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This weeks guest Madeline Weiss she was born with a rare genetic lung disease called Primary Cillary disease. She wasn’t diagnosed with it until she was 13 years old. She shares her story of growing up with this condition and how it affects her daily life. She discusses how her love of music and theatre has helped her cope with her daily challenges. She also shares how the pandemic has affected her life while dealing with a lung disease.
By disabilitytoabilityThis weeks guest Madeline Weiss she was born with a rare genetic lung disease called Primary Cillary disease. She wasn’t diagnosed with it until she was 13 years old. She shares her story of growing up with this condition and how it affects her daily life. She discusses how her love of music and theatre has helped her cope with her daily challenges. She also shares how the pandemic has affected her life while dealing with a lung disease.