Summary
The COVID-19 Recovery Committee has published its report on Long Covid and post-Covid syndrome, urging the Scottish Government to take action to address the stigma surrounding the condition and improve awareness among the public and healthcare professionals.
The inquiry focussed on the awareness and recognition, therapy and rehabilitation, and study and research linked to Long Covid, with the Committee noting “concern” in their findings over reports of patients being unable to get the correct diagnosis and the lack of treatment for common conditions associated with the condition.
The Committee said it was “deeply saddened” to learn about the stigma faced by those with lived and living experience of Long Covid, and the report highlights the impact that the lack of awareness and recognition of Long Covid can have on those with the condition.
Content
The Committee recommended the Scottish Government:
- Works with the National Strategic Network and health boards to establish a single point of contact for Long Covid patients in every health board and develops standardised guidance.
- In partnership with the National Strategic Network, provide a leadership role in reviewing the best practice of Long Covid clinics and evaluate whether they may be an appropriate development in Scotland.
- Implement a public health campaign to raise awareness of Long Covid and the impact it can have on individuals' health and wellbeing.
- Reviews the current booster vaccination publicity strategy to reduce apathy and encourage uptake.
- Supports improving the integration of health boards and the third sector to provide self-management services for Long Covid.
Throughout the four-month inquiry, the Committee took evidence from a broad range of academics, clinicians and those living with Long Covid about the complex nature of the symptoms and the apparent lack of any lessons being learned from other chronic illnesses such as ME/CFS.
The Committee also made calls for more data on the prevalence of Long Covid to be gathered and noted the impact that incorrect coding of the condition can have on the accuracy of data, alongside encouraging improved use of data deployment into clinical practice.
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