Libyan Association for Muscular Dystrophy Patients Urges Government to Address Disability Rights

The Libyan Association for Muscular Dystrophy Patients has announced plans to organize a peaceful protest to demand rights for people with disabilities, retirees, widows, and divorced women. They cite continued delays in benefits and deteriorating living conditions. The association, in a Facebook post on November 13, stated that the upcoming protest aims to push for the disbursement of delayed home care benefits since 2018.

The association is seeking to improve the value of basic pensions, currently at 650 Libyan dinars, and provide high-quality medical equipment and mobility aids. They also want to complete the distribution of cars owed to people with disabilities. The group blames the government and relevant institutions, including the General Authority for the Social Solidarity Fund, for the ongoing struggles faced by these groups.

The Libyan Association for Muscular Dystrophy Patients has previously called on people with disabilities, widows, and divorced women to prepare for protests to demand their rights. They emphasize that their movement will be peaceful and reject being labeled as chaotic. The association has criticized the government's lack of response to repeated demands.

The association highlighted the plight of children suffering from spinal muscular atrophy, including one child recently hospitalized due to health complications. The child is in need of the genetic injection "Zolgensma". The association stressed that the upcoming protest is also aimed at demanding healthcare and living rights for people with disabilities.

Continued delays in benefits and provision of medical needs exacerbate the suffering of patients and their families, according to the association. They urge relevant authorities to assume responsibility and respond to the demands of those entitled to rights. The association holds the government and institutions accountable for the ongoing situation.

The planned protest seeks to draw attention to the struggles faced by vulnerable groups in Libya. The association's efforts aim to secure improved living conditions and healthcare for people with disabilities. They emphasize the importance of government support and responsiveness to the needs of these groups.

The Libyan Association for Muscular Dystrophy Patients continues to push for change, emphasizing the need for collective action to address the challenges faced by people with disabilities. Their efforts highlight the importance of collaboration between government institutions and civil society organizations to ensure the rights of all citizens are protected and respected.

Key points

• The Libyan Association for Muscular Dystrophy Patients demands improved living conditions and healthcare for people with disabilities.