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  1. Signatures
    554 out of 5,000
    Petitioning
    1. The President of the United States (+ 3 others)
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      • The President of the United States
      • The U.S. Senate
      • The U.S. House of Representatives
      • US Senate, House and President (United States Government)
  2. Created By
    Breath of Hope

RESOLUTION Designating March 31, as ‘National Congenital Diaphragmatic Hernia Awareness Day’.

Whereas the congenital diaphragmatic hernia birth defect is one of the most prevalent, lifethreatening birth defects in the United States;

Whereas the congenital diaphragmatic hernia birth defect is a severe, often deadly birth defect that has a devastating impact, in both human and economic terms, affecting equally people of all races, sexes, nationalities, geographic locations, and income levels; Whereas the congenital diaphragmatic hernia birth defect occurs in 1 in every 2,000 live births in the United States and accounts for 8 percent of all major congenital anomalies;

Whereas, in 2004, there were approximately 4,115,590 live births in the United States, and in approximately 1,800 of those live births, the congenital diaphragmatic hernia birth defect occurred, causing countless additional friends, loved ones, spouses, and caregivers to shoulder the physical, emotional, and financial burdens the congenital diaphragmatic hernia birth defect causes;

Whereas there is no genetic indicator or any other indicator available to predict the occurrence of the congenital diaphragmatic hernia birth defect, other than through the performance of an ultrasound during pregnancy;

Whereas there is no consistent treatment or cure for the congenital diaphragmatic hernia birth defect; Whereas the congenital diaphragmatic hernia birth defect is a leading cause of neonatal death in the United States;

Whereas 50 percent of the patients who do survive the congenital diaphragmatic hernia birth defect have residual health issues, resulting in a severe strain on pediatric medical resources and on the delivery of health care services in the United States; Whereas proactive diagnosis and the appropriate management and care of fetuses afflicted with the congenital diaphragmatic hernia birth defect minimize the incidence of emergency situations resulting from the birth defect and dramatically improve survival rates among people with the birth defect;

Whereas neonatal medical care is one of the most expensive types of medical care provided in the United States and patients with the congenital diaphragmatic hernia birth defect stay in intensive care for approximately 60 to 90 days, costing millions of dollars, utilizing blood from local blood banks, and requiring the most technically advanced medical care;

Whereas the congenital diaphragmatic hernia birth defect is a birth defect that causes damage to the lungs and the cardiovascular system;

Whereas patients with the congenital diaphragmatic hernia birth defect may have long-term health issues such as respiratory insufficiency, gastroesophageal reflux, poor growth, neurodevelopmental delay, behavior problems, hearing loss, hernia recurrence, and orthopedic deformities;

Whereas the severity of the symptoms and outcomes of the congenital diaphragmatic hernia birth defect and the limited public awareness of the birth defect cause many patients to receive substandard care, to forego regular visits to physicians, and not to receive good health or therapeutic management that would help avoid serious complications in the future, compromising the quality of life of those patients;

Whereas people suffering from chronic, life-threatening diseases and birth defects, similar to the congenital diaphragmatic hernia birth defect, and family members of those people are predisposed to depression and the resulting consequences of depression because of anxiety over the possible pain, suffering, and premature death that people with such diseases and birth defects may face;

Whereas the Senate and taxpayers of the United States want treatments and cures for disease and hope to see results from investments in research conducted by the National Institutes of Health and from initiatives such as the National Institutes of Health Roadmap to the Future;

Whereas the congenital diaphragmatic hernia birth defect is an example of how collaboration, technological innovation, scientific momentum, and public-private partnerships can generate therapeutic interventions that directly benefit the people and families suffering from the congenital diaphragmatic hernia birth defect;

Whereas collaboration, technological innovation, scientific momentum, and public-private partnerships can save billions of Federal dollars under Medicare, Medicaid, and other programs for therapies, and early intervention will increase survival rates among people suffering from the congenital diaphragmatic hernia birth defect;

Whereas improvements in diagnostic technology, the expansion of scientific knowledge, and better management of care for patients with the congenital diaphragmatic hernia birth defect already have increased survival rates in some cases;

