Scientific Director Tanya Brown shares her story of growing in confidence as a scientist, inspired by her mother's resilience and perseverance.
Read More"Answering the Shrug," by Yssa DeWoody
When a doctor offers only a shrug in response to her daughter’s exam, Yssa DeWoody sets off on her path to becoming an advocate.
Read More"Reason to Hope," by Melissa Chaikof
When Melissa Chaikof receives first learns that her daughters are profoundly deaf and then, when they are older, that they are also going blind, she cannot sit back and wait for others to find a cure.
Read More"The Power of Finding Your Community," by Tracy Milne
When Tracy Milne's young son is diagnosed with a rare disease, she finds hope in community.
Read More"The Day My World Changed," by Maddison Hall
After dreams of a perfect parenthood, Maddison was thrown into the rare disease world and became an unexpected advocate for her daughter and others in the Glut1 Deficiency Community.
Read More"Can We Fix It?" by Kasha Morris
This is a story about fixing an impossible problem in an unexpected way.
Read More"What's Wrong With My Baby?" by Julie Raskin
Julie Raskin recalls her son's birth and strange variation of nursing and sleep of the first two days of his life.
Read More"That 'Spinning Room' Moment," by Jill Kiernan
This is a story about one family's rare disease journey and the birth of a community.
Read More"Driving Miss Dorie," by Dorie Shapiro
Prepare to be entertained by the thrilling saga of Dorie's fearless teenage driving escapades!
Read More"Super Bowl Sunday: Diagnosis Day," by Erin Coller
After a year of seeking answers and a diagnosis for her toddler son’s delays and seizure, Erin Coller shares how, one Super Bowl Sunday, a phone call from the neurologist changed their lives forever.
Read More"Wrestling with an Estranged Father's Legacy," by Jeff Levenson
In an unexpected twist of where he thought his life would take him, Jeff finds one of his greatest purposes in life raising awareness of and helping find therapies for rare diseases.
Read More"Heart vs. Brain," by Cassi Friday
A scientist used to compartmentalize as a way of emotional preservation but learned to harness the anxiety that comes with being a rare disease caregiver to help patients with her children's rare disease.
Read More"The Journey Is Just Beginning," by Carmen Camacho
Carmen Camacho's story spans decades, but her journey is just beginning.
Read More"Navigating a World Not Built for Us," by Avery Roberts
Avery Roberts is breaking down barriers tackling misconceptions surrounding disability and giving a loud voice to the, often-forgotten, rare disease community.
Read More"How My Bad Dating History Led to Me Being a Rare Disease Advocate," by Becky Nieves
Do you know what happens when a Type A fixer turns into a rare disease mom warrior? Then have a listen!
Read More"Strong," by Amber Black
A mother's journey with self-identity while navigating her two-year-old son's rare genetic epilepsy.
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