Season 2 - Ep 1 Scotland's Poland Syndrome Advocate: Jen's Inspiring Journey

Send us Fan MailWelcome to What about PS? Podcast the show where we delve into remarkable stories and journeys that inspire us all. I'm your host, Giselle, and today we have a very special episode in honor of Rare Disease Day.Join us as we shine a light on Jen's extraordinary journey to diagnosis in Scotland for her son and her unwavering commitment to educating health care professionals in Scotland about Poland Syndrome. Jen's story is not just about resilience; it's about turning challenges into opportunities for advocacy and education about Poland Syndrome in Scotland.In this episode, we'll hear from Jen herself as she shares her experiences, challenges, and triumphs. We'll also explore the importance of raising awareness about rare diseases and the impact it has on individuals and communities.So, whether you're familiar with our podcast or just tuning in for the first time, get ready for a deeply moving and insightful conversation that will leave you feeling inspired.Sit back, relax, and join us as we celebrate Rare Disease Day with Jen's incredible story. You won't want to miss this empowering episode! #RareDiseaseDay #PodcastEpisode 🌍 Support Our Global Mission PIP-UK is a charity without borders, providing 1:1 advocacy and specialist clinics for the Poland Syndrome community worldwide. Help us keep these lifelines free: Donate Here: https://bit.ly/4df3fyr📋 Be Counted Join the Global Poland Syndrome Community Register to help us build a future of better care: https://bit.ly/4cCpC1t✨ Connect & Support If this episode helped you, please Rate & Review the show on Apple Podcasts or Spotify—it helps other families find us!Find us online: 🌐 Website: https://pip-uk.org/ 📱 Instagram & TikTok: @polandsyndromepipuk 👥 Facebook: pip.uk.org 💼 LinkedIn: PIP-UK🎙️ Want to share your story? Email us at [email protected]