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Reps Eshoo, Ferguson, Sens Baldwin, Ernst Introduce Bipartisan, Bicameral Reform to Ensure Coverage for Children Born With Congenital Anomalies or Birth Defects

Drew Ferguson (R-GA) and Tammy Baldwin (D-WI) and Joni Ernst (R-IA) today reintroduced bipartisan, bicameral legislation to ensure health insurance coverage for needed treatment and procedures for individuals born with congenital anomalies or birth defects. The Ensuring Lasting Smiles Act would close a coverage gap to ensure that health plans cover medically necessary services related to a patient s anomaly or birth defect, including any serious dental and oral-related procedures that are necessary to maintaining health and overall function. Too many children born with congenital anomalies are denied coverage despite the long-term harm of such conditions. These are children like Rosie, the daughter of a family in my district who has congenital cataracts. She requires contact lenses because glasses aren t powerful enough, and without these lenses she is blind and will have no chance of ever developing normal vision, said

The Sturge-Weber Foundation Announces Molly Speer as a New Board of Director

Share: The Sturge-Weber Foundation (SWF) is honoured to announce Mrs. Molly Speer has joined the Board of Directors for the Sturge-Weber Foundation. Mrs. Speer is currently an Administrative Associate with Cummins, Inc in Greensburg, Indiana. She is also a graduate of Marion University. Mrs. Speer brings a commitment of service that will be highly beneficial to the SWF. Mrs. Speer has a daughter, Myla, who is diagnosed with Sturge-Weber syndrome. Myla has been an inspiration to the entire community and is honoured each year with a special event, Myla’s Mission, to raise critical funds for research and support. This year’s Myla’s Mission will take place in person and virtually on May 15, 2021 in Greensburg, IN.

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