Registration is open for our 3rd Annual Rare Disease Patient Network Meeting in Wales. The event is taking place on 18 October at the Park Inn, Cardiff City Centre and will bring together patients, families, health professionals and researchers with an interest in rare diseases.
Speakers for this year's event include:
We will also be hearing from two patient perspectives talking about their experiences of living with an ultra-rare condition and living with an undiagnosed genetic condition.
Members of the Genetic Alliance UK team will be launching our Welsh Patient Charter on access to orphan and ultra-orphan medicines and talking about our latest research project on mental health.
We look forward to seeing you for a great day of excellent talks and networking opportunities!
For more information, please contact the Policy & Engagement Manager in Wales, Emma Hughes.
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