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Ethan and Me with Geraldine Renton

An episode of the Rare Genomics / RareShare Podcast Series: Ask the Expert & Patient Navigation podcast, hosted by Rareshare, titled "Ethan and Me with Geraldine Renton" was published on May 26, 2021 and runs 45 minutes.

May 26, 2021 ·45m · Rare Genomics / RareShare Podcast Series: Ask the Expert & Patient Navigation

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Listen to RareShare's latest podcast with Geraldine Renton, book author and Irish mother of a Hunter Syndrome child. In this episode, Geraldine tells of her family's journey navigating the challenges of a rare disease that led to the writing of her book Ethan and Me. Hear about their courageous battle with adversity, as they learned of the genetic enzyme deficiency behind the disease and faced its unrelenting consequences, leading to Ethan's passing in late 2020. From learning about Ethan's diagnosis, to locating support and treatments, to just being a mom, the podcast paints a broad perspective about confronting a rare disease. This very candid and detailed account, which includes many lighter enduring moments about life with Ethan, is heartwarming, informative and inspirational.  

 

From the book Ethan and Me:  "You're now in a secret world. You'll see things you never imagined... yet you'll also witness so many everyday miracles. You'll treasure things most wouldn't think twice about. You'll become an advocate, an educator, a specialist and a therapist, but most of all you'll be Mom or Dad to the most wonderful child."

rare stories Podcast - gemeinsam weniger selten CHIESI & Patients In Rare Stories erzählen Menschen von ihren Erfahrungen mit seltenen Erkrankungen. Sie teilen ihre persönlichen Geschichten, geben wertvolle Alltagstipps und schenken Mut. Auch Angehörige berichten von ihren Erlebnissen, und Expert*innen liefern hilfreiche Einblicke. Jeden Monat eine neue Folge mit inspirierenden Geschichten und spannenden Insights. Hör mal rein und lass dich berühren! Digitally Rare Jonathan Mann Matt Condon and Jonathan Mann explore what it means to own things on the blockchain and beyond. Living Ultra Rare: The ABL+ Podcast ABL+ Foundation Barry Funkhouser, Paul Biderman and guests discuss living with ultra rare diseases. The goal of this podcast is to raise awareness about rare illnesses and the people who live with them.Abetalipoproteinemia and Related Disorders Foundation is a non-profit, volunteer organization that provides guidance on needed scientific research, diagnosis, and management of abetalipoproteinemia and related hypolipidemias, such as chylomicron retention disease and familial hypobetalipoproteinemia. To donate: https://www.ablfoundation.org/donate The Very Rare Show Jessica, Janet My name is Janet, and I want to invite you into my world. Join me on a journey where my Co-host Jessica and I interview guest who have unravelled and realize their purpose of existence, who are on their path to destiny. Moreover, allow me to take you on a ride, where I go beyond Western Medicine into the Universal science of a rare illness that helped me transform into the co-creator of my life. This show is for you, who is willing to change perspective in order to fulfill your life purpose. I welcome you to The Very Rare Show.
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