1 1  key values social justice, empowerment, solidarity, activism, independence and balance (e.g. between service delivery and advocacy)  NGO created.

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Presentation transcript:

1 1  key values social justice, empowerment, solidarity, activism, independence and balance (e.g. between service delivery and advocacy)  NGO created in France in 1981 – currently 15 autonomous associations (Argentina, Belgium, Canada, France, Germany, Greece, Japan, Netherlands, Luxemburg, Portugal, Spain, Sweden, Switzerland, UK, USA)  access to healthcare through freely accessible frontline medical services 316 programmes in 78 countries (in 2013)  Among these, 170 are domestic programmes in 15 countries  Volunteer-centered organization (e.g. over health professionals across domestic programs) Doctors of the World – Médecins du monde Our values and identity

2 2  domestic programs: homeless people, asylum seekers, Roma communities, elderly, destitute EU citizens or nationals and third-country undocumented migrants, drug users, sex workers  20% of our national programs are healthcare centers (with referrals to mainstream healthcare whenever possible) + vast majority of mobile units & outreach  harm reduction approach, empowerment of smaller organizations and supporting the creation of self-support groups  data collection on the social determinants of health and patients’ state of health as a basis for our advocacy: evidence based… Doctors of the World – Médecins du monde Who we are and what we do

3 3  Urging MS & EU institutions to ensure universal public health systems built on solidarity, equality and equity, open to everyone living in a European member state  Focus on children (esp. universal vaccination coverage), ante- and postnatal care, coherent infectious disease policies without exclusion (HIV, hepatitis, TB) – advocacy rooted in field experience (we only speak about what we see; only those with first-hand experience speak)  Protection of seriously ill migrants from deportation to countries without effective access to healthcare  e.g. regular contacts with DG SANCO, ECDC, FRA or CoE institutions, participation to EP hearings, partnerships with PICUM and EPHA, partnerships with health professionals Doctors of the World – Médecins du monde Common advocacy towards EU institutions

Additional focus points: (psycho)social counselling – Training / education – Health and sexuality education – Peer education – Continuity of care for migrants in detention – Legal & integration assistance for migrants (including interpretation) - Influencing migration policies – Community mental health interventions – Harm reduction – Public health research / social epidemiology

SERVICE DELIVERY

EXPERTS Working with interpreters, mediators, peer workers: MdM DE, Czech Consortium (CZ), BFPA (BG) Volunteers: MdM DE & NL, Menedék (HU) Violence faced by service users: INSERM (FR) Mental healthcare: INSERM (FR), MdM DE & PT, Health centre UDM (NO) HIV/HCV & HBV: INSERM (FR), MdM PT Sexual & reproductive care: BFPA (BG) Pediatric care: MdM DE Harm reduction drug use: MdM FR, DE and CA Harm reduction sex work: MdM FR Funding strategies: MdM DE

EXPERTS – Czech Consortium (CZ) on how to involve service users in a programme

EXPERTS on DATA COLLECTION Testimonies & case studies: C-HM (AT), Czech Consortium (CZ), MRCI (IE) Audiovisual productions: MRCI (IE) Legal analysis: MdM DE, C-HM (AT) Quanti: INSERM (FR) and C-HM (AT), MdM DE, Menedék (HU) Quali: INSERM (FR) and C-HM (AT), Menedék (HU)

EXPERTS on ADVOCACY Working with health professionals: MdM DE & NL Working with academics: INSERM (FR), Czech Consortium (CZ) Action plan & objectives: MdM SE

11  Mutual learning on how to improve service delivery, e.g. group training sessions, 1-to-1 peer review process (2016-’17) + identifying similar partners in other EU countries (at least 5 new every year)  (Mutual) learning on empowerment (e.g. workshop with grass-root organization representatives and peer workers)  Common data collection (testimonies & case studies / legal analysis / common routine quantitative data collection if possible, short surveys if possible)  e.g. 10/2015 Paris workshop on quantitative data collection  Common advocacy towards EU institutions (and mutual learning on how to successfully advocate for social change), e.g. common yearly publication, Brussels EP dissemination event (2016), high-level EC event (2017), common outreach towards health professionals and academics The European Network to reduce vulnerabilities in health PROPOSED WORKPLAN