Airing weekdays at 7:30 A.M. on

Airing weekdays at 7:30 A.M. on

Imagine: A rare disease that’s rarely diagnosed because it mimics so many other diseases. We’re talking about Alpha-1 antitrypsin deficiency or AAT, a hereditary condition that may cause lung disease and liver disease. Dr. Kyle Hogarth, a pulmonologist at the University of Chicago, joins us to discuss the disease. Who’s at risk of getting this condition? What tests determine if you have it? And what lifestyle changes can help patients cope with this disease? We have lots of insight.

Health, Wealth, Beauty, and Business

Bringing the best tips from the experts in Atlanta in business, beauty, wealth management, child healthcare, car shopping, and more. Each year, Atlanta’s Women’s Entrepreneurship Initiative selects 15 local female entrepreneurs for a 15-month business training program. We meet women who have grown their companies, created jobs, and broke through the glass ceiling. With some […]

iMCD is the deadliest subtype of Castleman disease. Approximately one third of patients die within five years of diagnosis, and another third die within 10 years if not treated.

There are no effective treatment options for people with unresectable or metastatic chondrosarcoma despite many attempts by multiple pharmaceutical companies over the past few decades.

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