The Transplant Strong Podcast – Episode 4 features special guest Virginia Lee, sharing her transplant story and life with Wilson’s Disease.In this episode, Virginia and I talk openly about our experiences of living with Wilson’s Disease and undergoing liver transplantation. We discuss how life changes after transplant and how chronic illness impacts relationships, food choices, and everyday living.We also talk about navigating life as a transplant patient during Covid-19 and how global events can add extra challenges for people living with compromised immune systems.Topics covered include:• Wilson’s Disease diagnosis and treatment • Life before and after a liver transplant • Relationships and chronic illness • Food, diet, and lifestyle changes • Living as a transplant patient during Covid-19 This episode is ideal for:• People living with Wilson’s Disease • Liver transplant patients • Those interested in real transplant stories • Anyone seeking patient-led transplant conversations If you enjoyed this episode, please like, subscribe, and support The Transplant Strong Podcast.If you would like to join me on an episode or have any questions, feel free to reach out.🌍 The Transplant Strong Website: https://transplant-strong.com📘 Connect with me:Facebook –   / danny.hiles   Instagram –   / danny_hiles86   ✍️ Blog – Life with Wilson’s Disease:https://organtransplant.home.blog/

#TransplantPodcast #TransplantStories #WilsonsDisease #LiverTransplant #TransplantStrong

The Transplant Strong Podcast – Episode 3 features special guest Michelle El Nemnom, sharing her transplant story and experience of living with Wilson’s Disease.In this episode, Michelle and I talk about our personal experiences with Wilson’s Disease, including diagnosis, daily life, and long-term treatment.Michelle also shares the serious challenges she faces in accessing vital Wilson’s Disease medication and the ongoing struggle of getting her medication safely delivered to Beirut. Access to treatment is a critical issue for many rare disease patients, and this conversation highlights how life-threatening these barriers can be.Topics covered include:• Living with Wilson’s Disease • Diagnosis and long-term management • Access to life-saving medication • The challenges of treatment availability abroad • Patient advocacy and resilience This episode is ideal for:• People living with Wilson’s Disease • Rare disease patients and advocates • Those interested in real transplant stories • Anyone listening to a patient-led transplant podcast If you enjoyed this episode, please like, subscribe, and support The Transplant Strong Podcast.If you would like to join me on an episode or have any questions, feel free to reach out.🌍 The Transplant Strong Website: https://transplant-strong.com📘 Connect with me:Facebook –   / danny.hiles   Instagram –   / danny_hiles86   ✍️ Blog – Life with Wilson’s Disease:https://organtransplant.home.blog/

#TransplantPodcast #TransplantStories #WilsonsDisease #RareDisease #TransplantStrong

The Transplant Strong Podcast – Episode 2 features special guest Heather Lindsay, sharing her powerful transplant story and long-term experience of living with Wilson’s Disease.In this episode, Heather and I talk openly about our experiences with Wilson’s Disease, from early diagnosis through to liver transplantation. Heather shares her journey to transplant and gives a rare insight into what life looks like 29 years after a liver transplant.Long-term transplant outcomes are not talked about enough, and Heather’s story is a reassuring and inspiring example of how full and meaningful life can be decades after transplant.Topics covered include:• Living with Wilson’s Disease • Diagnosis and progression of liver disease • The liver transplant journey • Life 29 years post-transplant • Long-term health, mindset, and resilience This episode is ideal for:• People living with Wilson’s Disease • Liver transplant patients (pre and post) • Anyone looking for real transplant stories • Listeners of a patient-led transplant podcast A huge thank you to Heather for sharing her story and helping raise awareness.If you enjoyed this episode, please like, subscribe, and support The Transplant Strong Podcast.If you would like to join me on an episode or have any questions, feel free to get in touch.🌍 The Transplant Strong Website: https://transplant-strong.com📘 Connect with me:Facebook –   / danny.hiles   Instagram –   / danny_hiles86   ✍️ Blog – Life with Wilson’s Disease:https://organtransplant.home.blog/

#TransplantPodcast #TransplantStories #WilsonsDisease #LiverTransplant #TransplantStrong

In this episode I am joined by Jessica Wickers from the USA.

We discuss how Jessica's diagnoses came about and what treatment was needed to control her Wilson's Disease. 

Jessica tells us about the Zinc treatment she is currently using and there is a link here -   hhttps://www.extremev.com/zinc50mg.html 

Discount code WDAGLUZIN  

If you enjoyed or found this video interesting then please give it a thumbs up and subscribe to keep up to date with future videos.   If you would like to join me on an episode or you have any questions please fell free to find me on Facebook or Instagram. I have also added a link to my blog.   

Facebook - https://www.facebook.com/danny.hiles

Instagram - https://www.instagram.com/danny_hiles86/

Blog - https://organtransplant.home.blog/201...

Hello everyone, my name is Danny Hiles, and in this short video I share my personal journey with Wilson’s Disease — from diagnosis to how life has been since.This video is part of The Transplant Strong Podcast, a transplant podcast dedicated to sharing real transplant stories, rare disease journeys, and honest patient experiences.I talk about: • Being diagnosed with Wilson’s Disease • How it affected my life at the time • Adjusting mentally and physically after diagnosis • The positives and opportunities that can come after a rare disease diagnosisMy hope is that this video helps shed some light on what life with Wilson’s Disease can look like, especially for those who are newly diagnosed or supporting someone living with a rare liver disease.While Wilson’s Disease can be overwhelming at first, there is life, strength, and positivity after diagnosis, and I want this video to reflect that.If you’d like to know more about my story, I’ve been writing a blog over the last few months that goes into more detail and answers many of the questions people often ask.✍️ Blog – Life with Wilson’s Disease & Transplant Stories👉 https://organtransplant.home.blog/201...🌍 The Transplant Strong Website https://transplant-strong.com📘 Find me on social media:Facebook –   / danny.hiles  Instagram –   / danny_hiles86  If this video helps you, please consider liking, sharing, or subscribing — it really helps get these transplant stories out to the people who need them most.#TransplantPodcast #TransplantStories #WilsonsDisease #RareDisease #LiverDisease #TransplantStrong

Welcome to Danny Chats,  this episode is a little introduction to the podcast and what it is about. 

Thank you for listening I hope you find it informative and useful, if you do please remember to like, subscribe and comment on the video.