releases: http://upton.house.gov/news/documentsingle.aspx?DocumentID=362464
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| http://upton.house.gov/news/documentsingle.aspx?DocumentID=362464 | Bill to Help Children with Rare Diseases Like the Kennedy Girls of Mattawan Now One Step Closer to Becoming Law | 2013-11-21 | 2013 | 2013-11 | Republican | House | MI | Fred Upton | U000031 | upton.house.gov | legacy | House Energy and Commerce Committee Chairman Fred Upton, R-St. Joseph, joined House Speaker John Boehner, R-Ohio, as the Speaker signed S. 252, the PREEMIE Reauthorization Act, bringing the important bill one step closer to enactment. The bipartisan legislation also provides for the creation of the National Pediatric Research Network to facilitate research to help children with rare and genetic diseases. The House passed similar stand-alone legislation, H.R. 225, to create the network in February. Speaker Boehner also signed H.R. 3024, the Drug Quality and Security Act, a breakthrough bipartisan, bicameral agreement introduced by Upton to improve drug safety in the wake of the deadly 2012 meningitis outbreak. By all accounts, Michigan has been hardest hit by the outbreak with 264 cases and 19 fatalities, including 3 deaths from Upton’s own district. Upton’s committee has led a thorough investigation into the recent outbreak to ensure such a public health catastrophe never happens again. The bill also strengthens the prescription drug supply chain in order to protect American families against counterfeit drugs as well as eliminates needless government red tape that harms Michigan employers like Perrigo and Pfizer. Both bills will soon head to the President’s desk to be signed into law. Upton commented, “At long last we are nearing the finish line, and we will soon have a network in place to help families like the Kennedys in Mattawan, Michigan, and their two young daughters who have the rare disease Spinal Muscular Atrophy. These two little angels, Brooke and Brielle, are little warriors in the effort to boost research for rare diseases and serve as an inspiration for all.” IN CASE YOU MISSED IT ... November 14, 2013 Mattawan's Kennedy sisters help inspire House bill funding research into rare genetic diseases MATTAWAN, MI – The medical struggles of two sisters from Mattawan helped inspire a bill funding research for rare diseases that passed the House by unanimous consent this week. Brooke and Brielle Kennedy were born with type II spinal muscular atrophy. Their battle was chronicled in a 2012 Kalamazoo Gazette story. The six-year-old and four-year-old have exceeded doctors' prognoses, but SMA is a terminal, degenerative disease. "SMA is the leading genetic killer of infants and young children. It is a terminal, degenerative progressive disease that results in the loss of nerves in the spinal cord and the weakness of the muscles connected with those nerves," according to brookeandbrielle.com, a website set up by Sarah Kennedy, the girls' mother. "SMA impacts the ability to walk, stand, sit, eat, breathe and even swallow." U.S. Rep. Fred Upton, R-St. Joseph, introduced the National Pediatric Research Network Act of 2013, which passed Tuesday as part of the Prematurity Research Expansion and Education for Mothers who Deliver Infants Early (PREEMIE) Reauthorization Act. Upton sponsored the original PREEMIE act, which became law in 2006. The act supports research into rare and genetic diseases afflicting children, including SMA, by allowing the National Institutes of Health (NIH) to fund pediatric research consortium. Earlier this year, the measure passed the House as a stand-alone bill. "This legislation will have a dramatic and life-changing effect on so many families who have suffered for so many years," said Sarah Kennedy in a statement. Upton said he met the Kennedys a few years ago, when they brought to his attention to a similar bill written to help fund rare diseases affecting children. Upton said he was charmed by the girls and keeps a picture of them in his Kalamazoo office. "These girls are incredible. The first time I met Brielle and Brooke, they told me their names were Cinderella and Sleeping Beauty. They're not letting their disabilities define them. But because spinal muscular atrophy is relatively rare, there hasn't been a lot of funding for it," said Upton in an email. The bill will now move to the Senate as part of a package of health-related bills, S. 252. A previous version passed twice during the 112th Congress, once as a stand-alone bill and once as part of a larger piece of legislation. Neither version passed the Senate. "The sad reality is it is often difficult to conduct research into rare diseases due to the small number of individuals with the disease," he said. "We are working to change that and provide families with greater hope for a cure or advances in treatment." Read the entire story online here. Watch Upton’s November 12, 2013, floor statement that highlights the Kennedy family here. | 1 | 2026-03-30T12:14:52Z | 2026-03-30T12:14:52Z |