Videos for the Society for Mucopolysaccharide Diseases to communicate rare diseases

January 2021 

We’re delighted to be working with the marketing and communication team at the MPS Society to help them to communicate rare genetic diseases to people with these conditions and their families.

The society aims to transform lives through support, research and awareness building, but also by helping people to live life to their full potential, helping them to recognise that they are not alone, and by providing care today and hope for the future.

We will be developing a series of short, informative and visual animations that help people feel informed about their newly diagnosed condition, less anxious and more willing to connect with the society and their wider community of care.

We will be running workshops with patients, families and healthcare specialists to understand what matters to them and have started to develop initial scripts that will help stakeholders join in with the creative process.

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