Renowned Nutrition Expert Puts Rare Disease Day on the Radar
Dr. Virginia A. Stallings Discusses Individualized Nutrition Therapy for People with Cystic Fibrosis
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Virginia A. Stallings, M.D., highlights the nutritional challenges and therapies for people living with one of those rare diseases, cystic fibrosis (CF). An in-depth discussion/presentation by Dr. Stallings, entitled, Individualized Nutrition Therapy For People With Cystic Fibrosis: Gaining Or Losing Weight, will be featured on the Cystic Fibrosis Research Inc. (CFRI) podcast,
Rare Disease Day, held annually on the final day of February, recognizes the 6,000+ rare diseases worldwide, 72 percent of which are genetic. More than 300 million people live with a rare disease across the globe. There are 30,000 people in the U.S. and 70,000 worldwide diagnosed with cystic fibrosis, managing its many debilitating effects on the respiratory and digestive systems.
Renowned Nutrition Expert Puts Rare Disease Day on the Radar
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Renowned Nutrition Expert Puts Rare Disease Day on the Radar
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Claire’s Place Foundation Expands COVID-19 Programs to Support People with Cystic Fibrosis
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Non-profit reflects on trying year for the cystic fibrosis community & looks ahead to 2021. I feel this program is perhaps the best way to empower the CF community,” said Work Proudly Program Participant Derek. “I ve never heard about a CF program like this. The team at Claire’s Place Foundation are trailblazers. LOS ANGELES (PRWEB) December 17, 2020
Claire’s Place Foundation, a non-profit organization providing support to children and families affected by cystic fibrosis (CF), is pleased to announce that its COVID-19 Emergency Fund and new Work Proudly Program have had a significant impact assisting the CF community through the pandemic and will expand in 2021. The fund provided essential needs to people with CF throughout the COVID-19 outbreak, while the Work Proudly Program is supporting the com