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One Family's Rare Disease Odyssey - CRELD1, Pt1
Manage episode 443937755 series 3555329
Innehåll tillhandahållet av NHS Genomic Medicine Service. Allt poddinnehåll inklusive avsnitt, grafik och podcastbeskrivningar laddas upp och tillhandahålls direkt av NHS Genomic Medicine Service eller deras podcastplattformspartner. Om du tror att någon använder ditt upphovsrättsskyddade verk utan din tillåtelse kan du följa processen som beskrivs här https://sv.player.fm/legal.
This week we come to you from the heart of Guys Hospital, London, supported by the South East Genomic Medicine Service Alliance.
In the first part of this 2-part episode, Helen talks to Adam Clatworthy about his family's diagnostic odyssey that eventually saw 2 of his children diagnosed with the rare disease, CRELD1. Sharing the reality of their journey and daily experiences, we get an insight into the search for a diagnosis.
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