Zambia Urged to Ratify African Disability Protocol as Albinism Day Commemorated
By Alain Kabinda
As Zambia joins the rest of the world in commemorating
International Albinism Awareness Day 2026, the occasion is serving as more than
a moment of recognition—it is a renewed call to confront stigma, expand
opportunities, and strengthen protection for persons living with albinism.
Across communities in Zambia and beyond, people with
albinism continue to navigate barriers that extend far beyond appearance.
Challenges linked to discrimination, limited access to healthcare, social
exclusion, misconceptions, and educational inequality remain part of daily life
for many.
International Albinism Awareness Day, observed annually on
13 June, highlights the rights, dignity, and inclusion of persons with albinism
while drawing attention to the work still needed to create equitable societies.
In schools, workplaces, and communities, persons with
albinism continue to advocate for equal access to education, employment,
healthcare, and public participation.
One of the major concerns remains access to health services,
particularly skin care and eye health support. Because albinism affects melanin
production, many people living with the condition experience increased
sensitivity to sunlight and visual challenges that require continuous attention
and protective measures.
Social attitudes continue to shape experiences for children
and adults with albinism. Misconceptions and harmful stereotypes can lead to
isolation, reduced confidence, and barriers to participation in everyday life.
For some learners, the classroom becomes a place where they
must work harder not because of ability, but because systems are not designed
with inclusion in mind.
Teachers and education advocates say practical changes—such
as improved seating arrangements, accessible learning materials, awareness
campaigns, and supportive school environments—can significantly improve
educational outcomes.
Albinism Foundation of Zambia (AFZ) Chairperson Mr. John Chiti has also called on government to urgently ratify the African Disability Protocol (ADP), saying the move is necessary to strengthen protections for persons with disabilities and address persistent discrimination against people with albinism.
(Mr. John Chiti)The call was made during commemorations of International
Albinism Awareness Day, observed annually on June 13, where disability
advocates highlighted the challenges faced by people with albinism and urged
authorities to act without further delay.
Speaking during at a media engagement, Mr. Chiti said
discrimination based on skin colour remains a major challenge for many people
with albinism.
“One challenge is discrimination which is based on skin
colour. As you know, people with albinism look different. So sometimes they are
discriminated against because of their colour. This year we are celebrating our
colour. We are celebrating our skin tone and we encourage everyone who was born
and looks different to be proud of your skin,” the spokesperson said.
He also that during this period the foundation will also use
the occasion to deliver what they described as a clear and urgent message:
Zambia must ratify the African Disability Protocol.
According to Mr. Chiti, the Protocol is Africa’s own human
rights instrument designed to address barriers affecting persons with
disabilities across the continent, including stigma, harmful practices against
people with albinism, and challenges in accessing education, healthcare,
justice, political participation and complaint mechanisms.
The Protocol complements the United Nations Convention on
the Rights of Persons with Disabilities by addressing issues unique to the
African context.
Disability rights campaigners noted that the Protocol
entered into force in 2024 after receiving the required number of ratifications
from African states. They said several countries, including Angola, Burundi,
Cameroon, the Democratic Republic of Congo, Kenya, Malawi, Mali, Mozambique,
Namibia, Niger, Nigeria, Rwanda, South Africa, Uganda and Zimbabwe, have
already ratified the instrument.
Mr. Chiti explained that signing the Protocol would indicate
support for its provisions, while ratification would create binding obligations
and pave the way for its implementation within Zambia’s legal framework.
“For over five years, OPDs have engaged, consulted and
advocated for ratification,” the Mr. Chii said.
The groups acknowledged government’s public commitment to
complete the ratification process during the first quarter of 2026, referencing
parliamentary discussions and a private member’s motion debated on July 21,
2025. However, they expressed concern that there has been no visible progress
toward depositing the ratification instrument with the African Union.
“Each month of delay prolongs the barriers experienced by
people with disabilities,” Mr. Chiti said.
He further argued that ratification would strengthen legal
protections against discrimination and harmful practices, improve
accountability, and accelerate inclusion in schools, workplaces, health
facilities, justice institutions and civic life.
Mr. Chiti further said ratification would demonstrate
Zambia’s commitment to disability rights and position the country as a regional
leader in human rights and inclusion.
He Also advocates stressed that the issue extends beyond
policy discussions and affects the daily lives of many citizens.
“Behind the policy language are real people: a child out of
school because accessibility was not planned, a qualified graduate kept out of
work, a voter turned away by a physical barrier,” the Mr Chiti said.
Mr. Chiti urged authorities responsible for social services,
justice and public administration to finalise the necessary procedures and
complete the ratification process without delay.
“This is not charity. This is justice. This is development.
This is Zambia keeping its word,” said Mr. Chiti.
International Albinism Awareness Day is commemorated
globally every year on June 13 to raise awareness about the rights, dignity and
inclusion of people with albinism.
Advocates also have argued that persons with albinism should
be viewed through the lens of capability and opportunity rather than
limitation.
Across Zambia, individuals with albinism are contributing as
professionals, entrepreneurs, students, artists, public servants, and community
leaders—challenging assumptions and demonstrating that talent and ambition are
not defined by physical appearance.
Civil society organisations and disability rights groups
continue to encourage stronger implementation of inclusive policies and broader
public education to address prejudice.
Community leaders say changing perceptions starts with
everyday interactions—recognising persons with albinism as equal citizens whose
rights and aspirations deserve protection.
This year’s commemoration is also highlighting the
importance of representation and visibility.
Young people living with albinism increasingly want more
than symbolic inclusion. They are calling for meaningful participation in
decisions that affect their education, health, employment, and future.
For families raising children with albinism, support
networks and public awareness remain essential in helping children grow with
confidence and self-belief.
International Albinism Awareness Day 2026 therefore stands
not only as a celebration of resilience, but also as a reminder that inclusion
requires action.
As communities reflect on progress made, the message
emerging from this year’s commemoration is clear: dignity, safety, opportunity,
and equal treatment should not depend on skin colour.

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