Susannah Cahalan and her Month of Madness

September 6, 2019

Journalist and best-selling author Susannah Cahalan, ahead of her keynote address at the Global Genes RARE Patient Advocacy Summit September 18 in San Diego, discusses her diagnostic odyssey, the critical role the support of her loved ones made, and what allowed the doctor who diagnosed and treated her to succeed where others had failed.rare disease diagnositic odyssey

Stay Connected

Facebook Twitter Instagram Youtube

Susannah Cahalan and her Month of Madness

Related

What Being Undiagnosed Means in the Rare Community

Sharing Fibrodysplasia Ossificans Progressiva Stories During Global FOP Awareness Day

Journey to a Diagnosis for Kabuki Syndrome

Recognizing the Intersection of Stress and Hope

To Walk A Mile In My Shoes

The Making of MOGAD Awareness Month and the Creation of “The Flock”

Bohring-Opitz Syndrome Diagnosis Drives Mother’s Advocacy

Patient Journey with Multiple Rare Diagnoses: “This. Isn’t. My. Body.”

A Girl Who Never Gave Up Despite Trigeminal Neuralgia Diagnosis

Stay Connected