Whereas there is still a need for more research and increased awareness of the congenital diaphragmatic hernia birth defect and for an increase in funding for that research in order to provide a better quality of life to survivors of the congenital diaphragmatic hernia birth defect, and more optimism for the families and health care professionals who work with children with the birth defect;

Whereas there are thousands of volunteers nationwide dedicated to expanding research, fostering public awareness and understanding, educating patients and their families about the congenital diaphragmatic hernia birth defect to improve their treatment and care, providing appropriate moral support, and encouraging people to become organ donors; and

Whereas volunteers engage in an annual national awareness event held on March 31, making that day an appropriate time to recognize National Congenital Diaphragmatic Hernia Awareness Day, Now,  Be It Resolved, 

That the Senate, House of Representatives and the President -  

(1) designates March 31, as ‘National Congenital Diaphragmatic Hernia Awareness Day’;

(2) supports the goals and ideals of a national day to raise public awareness and understanding of the congenital diaphragmatic hernia birth defect;

(3) recognizes the need for additional research into a cure for the congenital diaphragmatic hernia birth defect; and

(4) encourages the people of the United States and interested groups to support National Congenital Diaphragmatic Hernia Awareness Day through appropriate ceremonies and activities, to promote public awareness of the congenital diaphragmatic hernia birth defect, and to foster understanding of the impact of the disease on patients and their families.

Why People Are Signing
Recent Signatures

Pass a Resolution for March 31st to be CDH Awareness Day

Greetings,

Families of children with congenital diaphragmatic hernia, and adults with congenital diaphragmatic hernias are joining forces to have March 31st proclaimed as a Perpetual Congenital Diaphragmatic Hernia Awareness Day in the United States.

Since March 31, 2008 Congenital Diaphragmatic Hernia Awareness Day has been proclaimed by 35 States in the United States and many cities and counties in the U.S.

On April 14, 2010, the United States Sentate agreed to SR204 without amendment and with a preamble by Unanimous Consent a resolution designating March 31, 2010 National Congenital Diaphragmatic Hernia Awareness Day .

As residents, we are requesting that you help us reach our goal by sponsoring the attached Resolution declaring this special day in March.

A congenital diaphragmatic hernia birth defect occurs in 1 in 2,000 live births in the United States and accounts for 8% of all major congenital anomalies. With the rate of live births in the United States at 4,115,590 in 2004 (See, National Center for Health Statistics), this translates to approximately 1,800 live births with the congenital diaphragmatic hernia birth defect. Cystic Fibrosis occurs in 1 in 3,000 live births in the United States, and Spina Bifida has an occurrence of 7 in 10,000 or 1 in 1,478 live births. Currently, the general public has heard of both cystic fibrosis and spina bifida, although congenital diaphragmatic hernias occur just as often, with fatal results. Congenital Diaphragmatic Hernias are considered a “low profile” birth defect to the general public and have not received the attention and awareness needed.

To this day still approximately 50% of all cases result in death.

One of the most important advantages of prenatal diagnosis is the ability to anticipate a desperately ill newborn. “It is imperative that the mother be transferred to an appropriate perinatal center, where neonatal, ventilatory, and surgical expertise are available. This avoids the unnecessary mortality associated with transporting the sick neonate, and the delay in appropriate medical and ventilatory care that this entails." Fetal Ther 1987.

Since that day, I have been telling my story in an effort to raise awareness to the congenital diaphragmatic hernia birth defect. After finding little to no information or support, I joined forces with the organization, Breath of Hope, Inc., which is committed to supporting parents, children, family members and friends facing the diagnosis of a congenital diaphragmatic hernia birth defect.
I would be extremely honored if you would participate in sponsoring or co-sponsoring March 31 a special day to recognize people born with congenital diaphragmatic hernias, to remember loved ones who lost their battle with congenital diaphragmatic hernias, and to honor the dedicated health professionals who work with us.

A rough draft of what we imagine a Resolution would look like is available.

I would be most grateful if you could acknowledge my request as soon as possible so that we can make plans for promotion and celebration during the month of March. The United State’s participation in this event will have a profound impact on thousands of families and individuals. I thank you for your time and consideration.

Respectfully submitted,

[Your name]