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CDH Research Patient Registry is a joint effort between CDH Patient Registry, DHREAMS and the CDH Study Group. If you have access, you may participate by filling out the Patient Registry questionnaire at https://cdhboards.org/survey/1 If you do not have access, or wish to get access, please click on "Participation" to the left.
You must be a member of CDH Patient Registry; patient must be a non-survivor or a survivor over 1 year of age. Sign up for free at CDH BOARDS . After you have joined, please e-mail [email protected] to gain access to the research survey.
Links to cdhresearch.org (8)
cdhboards.orgCDH Clubhouse - Congenital Diaphragmatic Hernia Support Group hosted by CDH International
cdhi.ukCDH International Registers as an NGO in the United Kingdom
cdhawarenessday.orgApril 19th is Global Congenital Diaphragmatic Hernia Awareness Day - CDH International - A Global Initiative to Stop Congenital
cdhresearch.comCDH International - A Global Initiative to Stop Congenital Diaphragmatic Hernia - The CDH Patient Registry is LIVE – Participate
cherubsuk.org.ukCDH International Registers as an NGO in the United Kingdom
cdhawarenessday.liveApril 19th is Global Congenital Diaphragmatic Hernia Awareness Day - CDH International - A Global Initiative to Stop Congenital