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  • About us
    • What we do
    • Our team
    • Our trustees
    • Our strategy
    • Contact us
  • Our members
    • Search our members
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  • News
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    • Reproductive options
    • Diagnosis
    • Medical research
    • Healthcare and delivery
    • Access to treatment
    • Living and education
  • Information
    • Living with a genetic condition
    • Learn about genetics
    • Services and testing
    • Research and innovation
  • Get involved
    • Join our team
    • Join our mailing list
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    • Be a corporate partner
      • Ways to get involved
      • Our current corporate partners
      • Working with industry policy
      • Ethical collaboration policy
    • Leave a gift in your will
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Healthcare and delivery

We work on a variety of issues that families and individuals with genetic conditions face. We aim to provide information, support families and influence the services needed by these patients. We also work to add patient voice into debates that matter to our community. Our work falls into different categories:  reproductive techniques, diagnosis, medical research, healthcare and delivery, access to treatments and living and education.

  • Reproductive Options
  • Diagnosis
  • Medical Research
  • Healthcare and Delivery
  • Access To Treatment
  • Living and Education
Response to the Caldicott Review
Policy

Response to the Caldicott Review

Proposals to display medicines pricing on packaging
Policy

Proposals to display medicines pricing on packaging

Brexit: the impact on rare disease
Policy

Brexit: the impact on rare disease

The benefits of EU membership for our community
Policy

The benefits of EU membership for our community

HTA codes of practice consultation

Setting the mandate to NHS England for 2016 to 2017
Policy

Setting the mandate to NHS England for 2016 to 2017

Our response to the Maternity Review
Policy

Our response to the Maternity Review

Children and young people’s continuing care framework

The value of secondary use of data in Northern Ireland
Parliamentary

The value of secondary use of data in Northern Ireland

Models of consent for NCARDRS
Policy

Models of consent for NCARDRS

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  • NHS Genetic Services in the UK
  • What is a genetic test?
  • Finding information about my condition
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  • NHS Genetic Services in the UK
  • What is a genetic test?
  • Finding information about my condition
  • Finding a support group
Genetic Alliance UK provides the secretariat for the following parliamentary groups on Rare, Genetic and Undiagnosed Conditions:
  • Westminster APPG
  • Welsh CPG
  • Scottish CPG
  • Westminster APPG
  • Welsh CPG
  • Scottish CPG
  • Ethical Collaboration Policy
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  • Working With Life-sciences Industries Policy
  • Disclaimer
  • Ethical Collaboration Policy
  • Privacy Policy
  • Donation Policy
  • Complaints Policy
  • Working With Life-sciences Industries Policy
  • Disclaimer

© Genetic Alliance UK 2021
Registered charity numbers: 1114195 & SC039299. Registered company number: 05772999

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