Podcast thumbnail for C18 Europe

by Richard Davison

6 episodes
Updated Daily
Accepts GuestsHas SponsorsLocation πŸ‡¬πŸ‡§

Podcast Overview

This is a podcast hosted by the Chromosome 18 Registry and Research Society (Europe) who are a charity representing the families of those affected by a Chromosome abnormality. In this podcast we aim to fairly informally invite guests to talk about their experiences so that these experiences can help those affected by C18 issues. We aim to cover topics like life stories, medical problems and treatments, life transitions and sibling issues.

Language

πŸ‡ΊπŸ‡²

Publishing Since

11/19/2020

1 verified contact email on file for C18 Europe

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Recent Episodes

Episode thumbnail for Interview with Eve Rushmer

March 18, 2021

Interview with Eve Rushmer

<p>Eve is our first self-advocate on the podcast and in the interview we chat about her life and work. &nbsp;This is a remarkable story of resilience and determination to succeed at school, learn to drive and get a good job. On top of that Eve has completed a number of daring and demanding activities to raise money for Chromosome 18 Europe which of course were extremely grateful. I am sure that you will enjoy our chat.</p>

Episode thumbnail for Parent Story from one of our founding members Bonnie McKerracher

February 17, 2021

Parent Story from one of our founding members Bonnie McKerracher

<p>Bonnie is one of the founding members of Chromosome 18 Registry and Research Society (Europe) and in this episode she tell us of her story about her daughter Kathryn who is affected by 18q-. As Kathryn is now over 40 much of Bonnie's story is one of discovery about Kathryn's condition and finding the best medical and schooling options for her at a time when very little information existed about chromosome 18 abnormalities. In addition to telling us her story as a parent Bonnie gives us a brief history of the establishment of the Society the why and how it happened.&nbsp;</p>

Episode thumbnail for Parent Stories: Sara Jackson

January 17, 2021

Parent Stories: Sara Jackson

<p>This is the first in our Parent Stories, series where I interview Sara Jackson who is one of the management committee members. Sara has been involved with C18 Europe for a very long time contributing in virtually every way since the charity started. In this interview Sara talks about her journey with her son Louis and I am sure that many of you will recognise parts of her journey as you too have been there. I also hope that this story provides help and &nbsp;support to everyone.&nbsp;</p>

6 total episodes available

Deep-dive analytics for C18 Europe

Frequently asked questions

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What is C18 Europe?

This is a podcast hosted by the Chromosome 18 Registry and Research Society (Europe) who are a charity representing the families of those affected by a Chromosome abnormality. In this podcast we aim to fairly informally invite guests to talk about their experiences so that these experiences can help those affected by C18 issues. We aim to cover topics like life stories, medical problems and treatments, life transitions and sibling issues.

How often does this podcast release new episodes?

This podcast updates daily.

Where can I listen to this podcast?

This podcast is available on 4 platforms including Apple Podcasts, Spotify, and more. You can also use the RSS feed directly.

Does this podcast accept guests?

Yes, this podcast regularly features guests.

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