an introduction to genetic alliance uk’s work in scotland natalie frankish – development officer...
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An Introduction to Genetic Alliance UK’sWork in ScotlandNatalie Frankish – Development Officer for Scotland
Event: Action DuchenneScottish Conference
Date: 4TH December 2015 12noon - 5pm
• Genetic Alliance UK is the national charity working to improve the lives of patients and families affected by all types of genetic conditions.
• We are an alliance of over 180 patient organisations.
• Our aim is to ensure that high quality services, information and support are provided to all.
• We actively support research and innovation across the field of genetic medicine.
Genetic Alliance UK
Our Mission three main elements:
• Supporting:We seek to raise awareness of genetic conditions and improve the quality of services and information available to patients and families.
• Campaigning:We actively campaign on behalf of those with genetic conditions on issues of policy and practice to influence governments, policy makers, industry and care providers such as the National Health Service.
• Uniting:We provide a united voice for all those affected by genetic conditions, enabling us to work together towards a common goal of making life better for patients and families at risk.
Genetic Alliance UK
• Since 2005
• Devolution of Health – Scottish Political landscape
• Development Officer for Scotland
• Funded through Scottish Government (Calman Review, Strategic Funding Partnership)
• Varied role – policy, public affairs, development, patient engagement, member relations
Genetic Alliance UK – Scotland
Development Officer for Scotland
• In post since 2010• Policy and engagement
background• Responsible for our work in
Scotland• Key areas of work
• Policy• Virtual Patient Panel• Genetic Alliance UK & Rare
Disease UK
• Rare Diseases defined by the European Union as one that affects less than 5 in 10,000 of the general population.
• 6,000 – 8,000 known rare diseases.• 1 in 17 people will be affected.• 300,000 people affected in Scotland – 3.5m in
UK• Collectively, rare diseases are not rare at all.• In the UK, a single rare disease may affect up to
about 30,000 people. • Duchenne Muscular Dystrophy is a rare disease.
Rare Disease
• An initiative of Genetic Alliance UK. • Formed in Nov 2008 - following the publication of the
European Commission’s Communication on Rare Diseases.
• Since then, RDUK has been the National Alliance for people with rare diseases and all who support them.
• Rare Disease UK is open to anyone with an interest in rare diseases and includes patients, family members, patient organisations, clinicians, researchers, academics and industry.
• Overlap between the work of Genetic Alliance UK and Rare Disease UK – with approximately 80% of rare diseases having a genetic component.
Rare Disease UK
Rare Disease UK
Key Campaigns:
• Strategy for Rare Diseases Improving Lives, Optimising Resources: A vision for the UK
Strategy for Rare Diseases Involved in developing UK Strategy Consultation on Scottish Implementation Plan Scottish Government Oversight Implementation Group
• Access to Medicines for Rare Diseases Public Petition campaign to improve access to medicines for rare
disease patients in Scotland
Rare Diseases in Scotland
• UK Strategy for Rare Diseases – Nov 2013
• Home Nations to launch Implementation Plans
• Scotland first to develop – consulted with RDUK
• Launched Plan in July 2014
• Recognises that the delivery of the commitments of the UK Strategy in Scotland needs collaborative working between the NHS, public and third sector, partners, researchers, academic institutions and industry.
• Plan outlines the key objectives, in relation to the 51 commitments of the UK Strategy.
Scottish Plan for Rare Diseases
• Patient Empowerment Opportunities for patients to be involved in decision making on all
levels Access to registries and patient information
• Identifying and Preventing Registries Screening
• Diagnosis and Early Intervention Patient Pathways Databases Training
• Co-ordination of Care Patient Pathways
• Research Support research through role of CSO UK Rare Genetic Disease Research Consortium Agreement.
Scottish Plan for Rare Diseases
• Access to medicines for rare diseases can be very difficult• Scottish campaign – Scottish Parliament Public Petition• Health and Social Committee Inquiry & Scottish Government
Review• Recommendations
SMC • Greater transparency and patient engagement• Processes for orphan and ultra-orphan medicines
IPTRs• No more exceptionality• To be replaced by Peer Approved Clinical System
New Medicines Fund• £90 million ring-fenced for rare and end of life medicines
Access to Medicines
• Recent success with Translarna – IPTR process• SMC Appraisal – PACE
• SMC Review • Genetic Alliance UK continues role with SMC
• Patient Charter on Access to Medicines for Rare Diseases (Scotland) Recommendations for further improvement Patient engagement throughout process key Input from Action Duchenne
Access to Medicines
Transitions
Difficulties reported by members.
Survey of patients
Key findings: • Good communication & coordination essential• Patients and families feel disconnected• Age appropriate services not always available• Transition can be a shock and stressful• Patients feel unsupported throughout• Transition is better for more common conditions• Research not compatible with research• Need for dedicated transition services
Scottish Muscle Network
• Virtual Patient Panel Online network for patients – anyone can join Find out news, give feedback, share experiences Can be involved as little or as much as you like Sign up with me
• Rare Disease Day 2016 Join us in the Scottish Parliament – 1st March 2016 Attend our National Conversation events in March Tell me about your activities
• Cross Party Group on Rare Diseases Raising awareness of Rare Diseases in Parliament
Get involved in our work
