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S5 E2 - DHDDS: Turning a Diagnosis into a Global Support Network

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Manage episode 487682927 series 3555329
Content provided by NHS Genomic Medicine Service. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by NHS Genomic Medicine Service or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://ppacc.player.fm/legal.

In this episode, Helen is in Guy's Hospital London, supported by the South East Genomic Medicine Service, talking to Mel Dixon about her experience with the rare genetic condition DHDDS.

After two of Mel's children were diagnosed with DHDDS, Mel and her husband Charlie founded Cure DHDDS, a charity set up to raise awareness, support families and help drive research into the ultra-rare DHDDS gene mutations. Mel tells us about their experience as parents dealing with the journey through the diagnostic pathway, and setting up a global support network for other families affected by this condition.

  continue reading

26 episodes

Artwork
iconShare
 
Manage episode 487682927 series 3555329
Content provided by NHS Genomic Medicine Service. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by NHS Genomic Medicine Service or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://ppacc.player.fm/legal.

In this episode, Helen is in Guy's Hospital London, supported by the South East Genomic Medicine Service, talking to Mel Dixon about her experience with the rare genetic condition DHDDS.

After two of Mel's children were diagnosed with DHDDS, Mel and her husband Charlie founded Cure DHDDS, a charity set up to raise awareness, support families and help drive research into the ultra-rare DHDDS gene mutations. Mel tells us about their experience as parents dealing with the journey through the diagnostic pathway, and setting up a global support network for other families affected by this condition.

  continue reading

26 episodes

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