Albino Society Issues Ultimatum To MoH

By Domingo Dargbeh

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The Liberia Albino Society (LAS) has issued a stern ultimatum to the Minister of Health, Dr. Louis M. Kpoto.

 Members of the Society have demanded an urgent action regarding the lack of medical supplies provided to the organization.

LAS Executive Director, Patricia N. Logan, made the pronouncement over the weekend in Monrovia during the commemoration of International Albino Day.

The Day was celebrated under the theme: “Proud in My Skin, One.”

Apex Optics Eye Clinic which offered ‘free eye tests, eyeglasses, food items, and other resources’ to LAS members supported the event.

Madam Logan expressed deep frustration over “government’s neglect of the needs of albino individuals.

“We have given the Minister of Health two weeks to respond to our demands for medical supplies and support. If we do not receive a satisfactory response, we will take action to ensure that no one goes to work at the ministry.”

The ultimatum comes amid growing concerns regarding the health and well-being of the albino community, which often faces unique medical challenges requiring specialized care.

Madam Logan highlighted the importance of a 31-bedroom clinic that has been transformed into a hospital for the albino community.

She said: “You cannot have a facility dedicated to our needs, and refused to provide the necessary medical supplies.”

Madam Logan warned that if the ministry does not address their concerns, they will escalate their efforts by marching to the Executive Mansion to demand action.

“We will not remain silent while our community suffers from a lack of essential medical resources.”

Albinos have actively advocated for the rights and health of individuals with in Liberia. They have often highlighted the various ocular and visual challenges associated with their condition.

Apex Optics Eye Clinic General Manager, Webster G. Tarlee Yeanay, who provided an overview of the program, noted that individuals Albino often experience visual challenges, including reduced visual acuity, nystagmus, and light sensitivity.

“While we cannot cure albinism, we can improve the quality of life for those affected by providing appropriate optical corrections and low-vision support.”

LAS call to action seeks to address immediate medical supply needs while raising awareness about the health issues faced by the albinos.

Yeanay said, refractive errors, photosensitivity, and the need for specialized care are prevalent among individuals with albinism, making access to adequate medical resources crucial.

He urged the public to stand in solidarity with individuals living with albinism and to advocate for their rights to health and well-being.

The organization expressed the hope that their ultimatum will prompt a swift and meaningful response from health authorities to ensure that no one in the albinos’ community is left without the medical care they deserved.

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