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Our Activities

SASEA Strategy Objective 1: Platform strengthening

  1. Convening Partners:
    Organize virtual and in-person meetings to identify key issues and priorities for the platform and national initiatives.

  2. Resource Mobilization:
    Provide technical and financial support to facilitate activities for the platform and its partners.

  3. Representation Support:
    Assist platform members by ensuring partner representation at seminars and conferences to highlight nationally important issues and the platform’s impact.

  4. Collaborative Space:
    Create a supportive environment for platform partners to share insights, raise awareness, and collectively address critical human and health rights issues, generate evidence and data, and develop innovative models.

  5. Platform Expansion:
    Expand the platform by including new partners who share a common vision.

  6. Capacity Building:
    Enhance the capabilities of partners in collaborative research and publications.

SASEA Strategy Objective 2 : Generating data and evidence

  1. Upskilling Partners:
    Enhance research literacy among partners, focusing on community-led research and data analysis.

  2. Support Community Initiatives:
    Strengthen partners’ initiatives in community-led monitoring related to HIV, sexual and reproductive health and rights (SRHR), transgender care, viral hepatitis diagnosis, treatment, and addressing human rights violations.

  3. Documentation and Publication:
    Document and publish critical health and human rights issues affecting key populations and people with lived experiences (PWLE).

  4. Community-Led Care Models:
    Demonstrate innovative community-led care models and replicate them through South-South collaboration.

SASEA Strategy Objective 3 : Advocacy

  1. Data Dissemination:
    Share data on the effectiveness of innovative care models with all stakeholders for adaptation and scaling up.

  2. Empowerment through Rights Education:
    Equip partners with knowledge of their rights and legal protections under international covenants and national laws to advocate for the health and human rights of key populations and people with lived experiences.

  3. Utilization of Community-Led Data:
    Use data from partners’ community-led interventions as evidence to address critical health and human rights issues.