I would be perfectly happy to pay more tax for the NHS if I felt it would extrapolate into higher quality and better service. Regrettably I don't think it will because too many people in the NHS think they are doing the public a favour and we should be grateful for the sub-optimal and all too often inaccessible care.
When DD was ill with her MH there was no help available on the NHS for a 15 year old who was cutting, restricting food and taking overdoses. The GP blamed CAMHS, CAMHS blamed the CCG and the government, the CCG blamed CAMHS, the GP and the government. One GP actually told me to get her a therapist off the Internet because CAMHS were useless. Not great in front of a 15 year old who had reached out for help. My tax statement tells me how much is paid to the NHS; it does not tell me that it no longer funds mh services for children and young people. I later found out that the year before the CCG had not paid its quota for CAMHS to the MH Trust. GPs sit on the CCG board, yet despite knowing that quota had not been paid happily told people CAMHS were useless and they couldn't refer to any private providers.
The system absolutely stinks and the one time we did need the NHS it failed us. Thank goodness for BUPA and the ability to fund the enormous amount of therapy required and the assessments for ASD/ADHD. All masked due to a high functioning child from a loving and supportive home.
The NHS needs root and branch reform and if GPS can't service the number of patients registering they need to stop registering them. Only then will the shortfall be recognised and dealt with.
As I have said before 30 years ago I needed one prescription per year for levothyroxine. Now with 56 day prescribing I need 6. I would venture that much of the problem is that GPs make work for themselves by going along with these silly initiatives and that is where my patience begins to cease.
The system needs to change.