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  • Rare Reach Festival
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  • Rare Reach Festival
    • People’s Choice Vote
    • Best storytelling by a large charity
    • Best storytelling by a small charity
    • Best storytelling by a voluntary group
    • Best storytelling by a family member
    • Best storytelling by an individual
    • Best storytelling by a young person
  • What is a rare disease?
  • Our Work
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Patient Experience

All of the work Rare Disease UK does is based on what we hear from our community and the experiences of people living with rare, genetic and undiagnosed conditions. See below for how we incorporate patient experiences into our work, from written reports to parliamentary events.

  • Coordination of Care
  • Diagnosis
  • Patient Empowerment
  • Patient Experience
  • Research
Patient Experience

Rare Disease Day 2021: Virtual Parliamentary Event

rare-diseaseday-2019-img-3
Patient Experience

Rare Disease Day (2019)

Patient Experience

Illuminating the rare reality (2019)

Diagnosis

Why England needs an implementation plan for the UK Strategy for Rare Diseases (2017)

Patient Experience

Rare Disease Day 2017

Diagnosis

Implementation of the UK Strategy for Rare Diseases in England

Diagnosis

Patient Empowerment Group

Coordination of Care

The Rare Reality (2016)

Rare Disease Transition image
Coordination of Care

Patient Experiences of Transition Between Care Providers (2014)

Patient Experience

Rare Disease Care Coordination (2013)

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About Rare Disease UK
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  • How do I find information about my condition?
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  • How do I find information about my condition?
  • How do I find a support group?
Genetic Alliance UK provides the secretariat for the following parliamentary groups on Rare, Genetic and Undiagnosed Conditions:
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  • Ethical Collaboration Policy
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  • Working With Industry Policy
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© Genetic Alliance UK 2021
Genetic Alliance UK registered charity numbers: 1114195 & SC039299. Registered company number: 05772999

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