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Written question asked by Scott Arthur (Labour) on Monday, 29 June 2026, in the House of Commons. It was due for an answer on Wednesday, 1 July 2026. It was answered by Preet Kaur Gill (Labour) on Wednesday, 8 July 2026 on behalf of the Department of Health and Social Care.


Musculoskeletal Disorders

Question

To ask the Secretary of State for Health and Social Care, what steps his Department is taking to increase awareness of Inclusion Body Myositis and other rare progressive muscle disorders.

Answer

The Government remains committed to improving outcomes for people living with rare diseases, including inclusion body myositis and other rare progressive muscle disorders, through the UK Rare Diseases Framework and successive England Rare Diseases Action Plans. Increasing awareness among healthcare professionals is one of the framework’s four priorities.

As set out in the 2026 England Rare Diseases Action Plan, NHS England continues to expand rare disease education through the National Genomics Education Programme, including GeNotes, a clinical resource that now covers more than 150 rare diseases and has been integrated into primary care decision-support tools used by general practitioners. NHS England is also developing resources to support healthcare professionals in having sensitive conversations with patients receiving a rare disease diagnosis, while the Genomics Training Academy provides education and training to the specialist genomics workforce.

These initiatives support earlier recognition, diagnosis, and appropriate management of rare conditions.


Secondary information

Type
Written question
Reference
14179
Session
2026-27
Subjects
Musculoskeletal disorders Rare diseases
Link
View this Written question on www.parliament.uk