Podcast Series

It's a Rare Thing

It’s a Rare Thing is a podcast series produced by the Ann Conroy Trust to highlight the experiences of people living with syringomyelia and Chiari malformation. You can listen on YouTube and Spotify via the links or QR code below.
QR code linking to the "It's a Rare Thing" podcast series by Ann Conroy Trust.

The series includes some personal stories and experiences from people who are living with Chiari malformation and/or syringomyelia, there’s also a podcast taking a look at what support The Ann Conroy Trust provides.

The series supports the Charity’s aim to raise awareness and understanding of Chiari malformation and syringomyelia, and to help people to ‘live with’ rather than ‘suffer from’ these conditions.

The series aims to be positive and educational, and we hope it will inspire listeners to live their lives to the fullest, despite being diagnosed with a rare neurological condition.

The aim of the podcasts is to help others, especially those who have recently been diagnosed with the condition/s, by trying to ease any fears they may have and to offer them some optimism and let them know that they are not alone and that there is a wider community and support out there for them.

We hope that by listening to the podcast series, it will offer some support and reassurance to anyone who is going through a similar experience.  It’s so beneficial hearing others talk about how they live with their condition/s. Hearing it from a personal perspective can be really helpful.

Everyone at the Ann Conroy Trust would like to thank the volunteers and contributors who have given their time to create this series.

Get Involved!

Would You Like to Feature in a Future Podcast?

We are looking for more people to feature in the podcast series.  Do you currently live with Chiari malformation and/or syringomyelia.  Do you have a positive mindset and an optimistic outlook, are you resilient to life’s challenges. Would you like to share your story and experiences with us and also provide some hope and reassurance to others who may have recently been diagnosed with the condition/s.  If so, get in touch with us via info@annconroytrust.org and provide us with your contact details.