If NICE recommendations change, how will the additional pumps and CGMs be funded?
The NHS is not exactly flush with money. I fear they will come at a cost to some other service.
I had relatives who worked in the NHS. I have friends who work in it now. It is a marvellous organisation.
However, many millions (billions) of pounds is wasted each year by the NHS. There are many efficiencies that could (and should) be made.
I bet cancer sufferers (and alas my family has, unfortunately, had run-ins with the "Big C") never say "
oh, I wonder where the NHS is going to find the money for this or that new cancer therapy."
The NHS still adopts a "pennywise, pound foolish" approach to diabetes. If (god forbid!) any of us have to have a limb amputated, or lose our eyesight, or our kidneys fail, or any one of a number of other quite horrible consequences of having this awful chronic disease befall us, in money-terms it will cost the NHS significantly more to treat those ongoing complications than handing out pumps and cgms to those that would benefit from it clinically.
Does anyone know how much it costs the NHS every time a diabetic is hospitalised with diabetic ketoacidosis? In 2017 the median cost for a hospital stay was put at £2064.
Yes the medical device companies are probably making a healthy profit margin (and I apologise for the part I have played in that over the years). But the NHS ought to have the negotiating nous to persuade these companies to offer it significant discounts IF the NHS can promise sufficient patient take up and use.
It is an unfortunate truth of life that if one let's others treat one terribly, or ignore one, human nature dictates that they will do so.
Adult diabetics pay tax. We deserve our money's worth! Don't we?!