Influencing national and EU policy-making through ... · • Setting the scene: Patient Evidence...
Transcript of Influencing national and EU policy-making through ... · • Setting the scene: Patient Evidence...
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Influencing national and EU policy-making through Partnerships & Alliances
Susanna [email protected]
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EFA 2015-2020Healthier
ENVIRONMENT
Quality of CARE
Patient
PARTICIPATION
INEQUALITIES
Europe where people with allergy, asthma and COPD:
• Have the right to the best quality of care and safe environment
• Live uncompromised lives
• Are actively involved in all decisions influencing their health
HEALTH IN ALL POLICIES
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EFA has its central office in Brussels, Belgium
Members
- 40 allergy, asthma and COPD patient organisations
- in 24 European countries
- Representing 500,000 patients in Europe
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EFA and its Members
→ Uniting patient groups at the EU level
→ Collaboration
→ Sharing knowledge & best practices
→ Capacity building
→ Tools/Facilitation for policy change
EFA Family, AGM 2015, Spain
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Patient movement development
• More organised (one voice)
• Credible, Equal partner
• From followers to leaders, but in different stages across the EU
• Only possible when partnership building has been done
• Nordic associations: leaders, Europe needs you!
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Rationale for partnerships• The whole chain of care patient centred – work
with all healthcare professionals (HCPs)• Integration of prevention into care and all
policies – work with environment/tobacco/health NGOs
• Ownership• Maximise impact, but don’t dilute patient
perspective• Let those lead whose core business its all about -
> patients to lead on patient centred care!• Patient groups together: strong voice, shared
priorities
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EFA Partnerships
EFA
Care
Environment/Risk factors
Inequalities
Participation
- Health Care Prof Groups in allergy & respiratory- Patient Groups
- Health & Environment Alliance- European Network for Tobacco- Public Health NGOs
New objective!- Cross cutting in all partnerships
- Patient Groups- Research Community
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Working with Members• Advocacy tools:
• Setting the scene: Patient Evidence and Best practise
• EU legislation: from Briefing, Consultation, Joint position into Template letters to MEPs/Council, Summary of results, Supporting patient involvement in implementation
• Methods • Working groups: patient education, health
determinants, allergy, asthma, COPD
• Training: Annual Meet & Greet the EU Institutions
• Capacity building project
• Translations
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EPF
• Our key partner:• Brings us together with other chronic disease patient
groups
• Leads on issues common to all patients and decided at EU level: Medical Devices and Clinical Trials legislations, Patient Safety….
• Shares important policy developments
• Provides easy opportunities for advocacy
• Builds our capacity
• Saves our resources
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National Alliances/Platforms of Patients
• Building one united patient voice
• Solidarity across diseases to achieve access to & quality of care
• Share common issues, concentrate on your disease specific issues
• When one patient voice is invited, all will be represented• Health care policy
• Patient participation
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European ‘Patients Policy’
Regional/Local
Policy
National
Policy
National/
EU PolicyEU Policy
European
Patients’
Forum
National Platforms of Patient Groups
Disease Specific
Patient Group
European Level Disease Specific Patient Groups
Disease Specific
Patient Group
UNIFIED MESSAGES – SOLIDARITY ACROSS DISEASES – PATIENT POWER
EU POLICY IN SUPPORT OF NATIONAL POLICY – NATIONAL POLICY INFORMING EU POLICY
Local patient groups
Local patient groups
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TACK – TAK – TAKK - ÞAKKA ÞÉR - KIITOS.
European Federation of Allergy and Airways Diseases Patients’ Associations35, rue du Congrès
B-1000, Brusselswww.efanet.org@EFA_Patients
www.facebook.com/EFAPatients
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PATIENTS & SCIENTISTS IN ACTION!
with Keith Taylor, MEP at the EP