Often times families in the midst of early grief do not realize that there are national support organizations that deal with very specific genetic or fetal anamoly issues. If you know of organizations that were helpful to you or someone you know, please share some here. For example:
http://www.trisomy18.org/site/PageServer
http://www.marchofdimes.com/mission/prematurity.html
http://www.cjsids.org/
http://www.ndss.org/
http://www.americanpregnancy.org/pregnancycomplications/miscarriage.html
Is this blog still active? Not just this topic (this is the only place i could find to try to ask a question). If it is, could you please post a new topic, anything, to show its still active? I would like to take part if anyone still looks at this blog page.
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