Hepatitis Foundation of Ghana

Email

info@hepatitisghana.org

Phone

M: +233-20-826-9214

Web

www.hepatitisghana.org

Address

PO Box GP 21325, Accra 21325 Ghana
About Hepatitis Foundation of Ghana

Hepatitis Foundation of Ghana is a patient’s organization and non-profit, non-governmental organization (NGO) registered in Ghana. It seeks to promote awareness of the prevalence and incidence of viral hepatitis in Ghana, and to educate the public in the prevention of the spread of the virus and the available treatment options. We also provide care and psychosocial support to the infected and affected people and their families. In addition, it seeks to serve as the primary source of information for patients and their families.

VISION

Our vision is to eliminate new viral hepatitis infections and improve the quality of life for individuals living with chronic hepatitis B and C.

MISSION

The mission of the Hepatitis Foundation of Ghana is establishing a uniform and fair approach to the effective prevention and comprehensive management of Hepatitis B among people and their families in Ghana.

OUR CORE VALUES

Competence with responsibility and professionalism are our core values. With integrity and being transparent in everything we do, we accept responsibility for our collective and individual actions. Our focus is to work effectively to serve individuals living with viral hepatitis and the larger community in Ghana. Having respect for all, we affirm the dignity and contribution of community participants, development partners, donors and staff as we work for the better of people living with viral hepatitis in Ghana.

OBJECTIVES

  • To prevent Hepatitis B spread amongst people or patients and their families.
  • To provide treatment, care support and psychosocial support for infected and affected people and their families.
  • To provide protection from stigma and discrimination in the houses, churches, market places and offices living with or affected by Hepatitis B.
  • Promoting disease awareness, supporting immunization and treatment initiatives, and serving as the primary source of information for patients and their families and the general public.
  • To empower young people, to promote their rights and to inform them about how Hepatitis cannot be transmitted, and how they can protect themselves.
  • To draw the attention of people in general and those in positions of authority in particular to accept the reality of Hepatitis in our communities, and to recognize the rights of people living with Hepatitis.
  • To reject myths and misconceptions, and fight unnecessary Hepatitis discrimination