Many 2SLGBTQIA+ people living with dementia hesitate to access care out of fear of discrimination. This can lead to later diagnoses, fewer supports, and greater isolation. Together can help build a inclusive dementia care systems. Learn how: http://alzheimer.ca/manyfaces #Pride
— Alzheimer Society of Canada (@AlzCanada) June 11, 2025
Yesterday we joined the world in marking #IAAD2025 under the theme: "Demanding our Rights: Protect our Skin, Preserve our Lives." #albinismawareness
Today, on International Albinism Awareness Day, I stand in solidarity with all persons with albinism across Nigeria and the world. This year’s theme, “Demanding our Rights: Protect our Skin, Preserve our Lives,” is a great call to action. It reminds us that people with albinism Show more Woye and 2 others
— Remi Tinubu Support Organization RETSO (@RemiRETSO) June 13, 2025
Today, on International Albinism Awareness Day, I stand in solidarity with all persons with albinism across Nigeria and the world. This year’s theme, “Demanding our Rights: Protect our Skin, Preserve our Lives,” is a great call to action. It reminds us that people with albinism Show more
— Sen Oluremi Tinubu, CON (@SenRemiTinubu) June 13, 2025
Persons with albinism face daily threats to their health, safety & dignity. On #IAAD2025, UN Malawi stands in solidarity to demand protection, inclusion & equal rights for all. Demanding Our Rights: Protect Our Skin, Preserve Our Lives Read more: https://malawi.un.org/en/296203-united-nations-malawi-statement-international-albinism-awareness-day-2025… UNDP Malawi and 9 others
This is a reflection of how deeply inhumane we are with difference as a society. How quick we are to exclude people because of a condition they were born with. People with disabilities…with albinism…we are so so discriminatory Quote CHUKS @ChuksEricE · Jun 10 0:14 Man laments after reportedly being denied entry into Emirate Mall in Ilorin, Kwara State, due to the condition of his baby
— Super-Megazillionaire Misty (@MistuRants) June 11, 2025
One minute, you’re married. The next, all four of your kids are born with albinism in a society that doesn’t see them as children but as “deities,” “omens,” “ritual objects.” Watch the full #InternationalAlbinismAwarenessDay documentary now on YouTube: https://youtu.be/RIZnV8_Z_rw
— Miss Albinism Advocacy Pageant Is Coming 👸🏼 (@mistyglamcorp) June 13, 2025
Happy International Albinism Awareness Day to me! I’m grateful for the life I have as a person – yes, a person with albinism – but first of all, A PERSON. A full human being. Not a condition. Not an exotic species. Not a stereotype. Just a girl with…
— Black Girl No Melanin (@ItsEnnieBee) June 13, 2025
On this World Albinism Awareness Day, we're proud to share the official trailer for We Hid In The Sun - a story that speaks to truth, survival, and the urgent need for representation.
Today, we mark a decade of global recognition and advocacy for the rights of persons with albinism. This year’s theme — “Demanding our rights: Protecting our skin, Preserving our lives” — is a reminder of the continued fight for dignity, inclusion, and justice
International Albinism Awareness Day is a global observance that seeks to raise awareness about albinism and the challenges faced by people with the condition. Across the world, this day aims to shed light on the social, cultural, and medical aspects of albinism, as well as advocating for the rights and well-being of those affected. The observance encourages solidarity and empathy, with the ultimate goal of fostering an inclusive and understanding environment for people with albinism.
The United Nations General Assembly adopted a resolution in 2014 to designate June 13th as International Albinism Awareness Day, in response to the ongoing discrimination, stigmatization and violence faced by those with the condition. As a diverse and inclusive society, Canadians are encouraged to participate in the observance to support people with albinism, promote a greater understanding of the challenges they face, and learn about the various aspects of albinism that extend beyond its physical manifestations.
In Canada, various organizations, community groups, and individuals commemorate International Albinism Awareness Day by hosting events, workshops, and discussions that highlight albinism and the experiences of those living with the condition. This may include educational initiatives that seek to dispel myths and misconceptions, fundraisers to support research and advocacy efforts, or artistic and cultural celebrations that showcase the talents and resilience of the albinism community. By engaging with these customs and activities, Canadians emphasize their commitment to fostering an inclusive society that values the contributions and perspectives of all its members. International Albinism Awareness Day is observed on the 13th of June each year.
Top 8 Facts for 2026 International Albinism Awareness Day in Canada
International Albinism Awareness Day, observed annually on June 13, was established by the United Nations largely due to the advocacy of the Canadian non-governmental organization Under the Same Sun, which worked alongside international diplomats to pass the historic 2014 resolution.
A significant portion of online interest in Canada is driven by the work of Peter Ash, a prominent Canadian philanthropist and founder of Under the Same Sun who has been a global leader in protecting the human rights of people with albinism.
The award-winning memoir Beyond the Pale: Folklore, Family, and the Mystery of Our Hidden Genes by Canadian author Emily Urquhart provides an intimate look at raising a child with albinism in Canada and has been recognized as a Globe and Mail Best Book.
The 2025 global theme, Demanding our rights: Protect our skin, Preserve our lives, continues to resonate into the 2026 observance by highlighting the life-saving necessity of viewing sunscreen as an essential medicine rather than a cosmetic product.
Canadian filmmaker Kim Nguyen brought international attention to the experiences of people with albinism through his critically acclaimed 2012 film War Witch, also known by its French title Rebelle, which features a young boy with the condition.
Statistical data indicates that approximately 1 in 20,000 Canadians are born with albinism, a rate that suggests about 18 babies are born with the rare genetic condition in Canada every year.
Social media personality Oceanne Comtois, a legally blind lifestyle influencer from Ottawa, has gained a massive following by sharing her daily life and educating millions on the realities of living with albinism in Northern Ontario.
The ongoing research project Albinism Birthing Stories in Canada is one of the first studies to specifically investigate the psychosocial experiences of Canadian mothers and the healthcare journeys of families impacted by the condition.
In the News and Trending in Canada for International Albinism Awareness Day
Register for the virtual choir hosted by National Organization for Albinism and Hypopigmentation.
Explore a reading list that can help educate and spark conversation about albinism.
Learn about albinism and share your knowledge with others to promote understanding and acceptance. You can visit websites like Albinism Fellowship of Canada (www.albinismcanada.com), National Organization for Albinism and Hypopigmentation (www.albinism.org), or watch documentaries like Born This Way: The Inner Journey of Albinism to gain more insight.
Donate to organizations that work on improving the lives of people with albinism. Some prominent organizations in Canada include the Albinism Fellowship of Canada and the Canadian Albinism Network.