Hi Jo. Just noticed that you live in Australia. I don’t know what diabetes care is like there, but can say there appear to be differences around this country.
I move around a lot because of my work. Originally (mis)diagnosed in London, where diabetes care was great (at least with my practice). After the misdiagnosis was discovered, they checked there records and found I wasn’t the only one – the nurse went for further training! Moved to Devon and diagnosed again (properly this time). Care less good. One locum wanted me on Metformin, BP meds and statins. We agreed to disagree. (I cannot take statins and had no desire to take Metformin- I react badly to some other drugs and didn’t even want to contemplate that one). Another move, to Cornwall. Similar conversations again.
Then up to northeast England, near Newcastle. At least there they gave me testing supplies on prescription, like London but unlike Devon and Cornwall. Well, they did for a few months. Then stopped for financial reasons.
Yet another move, to near Durham. Only one doctor’s surgery in the village, so no choice. Not seen the doctor since I arrived June 2015. Diabetes care by nurse. One visit she’s all for the BSD, another visit she’s not. With her colleague sitting in they said this was not sustainable. Wanted me on Metformin and statins. Yet again said I can’t take statins – they don’t agree with me! I’ve even offered to go to speak to the doctor about the BSD, or to talk to a group of diabetics. No answer.
The NHS wants us to be proactive in our care, but doesn’t give us the tools. While some prescribe testing strips, many don’t. And not everyone can afford to buy them. And most medics still seem to be telling diabetics to eat carbs at every meal. There have been reports that overweight diabetics are going to be referred for bariatric surgery so they will lose weight and ‘reverse’ their diabetes. At a cost of several thousand pounds per patient. But, guess what, they have to go on a low cal diet prior to surgery to lose fat from their livers. Errrr …….?
On the brighter side – we have a local Health Educator who met me when I had just started the BSD. Next time we met she nearly didn’t recognise me. She spoke to one of my groups about healthy eating – the party line on carbs (I had to glue my mouth shut!). She agrees with what we are doing, but couldn’t say that officially! Next year she’s hoping to be able to speak more openly about low-carbing.
Others may have different, better, experiences but these are my personal experiences. I hope the system and treatment in Australia (and other countries) is better than here.
Sorry for the rant, but all we seem to hear is that diabetics are to blame for the funding crisis in NHS. One GP said they would bankrupt the NHS! Yet they are spending (wasting) so much money on treatments that could be avoided (or at least reduced). I wonder just how much money those of us on here have saved the system? I get so frustrated – so apologies again!