Going Virtual with Patient and Caregiver Support Meetings

To reach the RDSA vision of readily accessible care and support for those affected or at risk of rare and congenital disorders, we believe we not only need to unite with support groups but to work together as a team.

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In this three-part webinar series, we have partnered with Novartis to assist our nascent and budding support groups, grow into fully fledged, independent organizations.

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Join us on Wednesday 30 June at 4pm, as Kelly du Plessis talks about what a valuable tool a webinar can be to connect and engage with the patients and families that fall within your care.