Building a Stronger Rare Disease Community Together

We believe breakthroughs happen when patients, families, healthcare professionals, researchers, and advocates unite.

Our Role in the Rare Disease Community

At Dawn Therapeutics, our work extends far beyond the laboratory. We aim to empower, connect, and inspire the communities we serve by:

  • Partnering with patient advocacy organisations
  • Supporting awareness campaigns for rare and complex diseases.
  • Creating educational content accessible to all audiences.
  • Facilitating community-driven research initiatives.

Partnerships That Make an Impact

We collaborate with:

Non-Profit Organisations

To fund awareness events, educational materials, and support programmes.

Advocacy Groups

To ensure patient perspectives shape our research priorities.

Educational Institutions

To bring genetic science into schools and universities.

Global Alliances

For rare disease policy advocacy at national and international levels.

Events & Initiatives

Rare Disease Day Campaigns – Highlighting patient stories on a global stage.

Awareness Walks & Fundraisers – Supporting research and patient services.

Virtual Community Town Halls – Sharing progress and gathering feedback directly from families and advocates.

Educational Webinars – Featuring leading experts in genetics, neurology, and patient care.

Empowering Patient Voices

We provide platforms for patients and caregivers to:

  • Share personal stories that inspire change.
  • Join advisory boards to guide clinical trial design.

Contribute to natural history studies and registries

Community Resources

  • Educational Hub: Clear, accessible explanations of targeted diseases.
  • Advocacy Toolkit: Resources for hosting your own awareness events.
  • Funding Support: Microgrants for community-led initiatives.

ESG & Social Responsibility

Our community engagement is part of our broader Environmental, Social, and Governance (ESG) commitments:

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