On Rare

At 27, Gwyn is a college student pursuing a career as a dietitian and the host of A Little View, a podcast that creates space for candid conversations within the dwarfism community and beyond. Her interests are deeply informed by her own experiences growing up with achondroplasia, including challenges with body image, an eating disorder, and feeling misunderstood by healthcare providers. In this episode of On Rare, David Rintell, Head of Patient Advocacy at BridgeBio, and Mandy Rohrig, Vice President of Patient Advocacy at BridgeBio, speak with Gwyn about learning to embrace her condition, finding strength and connection through community, and turning some of her most difficult experiences into opportunities to help others. She reflects on the importance of shared experience, speaking openly about difficult topics, and supporting people in making the choices that are right for them.

Michelle Norton, Senior Director of Clinical Science at BridgeBio Skeletal Dysplasia, provides a medical overview of achondroplasia. Achondroplasia is a rare genetic condition that affects bone growth and is the most common cause of disproportionate short stature skeletal dysplasia. It is caused by a genetic change in the FGFR3 gene, which regulates bone growth, and approximately 80% of people with achondroplasia are born to average-stature parents as the result of a spontaneous genetic change. Michelle also explains that achondroplasia is about more than height, as people may experience complications including sleep apnea, frequent ear infections, and orthopedic and spinal issues, while emphasizing that each person’s experience with the condition is unique.

In this episode of On Rare: Innovators, David Rintell and Mandy Rohrig of BridgeBio, speak with physician, scientist, and drug developer Stan Crooke. Stan is the founder of the n-Lorem Foundation, a nonprofit focused on developing individualized medicines for people living with nano-rare genetic conditions and providing those medicines for life. Stan reflects on the experiences that shaped his career, from discovering his passion for science and medicine to pioneering antisense technology.  He is motivated by the responsibility that comes with having the knowledge and tools to help people whose conditions are too rare for traditional drug development.

Stan shares how conversations with families seeking options for their children led him to establish n-Lorem and shift his focus from developing medicines for millions of people to working “one patient at a time.” He discusses the science behind antisense oligonucleotides, the impact nano-rare conditions can have on entire families, and why he sees the opportunity to continue learning and working on behalf of patients as a privilege. For Stan, innovation is rooted in curiosity, empathy, and a willingness to act when you know you can make a difference.

Looking back on a career devoted to drug development, Stan describes himself simply as a worker, scientist, and physician, but by the end of the conversation, he offers another description: a “dream merchant,” someone who has had the opportunity to dream of health and wellbeing for others and work to make those dreams possible.

Severe high blood pressure and an unexplained feeling of heaviness led Adrienne to the emergency room at age 26, where scans revealed cysts throughout her kidneys and ultimately led to a diagnosis of autosomal dominant polycystic kidney disease (ADPKD). With no family history of the condition, Adrienne learned that her ADPKD was caused by a spontaneous genetic mutation.
In this episode of On Rare, David Rintell, Head of Patient Advocacy at BridgeBio, and Mandy Rohrig, Vice President of Patient Advocacy at BridgeBio, speak with Adrienne about navigating the uncertainty of a new diagnosis, recurrent hypertensive crises, and the discovery of brain aneurysms that eventually required a craniotomy. Adrienne also shares how finding the PKD community helped her feel less alone and inspired her to become a mentor, advocate, and patient voice in research and policy.
Nile Abularrage, Senior Director of Business Development and Operations at GondolaBio, provides a scientific overview of ADPKD. ADPKD is a genetic condition that causes fluid-filled cysts to progressively grow in the kidneys, which can enlarge the kidneys and lead to pain, high blood pressure, and declining kidney function over time. While ADPKD is most often inherited from a parent, it can also result from a spontaneous genetic mutation, as it did for Adrienne. Nile also explains how ADPKD can affect other parts of the body, including an increased risk of intracranial aneurysms and cysts in the liver. While treatment options remain limited, he shares why this is an exciting time for ADPKD research, with growing interest and a number of promising approaches being explored for the community.

Excruciating pain after even brief sun exposure, years without answers, and a life-threatening liver crisis shaped Ashley's journey with erythropoietic protoporphyria (EPP), a rare genetic condition that causes severe photosensitivity. Although Ashley experienced symptoms beginning in early childhood, she wasn't diagnosed until after her 40th birthday, when she was hospitalized with advanced liver disease ultimately requiring a transplant. In this episode of On Rare, David Rintell, Head of Patient Advocacy at BridgeBio, and Mandy Rohrig, Vice President of Patient Advocacy at BridgeBio, speak with Ashley about her decades-long diagnostic journey, the emotional experience of waiting for a donor organ, and how finding a physician living with porphyria finally led to answers. Ashley reflects on the challenges of living in the shadows to avoid sunlight, navigating life after transplant, and why sharing her story has become one of her greatest purposes. 

Dr. Pete Schmidt, Chief Medical Officer of GondolaBio provides a medical overview of EPP and X-linked protoporphyria (XLP). Both conditions are rare genetic disorders caused by the buildup of protoporphyrin IX, a molecule that becomes highly reactive when exposed to visible light. This reaction causes severe pain and inflammation in the skin after sun exposure and, in some people, can lead to progressive liver damage as protoporphyrin accumulates in the liver and bile ducts. Dr. Schmidt explains the underlying biology of EPP, why symptoms can be difficult to diagnose, and the challenges of managing both the painful photosensitivity and the risk of liver disease.

Severe seizures, nonstop crying, and an exaggerated startle reflex marked the beginning of Elliott’s journey with molybdenum cofactor deficiency type A (MOCD type A), an ultra-rare inherited metabolic disorder that can cause devastating neurological damage shortly after birth. After initially being told that Elliott would likely not survive to school age, his family was offered access to an experimental treatment that changed the course of his life. In this episode of On Rare, David Rintell, Head of Patient Advocacy at BridgeBio, and Mandy Rohrig, Senior Director of Patient Advocacy at BridgeBio, travel to England to meet Elliott and his family and hear how they navigated diagnosis, uncertainty, and hope after already experiencing the heartbreaking loss of another child. Geoff and Lucy, Elliott’s parents, reflect on the emotional toll of diagnosis, the realities of managing complex medical care at home, and the joy of watching Elliott grow, attend mainstream school, and live life alongside his siblings. Their story highlights the importance of early diagnosis, caregiver resilience, and the life-changing impact of treatment for rare disease families.

Dr. Günter Schwarz, Professor of Biochemistry at the University of Cologne and a leading expert in MOCD, provides a medical overview of the condition. MOCD is a rare inherited metabolic disorder caused by the body’s inability to produce molybdenum cofactor, which is required for several critical enzymes to function properly. Without it, toxic sulfite builds up in the body, particularly in the brain, leading to severe seizures, neurological injury, and often early death. Dr. Schwarz explains how the condition is inherited, why symptoms begin so early in life, and how targeted treatment can dramatically alter outcomes when started quickly after diagnosis.