Patient groups play an invaluable role in the rare disease field by supporting patients and families, collecting data and pushing for policy, research and treatments. However, groups are only as strong as their community. To deliver these vital services rare disease stakeholders need to know the group exists.
This is why increasing the visibility of your patient organisation is so important. Being visible means groups can provide newly diagnosed patients, many of whom have gone through a long and isolating journey, with crucial support. Being connected with more patients also allows groups to collect more data which is key in understanding their specific disorder. As well as patients, it is important for groups to be visible to healthcare professionals who will diagnose the disorder and could refer new patients to the group.
For many patient groups working with limited resources, knowing how to improve awareness of your organisation may not be obvious. We have designed this webinar to give patient group leaders practical tools and tricks they can use to increase their visibility both in the online and in-person setting.