Airing weekdays at 7:30 A.M. on

Airing weekdays at 7:30 A.M. on

Cystic Fibrosis affects people from all walks of life and all age groups. One American company has dedicated itself to meeting the demands of Cystic Fibrosis patients bringing a whole level of care to this debilitating disease. Tune-in as The Balancing Act host Julie Moran sits down with Foundation Care co-founders, Dan Blakeley and Mike Schultz, in this “Behind the Mystery: Rare and Genetic Diseases” segment. If you suffer with Cystic Fibrosis or know someone who does, you’re urged to watch this informative Lifetime Television show.

The National Organization for Rare Disorders (NORD®) is celebrating Rare Disease Day 2021 with The Balancing Act.

Travis Flores is a 29-year-old cystic fibrosis survivor and a recipient of a very rare third double-lung transplant in May 2020.

The Balancing Act has partnered with the National Organization for Rare Disorders (NORD) and WEGO Health to shine a light on rare diseases and the impact they have on patients.

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