth plan. Where can I find stories. Of babies with trisomy 18? Where can I find support for pregnancy and infant loss. And for raising a child with Trisomy 18? How can God let this happen? Did you." The meta header had Trisomy 18 Trisomies trisomy18 Edwards syndrome Pictures Prenatal Diagnosis carrying to term infant death loss incompatible with life grief t18 photos pregnancy support as the first search term.SEE OTHER DOMAINS
Introduce yourselves and your pregnancy info. We are pregnant again! Newly Diagnosed with T18. Mother of a Newly Diagnosed T18 Baby.
Thank you to Hostaway for their ongoing support of this website. Here you will find much information on the rare chromosomal disorder, Trisomy 9p. There is information on a survey covering many different rare forms of Trisomy, photos of other children and links to support groups. I hope you all have much pleasure in browsing through the site and that some information can be of use to you.
Establishment, characterization, and differentiation of a karyotypically normal human embryonic stem cell line from a trisomy-affected embryo. Establishment, characterization, and differentiation of a karyotypically normal human embryonic stem cell line from a trisomy-affected embryo. Noninvasive method accurately and efficiently detects risk of Down syndrome. American Journal of Obstetrics and Gynecology.
Lilypie Angel and Memorial tickers. Tuesday, July 28, 2015. No bras were burned during this rally but it felt like it could have easily gone that way. My name is Elizabeth Arendale -. Once with my first child - as an unmarried scholarship soccer player in college. Why are we shocked? .
Trisomy Online is a free email based support group that was formed in 1997 for families and professionals whose lives have been touched by the diagnosis of a trisomy condition. Please join us in remembering all children who have died. We warmly invite all into this wonderful online community to share the ups and downs of life in the fun park, to gain the benefit .