NOTE: On June 19-20, the Children's Hospital Association will be holding our ninth annual Family Advocacy Day in Washington, DC. Leading up to the event, we'll be posting stories by the amazing moms and dads of some of our attending children. Today's story is about Sydney Mayrell by her mom, Erin.
NOTE: On June 19-20, the Children's Hospital Association will be holding our ninth annual Family Advocacy Day in Washington, DC. Leading up to the event, we'll be posting stories by the amazing moms and dads of some of our attending children. Today's story is about Riley Cerabona, by her mom, Kristen Davis.
NOTE: On June 19-20, the Children's Hospital Association will be holding our ninth annual Family Advocacy Day in Washington, DC. Over the next month, we'll be posting stories by the amazing moms and dads of some of our attending children. Today's story is about Victoria Everett by her mom, Carye.
On May 1, Children’s Hospital Association CEO Mark Wietecha spoke at The Atlantic Health Care Forum in Washington, D.C., which featured speakers and panels on a range of health care topics.
On May 2, the Association, in cooperation with the Children’s Health Care Caucus, hosted its second briefing, “CHIP 101: Past, Present and Future,” in the four-part Medicaid Matters for Kids series.
A quick (and simplified) refresher on how the federal budget process is supposed to work:
LaKeesha Hines and her son, Braelyn, represented St. Joseph’s Children’s Hospital in Tampa, FL, at our 2010 Family Advocacy Day. Braelyn, who was born healthy but contracted bacterial meningitis as an infant, had been under St. Joseph’s Children’s care nearly his entire life at the time he attended Family Advocacy Day. Medicaid has covered a significant portion of the intensive care he requires. LaKeesha graciously shares what Medicaid has meant to Braelyn’s recovery and well-being.
On Feb. 22, the Children’s Hospital Association kicked-off its four-part Medicaid Matters for Kids briefing series with Medicaid and Kids 101. The briefing gave congressional staff a “101,” or basic understanding, of Medicaid’s structure, including: who the program serves, what types of services it provides, and how it is financed.
Simone spent more than a year in the hospital after her birth and has had many more visits since due to various illnesses and for surgeries due to craniosynostosis, a skull deformity; tracheomalasia, a floppy airway; and cystic fibrosis (CF), a chronic lung disease. Because of her fragile lung status, she has a tracheostomy (a surgically created opening in the neck leading directly to the trachea) and requires oxygen and mechanical ventilation at night. Last January, Simone suffered a severe stroke during surgery and was paralyzed on her right side. With the help of therapists at Mt. Washington Pediatric Hospital, Simone has regained most of what she lost. We were honored to have her join us for Family Advocacy Day in 2012, and recently reached out to her mother, Shannon, for an update as part of our Medicaid Matters for Kids Month.
It’s likely that if you’re reading this blog, you already understand the importance of Medicaid to our nation’s children. We like to toss around numbers and statistics when we talk about the program – such as the fact that more than one in three children in the United States is covered by Medicaid – but eventually numbers start to lose meaning. In June of 2011, over 27 million non-disabled children were enrolled in Medicaid. When you add in disabled children, the number of children enrolled in Medicaid is 32 million.