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Illinois and Vermont have joined 37 other states and the District of Columbia in requiring that all newborns be screened for cystic fibrosis at birth.
In addition, the Nevada Department of Health has decided to begin regular CF screening as well. Routine screening will be implemented when state lawmakers set an implementation date.
"Early diagnosis for cystic fibrosis is critically important because it gives every newborn a better chance for better health and a longer life," said Robert J. Beall, Ph.D., president and CEO of the Cystic Fibrosis Foundation. "We congratulate the 40 states in the country who are now screening for the disease, and look forward to every state in the union joining this important effort."
Cystic fibrosis is a fatal genetic disease that affects 30,000 children and adults in the United States. Newborn screening for cystic fibrosis is important because more than 10 million Americans are symptomless carriers of a cystic fibrosis gene. Additionally, most people who have a child with CF are not aware of a family history of the disease. Cystic fibrosis causes thick mucus to build up in the lungs and other organs, resulting in life-threatening infections and serious digestive complications.
Research studies show that newborn screening for CF will likely improve and extend the lives of those born with the disease. Early diagnosis allows affected infants to begin therapeutic interventions immediately. In research studies, these interventions have been shown to improve height, weight, nutrition, cognitive and lung functioning, and to reduce hospitalizations.
When the Cystic Fibrosis Foundation was created in 1955, few children lived to attend elementary school. Today, as a result of dramatic improvements in research and care, the median age of survival for a person with CF is 37 years. The Cystic Fibrosis Foundation strongly urges all states to implement comprehensive programs for routine newborn screening for cystic fibrosis.
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In addition, the Nevada Department of Health has decided to begin regular CF screening as well. Routine screening will be implemented when state lawmakers set an implementation date.
"Early diagnosis for cystic fibrosis is critically important because it gives every newborn a better chance for better health and a longer life," said Robert J. Beall, Ph.D., president and CEO of the Cystic Fibrosis Foundation. "We congratulate the 40 states in the country who are now screening for the disease, and look forward to every state in the union joining this important effort."
Cystic fibrosis is a fatal genetic disease that affects 30,000 children and adults in the United States. Newborn screening for cystic fibrosis is important because more than 10 million Americans are symptomless carriers of a cystic fibrosis gene. Additionally, most people who have a child with CF are not aware of a family history of the disease. Cystic fibrosis causes thick mucus to build up in the lungs and other organs, resulting in life-threatening infections and serious digestive complications.
Research studies show that newborn screening for CF will likely improve and extend the lives of those born with the disease. Early diagnosis allows affected infants to begin therapeutic interventions immediately. In research studies, these interventions have been shown to improve height, weight, nutrition, cognitive and lung functioning, and to reduce hospitalizations.
When the Cystic Fibrosis Foundation was created in 1955, few children lived to attend elementary school. Today, as a result of dramatic improvements in research and care, the median age of survival for a person with CF is 37 years. The Cystic Fibrosis Foundation strongly urges all states to implement comprehensive programs for routine newborn screening for cystic fibrosis.
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