Congenital diaphragmatic hernia (CDH) was first described in 1679 by Lazarus Riverius who incidentally noted a CDH on a postmortem examination in a 24 year old.
Citation: The CDH study group and advances in the clinical care of the patient with congenital diaphragmatic hernia Nora M Doyle, Kevin P Lally Seminars in Perinatology - June 2004 (Vol. 28, Issue 3, Pages 174-184, DOI: 10.1053/j.semperi.2004.03.009)
In 1701, Sir Charles Holt described the classical clinical and postmortem findings of an infant with CDH in philosophical transactions of the Royal Society of London.
Citation: Weblink here
Updated: Jun 12, 2009
In 1848, Victor Alexander Bochdalek, a professor of anatomy in Prague described both right and left posterolateral CDH. To this day, CDH commonly is referred to as a Bochdalek hernia in honor of Victor Bochdalek's contribution to this field. Citation: Weblink here
Not to dispute the findings and severe health crisis which HIV and AIDS has presented in this world, but in the last 20 years, the advances of care and maintaining health for those affected by HIV has evolved not to be a death sentence. First reported in the 1980s in the United States Citation Here: WebLink here
Congenital Diaphragmatic Hernia (CDH) has been reported, studied, evaluated, researched for the last 300 years and still to about 50% of those diagnosed overall it is a death sentence? A death sentence before their 1st birthday.
Everyone is aware of HIV, even those who have never directly encountered it. Not everyone is aware of CDH, only those who have directly encountered it. This needs to change.
The only way this can change is if we make our Government officials and the general public aware that CDH has been reported, diagnosed and treated for 300 years but no one is aware. If you would like to make your local, state or federal Representatives aware, educate the general public, take a hour of your time and write them. Request a sample letter and proclamation/resolution by contacting us at firstname.lastname@example.org, we will gladly send you the documents to do this.
Only when they are aware, when the general public becomes more aware will there be more research in order to bring the survival rates higher. When more are aware they will fund medical research for this birth defect. More will realize that survivors of CDH need specialized care and therapies early in order for these children to maintain health. Until we start with the first step, no one will listen. The first step is our elected officials and the general public.
It just is not acceptable for 300 years, CDH has been documented and the survival rates are still over all at 50%.
"Never doubt that a small group of thoughtful, committed people can change the world. Indeed, it is the only thing that ever has." - Margaret Mead