| Heading: |
Chronic Fatigue Syndrome: Wiltshire |
| Question ID: |
1812627 |
| UIN: |
59887 |
| House: |
Commons |
| Date tabled: |
2025-06-13 |
| Asking Member ID: |
5239 |
| Asking Member display name: |
Sarah Gibson
|
| Asking Member handle: |
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| Asking Member Twitter reference: |
Sarah Gibson
|
| Member interest: |
false |
| Question text: |
To ask the Secretary of State for Health and Social Care, what steps his Department is taking to improve the diagnosis of myalgic encephalomyelitis in primary care settings in Wiltshire. |
| Is named day: |
false |
| Date of holding answer: |
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| Date answered: |
2025-06-23 |
| Date answer corrected: |
|
| Is holding answer: |
false |
| Is correcting answer: |
false |
| Answering Member ID: |
4981 |
| Answering Member display name: |
Ashley Dalton
|
| Answering Member handle: |
AshleyDalton_MP
|
| Answering Member Twitter reference: |
@AshleyDalton_MP
|
| Correcting Member ID: |
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| Correcting Member display name: |
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| Correcting Member handle: |
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| Correcting Member Twitter reference: |
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| Answer text: |
Integrated care boards (ICBs) are responsible for commissioning specialist myalgic encephalomyelitis, also known as chronic fatigue syndrome (ME/CFS), services that meet the needs of their population, subject to local prioritisation and funding. The proce... |
| Original answer text: |
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| Comparable answer text: |
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| Answering body ID: |
17 |
| Answering body name: |
Department of Health and Social Care |
| Tweeted: |
true |