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🧵/ The NHS is about to undergo one of the most radical – and scandalous - changes in its history. From 1st April (the public are the fools in this), GPs will be contractually obliged to seek remote “advice & guidance” from hospital clinicians, making it even harder to see an NHS specialist.

Does this sound part of a plan to genuinely ‘fix’ the NHS, as Wes Streeting vowed he would do when taking up office - or more like a tactic to ration hospital care by overriding GPs in order to massage the waiting list figures? It is, of course, the latter, an extra layer of bureaucracy...

..that at best will delay patients’ access to the specialist treatment they need, at worse sacrifice those patients on the altar of fake news about “falling” waiting lists. You don’t need me to point out the potential patient safety risks. We all know that time, in medicine, can be everything..

..The Royal College of GPs has been crystal clear: “The use of advice and guidance should not be mandated in any area… We have heard reports of risks of delays, with tests being required before any referral, lost messages and staff without appropriate senior clinical oversight handling requests.”..

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..The aim, says the Times, is to reduce the number of hospital outpatient appointments by 30 million p/a. And the government, in a quite breathtaking example of political spin, is presenting this as “good” for patients - as though all those people who’ve been waiting months or even years..

I’ve been waiting ten months for a urology appointment and had watched on the app and then a couple of weeks ago everything on the app my waiting list section had disappeared. OH pestered me to ring department to be told I’d dropped off the waiting list although they booked me in because I’d called.

..for the first Rheumatology, Neurology or Orthopaedics appointment they so desperately need are just, you know, malingering. (I recently spoke to a patient with a new diagnosis of multiple sclerosis who’d been waiting over six months to see a neurologist for the first time – simply scandalous.)..

I was diagnosed with severe osteoporosis 18 months ago. I never saw a consultant . However I did have excellent care from the rheumatology people in Oxford , state of the art medication and a swift handover to my GP at the end of it. Apart from some dodgy admin I was very happy. Was I wrong?

Isn't this already happening by default. Both my kids have been refused multiple referrals as "we don't diagnose that" leaving the GP floundering and just treating what they think it might be.

I believe this is a national health scandal from a govt that apparently cares more about good spin than it does about good patient care. If you feel the same, please – please – write to your MP & tell them why. Please shout about this online, anywhere you can. Don’t let this slide. Thank you.

The only real solution is a increasing in spending on PPP per capita basis. Rather than GDP per capita as some new organisations have misrepresented other countries as spending less, but getting more from that amount.