Get to Know the Palestinian Society for Bleeding Disorders (PSBD)
It is a charitable, non-profit organization officially registered with the Palestinian Ministry of Interior under number RA-22444-M, with its reference being the Palestinian Ministry of Health. The society operates in accordance with the provisions of the Charitable Associations and Non-Governmental Organizations Law No. (1) of 2000 and its amendments. The society enjoys independent legal personality and has its own financial liability, enabling it to implement its activities and programs to serve patients across the different governorates of the country.
The society is committed to standards of transparency and governance, providing annual financial and administrative reports to the official authorities in accordance with legal requirements. It also works within a humanitarian and health-focused vision aimed at improving the quality of life of people with bleeding disorders, and enhancing their access to therapeutic services as well as psychological and social support.
Basis of Work at the Society
The Palestinian Society for Bleeding Disorders bases its work on acting as a link between the Ministry of Health and patients and their families, providing a supportive environment that combines specialized medical care with psychological and social support. This is done within a framework of transparency, respect for patients’ rights, and partnership with local and international institutions.
Palestinian, non-governmental, and non-profit.
Core principle: Volunteering is the foundation of the society’s work.
Our Vision
To enhance the quality of life for patients and their families by providing comprehensive holistic care that includes medical, psychological, social, and educational services, while building an effective community awareness that supports patient empowerment, protection, and ensures their access to the services they need
Our Main Goals
Bringing patients and their families together in a family-like environment, giving them the freedom to raise their concerns.
Educating patients and their families about the disease, its treatment, causes, and ways to reduce its spread.
Documenting and activating an informational system that allows patients and their families to access medical treatment and social services from relevant authorities in a humane and civilized manner, avoiding the pitfalls of ignorance and bureaucracy.
Community education about the disease to promote positive engagement and integrate patients into public life.
Raising community awareness to reduce the prevalence of the disease in Palestinian society.
Developing programs that address the needs of patients and their families in accordance with societal norms and Palestinian laws.
Achievements and Milestones
Representation
Representing the bleeding disorders community in Palestine at various international, regional, and local seminars and conferences, highlighting its role in voicing patients’ concerns and advocating for their rights at all levels.
Advocacy
Launching local and global campaigns to raise awareness of patients’ needs in Palestine, provide necessary support, and implement international treatment protocols for patients.
Educational Materials
Producing educational materials, including a comprehensive booklet on bleeding disorders and introductory videos about the disease in Palestine.
Headquarters
The society’s headquarters is hosted at the Al-Bireh Medical Center Endowment and is used as an administrative and educational center.
Towards the Future
We focus on raising medical and psychosocial awareness in Palestine and strive to reduce new cases by emphasizing the importance of premarital screening and addressing genetic issues related to bleeding disorders.
Palestinian Hemophilia Society
Al-Bireh Medical Center, 4th Floor
Near the Family Rehabilitation Society
