ACDHO is very happy to announce the addition of another member!
We proudly welcome Stichting Hernia Diafragmatica, which is the world's first CDH charity and is based in The Netherlands!
http://www.chd.vuurwerk.nl/
https://www.facebook.com/pages/Stichting-Hernia-Diafragmatica/446008458744090
De Stichting Hernia Diafragmatica is opgericht in 1993
De doelstelling in het kort:
Steun geven aan hen die te maken hebben of krijgen met een KIND met een AANGEBOREN hernia diafragmatica.
Founded
in 1993, by a group of parents. The primary goals were to arrange for parents to meet each other
and to acquire knowledge about the disorder.
Welcome to the official web site of the Alliance of Congenital Diaphragmatic Hernia Organizations (ACDHO), an International group of professional charity and research organizations working together to better serve babies and families affected by Congenital Diaphragmatic Hernia.
Wednesday, November 20, 2013
Friday, November 1, 2013
CDH-New Zealand
ACDHO is very happy to announce the addition of another member!
We proudly welcome CDH-New Zealand, which is now supporting CDH families in New Zealand!
https://www.facebook.com/CDHNewZealand
This page has been created for parents and family members to share stories, gain info and keep in touch with anyone else that are or has been affected by CDH (Congenital Diaphragmatic Hernia) in New Zealand.
We proudly welcome CDH-New Zealand, which is now supporting CDH families in New Zealand!
https://www.facebook.com/CDHNewZealand
This page has been created for parents and family members to share stories, gain info and keep in touch with anyone else that are or has been affected by CDH (Congenital Diaphragmatic Hernia) in New Zealand.
HDC Hérnia Diafragmática Congenita Brasil
ACDHO is very happy to announce the addition of another member!
We proudly welcome HDC Hérnia Diafragmática Congenita Brasil, which is now supporting CDH families in Brazil!
We proudly welcome HDC Hérnia Diafragmática Congenita Brasil, which is now supporting CDH families in Brazil!
About
APOIE ESTA CAUSA!
Description
No início da gestação, quando o bebê ainda está se formando, existe um "buraco" no diafragma. Isto é normal, mas este "buraco" normalmente se fecha no terceiro mês de gestação. Isto acontece em cerca de 1 em cada 2.500 gestações. O fato dos órgãos abdominais terem subido até o tórax impede o desenvolvimento adequado dos pulmões, causando uma condição conhecida como hipoplasia pulmonar. Isto significa que os pulmões são menores do que eles deveriam ser.
Thursday, September 5, 2013
Olivia Faith Foundation, Inc
Meet Alliance of Congenital Diaphragmatic Hernia Organizations - ACDHO member, the Olivia Faith Foundation, Inc
A non-profit 501(c)3 Organization
- Raising global awareness for CDH
- Providing support to families affected by CDH and other conditions
- Awarding scholarships to students seeking a career in fetal therapy
- Aiding other organizations in research, prevention and treatments.
Olivia Faith was diagnosed with CDH at her 20 week ultrasound While still in the womb she survived a surgery that
would give her poorly developing lungs a chance to grow. She was born
on October 28, 2011 and had surgery to repair her diaphragm at 1 week
old. After 7 weeks in the NICU, with Mommy and Daddy by her side, she
passed into eternal life on December 18th 2011.
Visit their Facebook page at http://www.facebook.com/pages/Olivia-Faith-Foundation-Inc/48601600474466
Olivia Faith Foundation, Inc PO Box 690053 Vero Beach, FL 32969
DHREAMS Research Study (Congenital Diaphragmatic Hernia)
Meet Alliance of Congenital Diaphragmatic Hernia Organizations - ACDHO member, the DHREAMS Research Study (Congenital Diaphragmatic Hernia).
DHREAMS study was created to improve the understanding of the molecular genetic basis of CDH
Mission:
DHREAMS (Diaphragmatic Hernia Research & Exploration; Advancing Molecular Science) study was created to improve the understanding of the molecular genetic basis of CDH. This National Institute of Health (NIH)-funded research team is composed of health care providers and researchers across the country, coordinated at Columbia University Medical Center. Multiple medical centers are enrolling individuals and families with CDH. The knowledge gained through this research will lead to improved diagnosis, treatment, and quality of life for individuals and families with CDH.
Overview:
The DHREAMS study is an NIH funded multicenter national research study of congenital diaphragmatic hernia (CDH). The goal of our study is to improve the understanding of the causes of CDH.
General Information:
Each year more than 1,000 babies in the United States are born with a Congential Diaphragmatic Hernia (CDH). For the majority of these babies, the cause of the CDH is unknown.
Learn more at http://www.cdhgenetics.com/
Welcome
Welcome to the official web site of the Alliance of Congenital Diaphragmatic Hernia Organizations (ACDHO), an International
group of professional charity and research organizations working
together to better serve babies and families affected by Congenital
Diaphragmatic Hernia.
Labels:
ACDHO,
Alliance of Congenital Diaphragmatic Hernia Organizations,
CDH,
CDH Awareness,
CDH Charity,
CDH Foundation,
CDH Hospital,
CDH Research,
CDH Support,
Congenital Diaphragmatic Hernia
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