The Rare Disease Podcast
3.5 million people in the UK live with a rare disease, so while each disease is individually rare, together rare diseases are common. Hear interviews with patients, clinicians, advocates, students and researchers focusing on rare disease in clinical medicine.
This podcast is brought to you by Medics for Rare Disease. Podcast distributors create their own transcripts and M4RD doesn’t take responsibility for them
The Rare Disease Podcast
Genomics in Primary Care: Why Your Role Matters More Than Ever!
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For this week's episode of the podcast Lucy chats to Isobel, Philandra and Vicki who are from the GMSA (Genomics Medicine Service Alliance). They are putting on a fantastic online event alongside the University Hospital Birmingham all about genomics in primary care and would love as many of you to sign up as possible!
Lucy our host of the podcast will also be speaking at the event which takes place on the 12th of June, online.
You can sign up to the GMSA event here https://www.tickettailor.com/events/nhscentralandsouthgenomics/1676787
You can sign up to the recommendations workshop Lucy mentions at the start here: https://www.m4rd.org/event/recommendation-writing-workshop/
You can visit Central and South Genomics’ website here: https://centralsouthgenomics.nhs.uk/
Sign up to their mailing list here: https://mailchi.mp/a683c3c0bfe6/nhs-central-and-south-genomics-mailing-list
To view all their platforms, including their events, click here: https://linktr.ee/centralsouthgenomics
Views, ideas and opinions expressed in this podcast are personal to the individual and Medics4RareDiseases does not accept responsibility for those expressed by guests.
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M4RD does not endorse any companies or products that it receives sponsorship from. For more information please see the show notes and www.m4rd.org/sponsors #DareToThinkRare