Submitted on Tuesday 7th January 2025
Rejected on Friday 28th February 2025
Current status: Rejected
Rejection code: duplicate (see below for details)
Improve services for those living with Postural Tachycardia Syndrome
Calling on Parliament to urge the Government to instruct the NHS to form specialist services, guidelines, training resources and a clinical pathway for the diagnosis and treatment of patients with symptoms of PoTS and related autonomic nervous system dysfunction (dysautonomia) in every region.
PoTS is a common, long term, debilitating health condition which mostly affects young people. 90% will improve with access to treatment, but due to the lack of recognition of symptoms and access to healthcare, the average time from onset to diagnosis is 7 years. Many patients throughout the UK currently have very restricted or no access to specialist NHS healthcare as many regions have no specialist services, and there are no clinical care pathways in the UK, and no UK medical guidelines.
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The Government e-Petitions Team gave the following reason:
There's already a petition about this issue. We cannot accept a new petition when we already have one about a very similar issue.
You are more likely to get action on this issue if you sign and share a single petition.
You may wish to sign the following petition, which calls for similar action:
Postural Tachycardia Syndrome: fund training and facilities
petition.parliament.uk/petitions/706884
18.220.89.112 Sat, 01 Mar 2025 00:14:01 +0000
