{"podcast":{"title":"All Access DNA","slug":"all-access-dna-7139504","podcast_index_feed_id":7139504,"rss_url":"https://feed.podbean.com/allaccessdna/feed.xml","website_url":"https://allaccessdna.podbean.com","image_url":"https://pbcdn1.podbean.com/imglogo/image-logo/19769156/Podcast_App_Logo6mapx.jpg","author":"allaccessdna","episode_count":67,"summary":"What is DNA anyway? Should I consider genetic testing? Can my genes tell my future? All Access DNA answers the questions you have about genetics, healthcare, and popular issues in precision medicine as it relates to our daily lives. We may even veer into territory that is no longer science fiction but science reality. Host Kate Wilson utilizes her genetic expertise and experience to interview leaders and specialists in genomic medicine and research. Join us as we empower everyone to know more about DNA in an entertaining format.","last_synced_at":"2026-09-09T04:22:04.970886+00:00","page_url":"https://stenobird.com/podcast/all-access-dna-7139504"},"episode":{"title":"Bonus-Rare Disease & Treatment Delays: Hope for Sanfilippo syndrome","slug":"bonus-rare-disease-treatment-delays-hope-for-sanfilippo-syndrome","published_at":"2026-02-28T09:00:00+00:00","page_url":"https://stenobird.com/podcast/all-access-dna-7139504/bonus-rare-disease-treatment-delays-hope-for-sanfilippo-syndrome","show_page_url":"https://stenobird.com/podcast/all-access-dna-7139504","url":"https://allaccessdna.podbean.com/e/rare_disease_sanfilippo_fda/","audio_url":"https://mcdn.podbean.com/mf/web/yi2ncs8rftndfa6z/Bonus_Ep_2_Abby8ezs6.mp3","summary":"In this heartfelt interview, Abby Milburn shares her journey as a mother of a child with Down syndrome and Sanfilippo syndrome, a rare neurodegenerative disease. She discusses diagnosis challenges, advocacy efforts, and the importance of research and policy changes to support children with rare diseases. Sanfilippo syndrome, Down syndrome, rare diseases, medical advocacy, genetic testing, FDA approval, gene therapy, medical research, advocacy, rare pediatric treatments Key Topics: Sanfilippo syndrome diagnosis and symptoms Challenges in medical advocacy and policy The role of genetic testing and family history Impact of FDA approval process on treatments Importance of awareness and community support Abby Milburn is a wife and stay at home mom to four children 5 years old and under. Her oldest daughter, Lottie, is extremely unique as she has both Down syndrome and Sanfilippo Syndrome. Lottie’s Cure Sanfilippo Foundation Page: https://give.curesanfilippofoundation.org/campaign/lottie-milburn-or-fighting-to-cure-sanfilippo/c716615 Instagram and Facebook handle: @letssavelottie Please subscribe to this podcast on Apple Podcasts, Spotify, YouTube or wherever you get your podcasts to stay updated on new episodes of All Access DNA. Listen to past episodes on your favorite podcast play by searching “All Access DNA” or by streaming from our website at allaccessdna.podbean.com Here are more resources related to today’s topic: Lottie’s Cure Sanfilippo Foundation Page: https://give.curesanfilippofoundation.org/campaign/lottie-milburn-or-fighting-to-cure-sanfilippo/c716615 Cure Sanfilippo Foundation: https://curesanfilippofoundation.org/ Senate Hearing Special Committee on Aging: From Regulator to Roadblock: How FDA Bureaucracy Stifles Innovation UX111 Gene Therapy for Sanfilippo s…","meta_description":"In this heartfelt interview, Abby Milburn shares her journey as a mother of a child with Down syndrome and Sanfilippo syndrome, a rare neurodegenerative d…","key_points":[],"chapters":[],"topics":[],"duration_seconds":2694,"processing_state":"not_requested","actions":[{"name":"request_transcript","method":"POST","url":"https://stenobird.com/v1/public/podcasts/all-access-dna-7139504/episodes/bonus-rare-disease-treatment-delays-hope-for-sanfilippo-syndrome/transcription-requests","description":"Idempotently request low-priority transcript generation for this episode."},{"name":"read_markdown","method":"GET","url":"https://stenobird.com/podcast/all-access-dna-7139504/bonus-rare-disease-treatment-delays-hope-for-sanfilippo-syndrome.md","description":"Read the agent-friendly Markdown representation of this episode resource."}]}}