Closed 21 events

England Rare Diseases Action Plan

The England Rare Diseases Action Plan, led by the Department of Health and Social Care, addresses diagnosis, treatment, and support for patients with rare and neglected diseases including haemophilia, Hansen's Disease, and Alpha-1 Antitrypsin Deficiency. The plan focuses on improving specialist access, research funding allocation, evidence availability, and equity across paediatric and adult services. The policy is active with ongoing parliamentary scrutiny of implementation and funding commitments.


Showing 21 key signals from 52 total
Family
Signal
Year
Body
Role

2026

4 events

2025

4 events

2024

3 events

2023

3 events

2022

2 events

2021

2 events

2020

1 event

2019

1 event

2018

1 event