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Website: https://www.kararyska.com/
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Effisode - Shake It Off
A Rare Collection - Underestimated
Rare Friends Forever - Hanging Out and Showing Some Love to Brene Brown with Katie Lloyd and Adam Johnson
Effisode - Inclusion Revolution
Rare Disease Families Have Plenty of Hope - What They Need is Help. Transforming Drug Development w/ NF2 Biosolutions, Nicole Henwood & Vibe Bio, Alok Tayi
Together We Can Cure Single-Gene Disorders Starting with PGAP3 - Moonshot - An Ambitious and Innovative Project with Geri and Zach Landman
Effisode - Montana or Bust
Rare Disease Siblings, The Glass House Children - Bulletproof and Shattered - With SMA Sibling Cara Freedman
A Rare Collection - Easier Said Than Done
Effisode - The Lunchboxes
When Your Career and Personal Life Collide - VP of Medical and Science Strategy and Head of Syneos Health's Rare Disease Consortium FSHD Rare Dad - Raymond Huml
Ensuring that the Patient and Caregiver Voice are Part of Clinical Trial Design and Engagement - Bridging the Gap with Industry with Shazia Ahmad
Effisode - CTNNB1 Awareness Day - Rare Disease Family Meet-Up
Summer Surfing - Get On Top of the IEP Wave - Things You Can Do This Summer to Make Next Year Better with Gay Grossman
A Rare Collection - I Will Never Forget
Effisode - Back on Track - All Aboard the Inclusion Train
Half of the Day She's a Diversity Champion, the Other Half a Rare Disease Mom and Caregiver with Yosr Hamza
A Rare Mama Bear - Being a Single Parent and Adopting a Rare Disease Child with Epidermolysis Bullosa
Effisode - Global Genes RARE Disease Patient Advocacy Summit
Picking the Brain of a Rare Disease Dad - With CTNNB1 Dadvocate - Casey Parks
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It is Free
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Uncanny
Dead Eyes