International Albinism Conference
Albinism is a relative rare genetic condition that affects people around the globe. Due to a lack of pigmentation, people with albinism are vulnerable to skin cancer and are visually impaired. Albinism is not well understood, which results in misconceptions, erroneous beliefs and various forms of harm.
The conference will advance understandings of albinism, bringing together experts on human rights, advocacy, social inclusion, climate change, policy making, genetics, ophthalmology, and dermatology.
Participants will include albinism advocates and associations, UK and international NGOs and charities, scientists and researchers, medical and education professionals, and policymakers.
Target Audience
Albinism affects people internationally and impacts families and communities. This event brings together albinism advocates and associations, UK and international NGOs and charities, scientists and researchers, medical and education professionals, and policymakers to identify new priorities for advocacy and research.
Key Dates and Timings
The conference will be held on 16-17 September 2025 at Lancaster University.
Sponsorship is requested as a one-off for this event. Please contact the Organiser by 20th June regarding sponsorship.
Specific Opportunity Details
The conference is not-for-profit and sponsorship will directly support the participation of delegates from the global south and albinism advocates.
The conference will be publicised on our conference webpages and on social media by Lancaster University and its partners, which have significant reach.
Features and Benefits
Sponsors will be recognised in the conference proceedings, on our website and social media, and acknowledged in the opening remarks and all conference outputs.
Other Partners
United Nations Independent Expert on the Rights of Persons with Albinism; Open Eyes Foundation
Investment
A one-off sponsorship of any amount over £100 is welcome in support of this important event.