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Chamber and committees

Question reference: S7W-02862

  • Asked by: Maggie Chapman, MSP for North East Scotland, Scottish Green Party
  • Date lodged: 3 September 2026
  • Current status: Answered by Maree Todd on 15 September 2026

Question

To ask the Scottish Government what it is doing to support the diagnosis, treatment and care of individuals with Ehlers-Danlos syndrome (EDS) and Hypermobility Spectrum Disorders (HSD) in NHS (a) Grampian and (b) Tayside.


Answer

Through Scotland’s Rare Disease Action Plan, we are taking forward actions to improve support for people with Ehlers-Danlos syndromes (EDS) and related conditions, including hypermobility spectrum disorders (HSD). This includes work to support earlier diagnosis, increase awareness among healthcare professionals, and improve coordination of care and access to services. The Rare Disease Action Plan Progress Report, published on 27 February 2026, provides an update on progress to date.

While the Scottish Government sets the strategic policy direction for the NHS in Scotland, the delivery of healthcare services is the responsibility of local NHS Health Boards, in line with national guidance and population needs.