Written question asked by Tom Morrison (Liberal Democrat) on Friday, 26 June 2026, in the House of Commons. It was due for an answer on Tuesday, 30 June 2026. It was answered by Sharon Hodgson (Labour) on Monday, 6 July 2026 on behalf of the Department of Health and Social Care.
ME/CFS: Health Education
- Question
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To ask the Secretary of State for Health and Social Care, how people with lived experience of ME/CFS will be involved in the design and delivery of the awareness campaign.
- Answer
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Lived experience had an integral role during the development of the final myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) delivery plan. The awareness plan will also require continued support from people with lived experience, and the ME/CFS community, for the distribution and promotion of any materials produced. The campaign will aim to focus on capturing attention and delivering key messages, which will then serve as a gateway to finding more information.
Departmental officials are currently considering how to involve people with lived experience of ME/CFS in the design and delivery of the ME/CFS awareness campaign, in addition to also exploring options for the format of the awareness campaign.
Secondary information
- Type
- Written question
- Reference
- 13623
- Session
- 2026-27
- Subjects
- ME/CFS Health education
- Link
- View this Written question on www.parliament.uk
Librarians' tools
- Timestamp
- 2026-07-06 12:17:45 +0100
- URI
- http://data.parliament.uk/writtenparliamentaryquestion/commons/2026-27/13623
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- http://indexing.parliament.uk/Content/Edit/1?uri=http://data.parliament.uk/writtenparliamentaryquestion/commons/2026-27/13623
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- https://search.parliament.uk/claw/solr/?id=http://data.parliament.uk/writtenparliamentaryquestion/commons/2026-27/13623