Peter Frampton, Rare Storyteller Peter Frampton, Rare Storyteller Inclusion Body Myositis Len Geiger, Rare Storyteller Alpha-1 Robyn, Deleon - Rare Storyteller Urea Cycle Disorder Rene & Rikki, Rare Storyteller Kabuki Syndrome Holly McNally Kabuki Syndrome Kyle Dempsey, Rare Storyteller Superficial Siderosis Taylor Schalk, Rare Storyteller Superior Mesenteric Artery Compression Cameron James, Rare Storyteller Atypical Hemolytic Uremic Syndrome (aHUS) Share on: Paul Braker, Rare Storyteller Autoimmune Encephalitis Harry Koujaian, Rare Storyteller Niemann Pick Type C (NPC) Share on: Claire Bevac, Rare Storyteller Auto Recessive Polycystic Kidney Disease and Congenital Hepatic Fibrosis (ARPKD/CHF) Adrienne Provost, Rare Storyteller Epidermolysis Bullosa Share on: Ryan Freund, Rare Storyteller MRX99 Share on: Matt O'Connell, Rare Storyteller Cystic Fibrosis Share on: Gene Andrasco, Rare Storyteller Hemiplegia of Childhood Todd and Corin Chapman, Rare Storytellers Peroxisomal Biogenesis Disorder Share on: Sarah Smith, Rare Storyteller Nemaline Myopathy Share on: Sue Rogers, Rare Storytellers Focal Segmental Glomerulosclerosis Share on: Sharon Rose, Rare Storyteller Klippel-Feil Syndrome Share on: Share on: Peter Dankelson, Rare Storytellers Peter Dankelson, Rare Storytellers Goldenhar Syndrome Share on: Sara Kennicott, Rare Storyteller Late Infantile Batten Disease Linda Bevec Auto Recessive Polycystic Kidney Disease/Congenital Hepatic Fibrosis Jess Ceisel, Rare Storyteller Undiagnosed and Rare Share on: Katie Thorstenson, Rare Storyteller Noonan Syndrome Stephen Mack, Rare Storyteller Joubert Syndrome Share on: Belle Banke, Rare Storyteller Belle Banke, Rare Storyteller Loeys-Dietz Syndrome