On 15 November, 14:30-15:30, our Chief Executive, Jayne Spink, and our Director of Policy, Nick Meade, hosted a webinar to update and share the key policy areas that affect the rare, genetic and undiagnosed community including our Pledge for Patients campaign. If you missed the opportunity to join us for the webinar or just want to recap what was said, you can access the slides for the webinar here, or watch a recording of the webinar below.
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