{"version":"1.0","type":"rich","provider_name":"Acast","provider_url":"https://acast.com","height":250,"width":700,"html":"<iframe src=\"https://embed.acast.com/$/662171ead03d070012ca28fa/6a1886138fd07475b58bbf90?\" frameBorder=\"0\" width=\"700\" height=\"250\"></iframe>","title":"Left Behind","description":"<h2>Episode Summary</h2><p><br></p><p>What happens when the parade moves on, but you're still standing on the sidewalk? In this heavy and deeply candid episode of <strong>Breathless</strong>, host Jeremie Saunders addresses the modern paradox of the \"Trikafta Revolution.\" While a miraculous 90% of the Cystic Fibrosis community is experiencing a historical second chance at life, a remaining 10% is left stranded in the old world.</p><p>We follow the story of <strong>Teresa Weger</strong>, a 20-year-old university student from Weyburn, Saskatchewan. Teresa possesses an ultra-rare, spontaneous genetic mutation that places her entirely outside the reach of current modulator drugs. Jeremie pairs Teresa's current physical decline with his own history of severe CF complications, confronting the painful reality of survivor's guilt. This episode pulls back the curtain on the emotional isolation of being left behind by your own community, while exploring the cutting-edge genetics and future technologies—like mRNA and CRISPR—needed to finish the fight for everyone.</p><p><br></p><h2><br></h2><h2>Main Topics &amp; Key Moments</h2><p><br></p><p><br></p><h3>1. The Meshed Reality of a Revolution</h3><ul><li><strong>The Shrinking Base:</strong> Teresa Weger notes a drastic shift in the CF community. As health dramatically improves for the majority, community enthusiasm and attendance at advocacy events (like local walks) have noticeably waned.</li><li><strong>Tempered Joy:</strong> CF Canada CEO <strong>Kelly Grover</strong> notes that while reaching \"first base\" is a biological triumph, the organization's celebrations must remain tempered until therapeutic options exist for 100% of patients.</li></ul><h3>2. The Genetic Lottery &amp; Spontaneous Mutation</h3><ul><li><strong>The \"Toyota Camry\" vs. The Custom Model:</strong> The vast majority of CF patients carry the common Delta F508 mutation. Teresa's mutation is an ultra-rare, complex anomaly: <strong>W57X/exon 23-24 deletion</strong>.</li><li><strong>The Biological Glitch:</strong> Chief Scientific Officer <strong>Dr. Paul Eckford</strong> explains a rare break from the classic inheritance model. While Teresa's mother is a standard carrier, her father is not. Teresa’s CF was caused by a completely spontaneous, random genetic mutation during DNA replication at the exact moment of conception.</li></ul><h3>3. The Physical Toll of the Old World</h3><ul><li><strong>The Linear Decline:</strong> After maintaining a stable childhood with a lung function of 97%, Teresa experienced a sudden adolescent crash, with her lung capacity dropping into the 50s.</li><li><strong>The Multi-Front War:</strong> A graphic look at severe CF symptoms outside the lungs, highlighting Teresa’s struggles with chronic gastrointestinal blockages and painful sinus surgeries that result in post-sedation complications.</li></ul><h3>4. Isolation at the Parade</h3><ul><li><strong>The Regina CF Walk:</strong> Teresa recalls the painful emotional whiplash of standing backstage at a fundraising walk. Ahead of her, a Trikafta-responsive speaker joyfully proclaimed that her sweat chloride levels had normalized to healthy standards—leaving Teresa to follow with a speech detailing her rapid physical decline.</li><li><strong>Parallel Tracks, Forked Roads:</strong> Jeremie recognizes his own past medical trauma in Teresa’s current daily fight—specifically their shared history of aggressive sinus polyps and major large intestine resections 75% of Jeremie's large bowel was removed). He struggles to navigate the raw survivor's guilt of receiving a \"golden ticket\" while others remain waiting.</li></ul><h3><br></h3><h2>Key Quotes</h2><ul><li><em>\"The experience of feeling like you're on the same team but no longer working for the same goal... we all still have CF, but they don't still have the same CF as me.\"</em> — <strong>Teresa Weger</strong></li><li><em>\"It's like winning the lottery, only the prize is a life-limiting genetic disease that no pharmaceutical company has built a drug for because you might be the only person on earth with your specific genetic code.\"</em> — <strong>Host (Jeremie)</strong></li><li><em>\"I am the one who got to keep living. And she is the one who is still waiting.\"</em> — <strong>Host (Jeremie)</strong></li><li><em>\"We aren't done. And we won't be done until the bus stops for everyone.\"</em> — <strong>Host (Jeremie)</strong></li></ul>","author_name":"Snack Labs"}