Once Upon A Gene
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What is Chronically Surviving with Marcelle Longlade
33 mins; September 17, 2020
Ciitizen - Take Control of Your Own Medical Records and Advance Research with Nasha Fitter
30 mins; September 10, 2020
School Busses, Road Trips and Friendship
4 mins; September 08, 2020
A Family Plagued with Rare Genetic Disease, Adrenoleukodystrophy with Diane Kane
27 mins; September 03, 2020
Two Disabled Dudes - Kyle Bryant and Sean Baumstark
36 mins; August 27, 2020
Rare Together, Watch Together - Film Selections from The Disorder Channel in Partnership with Global Genes
27 mins; August 26, 2020
Effisode - Let Me Tell You About My Big Brother
4 mins; August 25, 2020
A Mother's Crusade to Find a Cure for Her Son - Amber Freed, Founder and CEO, SLC6A1 Connect
42 mins; August 20, 2020
David Fajgenbaum - Chasing My Cure - A Doctor's Race to Turn Hope into Action
53 mins; August 13, 2020
Effisode 001
7 mins; August 11, 2020
WSU ROAR - Responsibility, Opportunities, Advocacy and Respect with Lisa Henniger
30 mins; August 06, 2020
Time is Brain - SynGap Research Fund with Mike Graglia
35 mins; July 30, 2020
Bonus Episode - Usher Syndrome Type III with Eleanor Griffith from Grey Genetics
54 mins; July 27, 2020
Physical and Emotional Well-Being for the Caregiver with Tyra Skibington
46 mins; July 23, 2020
Next Steps - A Journey Through CRPS to an Above the Knee Amputee with Whitney Lavender
34 mins; July 16, 2020
Rare Like Us with Taylor Kane
37 mins; July 09, 2020
Founder of LakiKid - Sensory Tools for Home and Classroom with Jason Hsieh
28 mins; July 02, 2020
Anna Laurent on Alagille Syndrome and Her Road to Advocacy
38 mins; June 25, 2020
Sage Graves - Estate Planning, Guardianship, Special Needs Trusts
38 mins; June 18, 2020
The Ladies Behind the Edits
34 mins; June 11, 2020
Loving Large: A Mother's Rare Disease Memoir With Patty Hall
41 mins; June 08, 2020
In Loving Memory of Lucas DeFabio
4 mins; June 06, 2020
Beyond Quarantine: Acceptance, Empathy, and a Better Normal
35 mins; May 28, 2020
Quarantine - What We're Missing, What We're Not, and What We Hope Sticks Around
31 mins; May 21, 2020
Trust Your Instincts; An Early Intervention Can Save Your Life
37 mins; May 14, 2020
Put Your Own Oxygen Mask On First
30 mins; May 07, 2020
Rare Disease Trailblazer and Co-Founder of Disorder - The Rare Disease Film Festival
36 mins; April 30, 2020
Therapy Check-In With Rose Reif
38 mins; April 23, 2020
How Our Rare Kids Can Shape Us
34 mins; April 16, 2020
A Grandfather's Story of Guardianship, Caregiving and Advocacy
42 mins; April 09, 2020
Choosing Hope
33 mins; April 02, 2020
Mental Health and Coping During Covid-19
38 mins; March 26, 2020
School Closures and FAPE
28 mins; March 19, 2020
A Healthier Healthcare For All
40 mins; March 12, 2020
Morgan's Wonderland
27 mins; March 05, 2020
Neena Nizar and the Jansen's Foundation
37 mins; February 27, 2020
Distressed Genes Aren't Just A Fashion Statement
41 mins; February 20, 2020
The Value of Genetic Counselors
45 mins; February 13, 2020
The Lucky Few
25 mins; February 06, 2020
Films and Fatherhood
38 mins; January 30, 2020
A Fellow CTNNB1 Mama
24 mins; January 23, 2020
Sibling Support
35 mins; January 16, 2020
My Favorite Pair of Genes
9 mins; January 09, 2020
Rollin' With Spina Bifida
40 mins; January 02, 2020
My Pfieffer Pfamily
33 mins; December 26, 2019
The Fathers Network
45 mins; December 19, 2019
Heartism
48 mins; December 12, 2019
A Little Love
26 mins; December 05, 2019
The Dadurday Chronicles
32 mins; November 28, 2019
It's Your Party, and I'll Cry If I Want To
32 mins; November 21, 2019
Telomere More About It
27 mins; November 14, 2019
Hospital Hair Don't Care
26 mins; November 07, 2019
Effie
13 mins; October 28, 2019
Effie and Synthiea
21 mins; October 28, 2019
Trailer
3 mins; October 28, 2019