Soa Aids Nederland (SANL), host organisation of the network AIDS Action Europe (AAE), enhances scale and quality of the Dutch contribution to the (inter)national response to HIV/AIDS/STIs.
AAE’s mission: to unite civil society to work towards a more effective response to the HIV epidemic in Europe, striving for better protection of human rights and universal access to prevention, treatment, care and support. Aiming for a reduction of health inequalities focussing on key vulnerable populations and Eastern Europe/Central Asia.
AAE uses its status as regional network of ICASO (International Council of AIDS Service Organizations) to further its mission. We vision a world where people living with and affected by HIV/AIDS can enjoy life free from stigma, discrimination, and persecution and have access to prevention, treatment and care.
ICASO`s and AAE`s guiding principles:
- Central role of people, communities and their organizations in developing & implementing policies & programs;
- Right of community-based organization to determine its own priorities, methods of organization and programs, and to have those choices respected;
- Ensuring protection and fulfilment of human rights of all people living with, affected by, and vulnerable to HIV;
- GIPA principle: greater involvement of people living with,and affected by HIV;
- Ensuring that needs of women, young people and children are addressed, and that they are guaranteed an equal voice;
- Non-discrimination and non-stigmatization on the grounds of HIV status,gender, religion, race, sexual orientation,etc;
- Removing fear, coercion and deception from all programmes;
- Ensuring that relevant international programs involve partnerships among those living with and affected by HIV.
AAE’s core values: transparency, inclusiveness, MIPA (meaningful involvement of people living with HIV), a human rights based approach, networking culture and accountability. Our mission is communicated through websites, leaflets, work plans, annual reports.
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EURORDIS is a patient-driven alliance of Patient Organisations (POs) and individuals active in the field of rare diseases (RD). It represents the voice of an estimated 29 million citizens in the EU.

EURORDIS mission is to build a strong pan-European community of POs and People Living With RD (PLWRD), to be their voice at the European level and to fight against the impact of RD on their lives.

To this end, EURORDIS undertakes activities on behalf of its members, notably in favour of:

• Empowering RD patient groups
• Advocating RD as a public health priority
• Raising public awareness on RD (national and international levels)
• Improving access to information, treatment, care and support for PLWRD, including support to families
• Improving quality of life
• Encouraging good practices in relation to these issues
• Promoting scientific and clinical research on RD
• Developing treatments and drugs for people with RD

EURORDIS plays a pivotal role in the definition and implementation of the EU strategy on RD (EC Communication, Dec.2008 and Council Recommendations, June 2009).
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EPHA’s mission is to improve the health of all people living in Europe and to increase their participation in policy-making that affects their health.

Our vision is
- An equitable society where all individuals enjoy good health regardless of socio-economic status.
- Accountable and accessible EU institutions, transparent policy-making with real opportunities for input.
- Public health prioritized and mainstreamed across all policies, drawing on proven public health models and evidence-based population health interventions.
EPHA has a unique role as:
• A resource: Targeted and tailored information that empowers members and the wider public; a pool of collective expertise well-positioned to advise and evaluate.
• An advocate: An active, articulate champion of its core values that seeks constructive dialogue with institutions and policy makers; acts as a channel of communication to enhance the voices of the public health sector.
• A platform: A space for action, reflection and monitoring; a rallying point for public health groups in Europe; a network that stimulates genuine debate.

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