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Albinism Advocates Issue Two-Week Deadline: Demand Health Minister Act on Urgent Medical Supply Gaps

by Alphanso G. Kalama
June 15, 2026
in News
Reading Time: 3 mins read
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Published: June 15, 2026

Monrovia – The Liberia Albinism Society (LAS) has given Health Minister Dr. Louis M. Kpoto a firm two-week deadline to respond to their demands for essential medical supplies.

LAS Executive Director Madam Patricia N. Logan made the announcement over the weekend in Monrovia during activities marking International Albinism Day. The event was held under the theme “Proud in My Skin, One” and received support from Apex Optics Eye Clinic, which provided free eye screenings, eyeglasses, food, and other aid to LAS members.

Speaking at the ceremony, Madam Logan voiced strong disappointment over what she called the government’s failure to meet the health needs of persons with albinism. “We are giving the Minister of Health two weeks to respond to our request for medical supplies and support. If there is no satisfactory response, we will take steps to ensure no one works at the Ministry of Health,” Logan warned.

The deadline comes as concerns grow over the health conditions facing the albinism community, which requires specialized medical attention due to unique complications.

Director Logan also stressed the significance of a 31-bedroom clinic that was repurposed into a hospital for the albinism community. “You cannot set up a facility meant for us and then deny it the needed medical supplies,” she stated.

In addition, Madam Logan cautioned that if the Ministry of Health fails to act, the group will intensify its campaign by marching to the Executive Mansion to demand intervention. “We will not keep quiet while our people continue to lack basic medical resources,” she insisted.

LAS continues to push for the rights and health of Liberians with albinism, drawing attention to the visual and skin-related challenges tied to the condition.

Webster G. Tarlee Yeanay, General Manager of Apex Optics Eye Clinic, gave an overview of the program, noting that individuals with albinism often experience reduced visual acuity, nystagmus, and light sensitivity. “There is no cure for albinism, but we can raise their quality of life by offering proper optical correction and low-vision care,” Yeanay said.

LAS says its call to action targets both immediate supply shortages and wider awareness of health issues affecting people with albinism.

Yeanay added that refractive errors, extreme light sensitivity, and the need for specialized treatment are common among persons with albinism, making access to proper medical resources vital. He called on the public to support the community and push for their right to health and well-being.

The organization says it hopes the two-week ultimatum will force a quick and concrete response from health officials so no member of the albinism community is denied the care they need.

Tags: Albinismdisability rightshealthcareHuman RightsLiberia Albinism SocietyLouis KpotoMinistry of Health
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Alphanso G. Kalama

Alphanso G. Kalama

Alphanso G. Kalama is a Liberian journalist with over seven years of experience in broadcasting and newsroom reporting, specializing in environmental issues and human-interest stories. He began his career in 2018 as a rural reporter in Lofa County with Radio Life and has since contributed to leading radio, print, and online outlets in Liberia.

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