For years and years I thought the fact that my need for levothyroxine meant that I got other prescriptions free was nuts too. And it was when all I needed was a whisper of HRT or a course of antibiotics every seven years.
And then I developed osteoporosis most likely because a GP failed to diagnose graves disease for about five years in my 20s. In the last few months I've needed the following prescriptions:
Risedronate x 2
Adcal x 2
HRT x 3
Cocodamol x 2
Omeprazole x 2
naproxen x 2
laxatives x 1
Levothyroxine x 2
That totals £128. Likely to need many of those meds for years to come too although if the omeprazole is long term I'll need bisphosphonates via an effusion because it stops the latter working. I might not have osteoporosis had the graves been diagnosed. I might not have a wedge fracture of my spine if I hadn't got the osteoporosis. I therefore no longer think the free prescription issue is nuts.
Yes, I could easily afford those prescriptions but why should I when my family as top 1% earners and tax payers already pays shedloads into the NHS which sadly has not provided us with too great a service in the last six months.
No treatment via CAMHS for dd so we have paid for that in spite of what we have already contributed.
GP didn't want to refer my back problem under the NHS so privately I've had a consultation, further Xrays and an MRI and advised I need a surgical procedure to help rebuild a vertebrae. Needs doing within 8 weeks of the break to be really effective but GP didn't want to contemplate referring until at least 10 weeks after so never mind developing chronic long term back problems. So that's another several thousand out of my pocket as well as the NHS contributions.
I have no doubt I'll end up paying for the effusions and rheumatology referrals too.
So, you see I really don't accept that I should pay extra on top of what I already pay for a service that appears to be non existent. If I don't get my problem treated it is likely that I might not be able to work until retirement and the NHS misses out on further tax contributions from me.
The NHS has not served my family well at all in the last six months. My trip to a&e met with a bunch of jobsworths (the doctors were absolutely fine btw) but the reception staff were monumentally rude to all they dealt with and the nurse I dealt with was the ultimate jobsworth. Both refused to help me find a suitable seat with a broken back and told me to stand and wait if I couldn't sit in the low metal chairs provided.
The only positive I can think of if I had been sent a further bill for that visit to a&e is that I would been delighted to return the invoice with a letter of complaint directly to the chief executive.
I thought the aim of the NHS was equal access for all. Charging those who pay the most more is hardly equal.
Current bill for necessary treatment not available via the NHS to ensure members of my family fulfil their potential and continue contributing is I think about £12,000. If people like us are prevented from contributing because we are not optimally treated to keep us working then that will result in a totally and permanently fucked NHS.
And finally, as a society we spend millions training nurses. We should be insisting that nurses continue to do what they were trained to do and that is to nurse. They weren't trained to manage and they don't make good managers - ask some doctors. They needs to be back on the wards, working and nursing. Personally when I do use the NHS I generally find that I get an exceptionally good service from the doctors I come across. I do not get an exceptionally good service from the nurses or from the administration I deal with. Invariably they are uncaring and have a air of doing the patient a favour. Too often their actual role and training is opaque and it is very hard to work out if one is dealing with a nurse or a healthcare assistant. It is never clear. It is not good enough.