Question to the Department of Health and Social Care:

To ask the Secretary of State for Health and Social Care, what steps he is taking to ensure the (a) timely and (b) consistent diagnosis and (c) treatment for people living with postural tachycardia syndrome.

We are investing in additional capacity to deliver appointments to help bring waiting lists and times down, including for those with postural tachycardia syndrome (PoTS). The Elective Reform Plan, published in January 2025, sets out the specific productivity and reform efforts needed to return to the constitutional standard, that 92% of patients to wait no longer than 18 weeks from Referral to Treatment, by March 2029.

Additionally, the shifts outlined in our 10-Year Health Plan will free up hospital-based consultants’ time by shifting care from hospitals to communities, utilising digital technology to reduce administrative burdens, and promoting prevention to reduce the onset and severity of conditions that lead to hospital admissions. This includes expanding community-based services, employing artificial intelligence for productivity, developing integrated neighbourhood health teams, and investing in digital tools and data. These shifts will allow specialists to focus on more complex cases of PoTS, enabling earlier identification and management, and improved patient outcomes.

By shifting care into the community through Neighbourhood Health Services, promoting integrated, multidisciplinary models of care and the expansion of personalised care plans, as outlined in the 10-Year Health Plan, we will ensure that people with conditions like PoTS receive more timely and accessible support closer to home.