Pakistan still does not maintain a national registry of people with albinism — a genetic condition in which the body produces little or no melanin. This makes skin and eyes particularly vulnerable to solar radiation and increases the risk of skin cancer and vision problems. Activists and human rights defenders point out that the absence of reliable data on the number of such people deprives them of targeted government support. Without official statistics, it is difficult to develop assistance programs in schools, the healthcare system, and the labor market. People with albinism often face discrimination, lack of access to sunscreen, and specialized medical care. Experts emphasize that the situation is worsened by climate change: rising temperatures and increased solar activity raise health risks for this population group. In particular, more intense ultraviolet radiation increases the likelihood of burns and skin cancer in people with albinism. Activists are calling on Pakistan's authorities to conduct a census of such citizens in order to obtain accurate data on their numbers and needs. They insist on the need to develop special programs in education, including adapting the learning process for children with vision impairments, as well as expanding access to medical services, including regular skin examinations and provision of sunscreen. Additionally, human rights defenders are advocating for measures to combat stigmatization and create conditions for employment of people with albinism. So far, no concrete steps have been taken by the government, and the fate of the initiative remains unclear.