Sweetbinty
Active Member
- Messages
- 41
- Type of diabetes
- Type 1
- Treatment type
- Insulin
Id like to know the cheapest way to get the sensors
I believe Superdrug sell them at £35 (I don't have one that's not a PITA to get to so can't confirm), I get mine from the Asda pharmacy near me for £44.
Yep £35 each and no you don't need a prescription, I know in Asda I do have to sign a form to get it VAT free - don't know what you'd have to do in SuperdrugIs this 35 each ?
Do you need a prescription ?
No, not Boots, certainly not my local one anyway. I've just got mine from Superdrug.I think Boots
don't know what you'd have to do in Superdrug
I've read a few that say no, and they are equally short sighted.
Hi, @Sweetbinty , like the others say, Superdrug seems to be ahead of the others at the moment pricewise, so maybe worthwhile making a few enquiries at any near you.
It's a postcode lottery at the moment on the prescription front. Many ccgs are citing lack of clinical data and seem to be playing a waiting game until formal data turns up.
I'm pretty sure one of the things they'll be watching is how it's playing out in other areas which have taken a more liberal approach.
Wales and Northern Ireland have been fine with it, and, like @Alison54321 , I'm fortunate enough to live in Edinburgh, where NHS Lothian decided to basically give it to any T1 who wanted it.
One of the interesting things which the consultant who led the short induction session I went to said was that they weren't that bothered about lack of clinical data, they just knew how hard T1 is to manage, if they were T1, they'd want it, so they couldn't in good faith deny it to us.
I suspect that he took that view because, despite lack of formal peer reviewed clinical data, the consultants were seeing so many libre self-funders on the ground at reviews saying, look, I'm paying for this myself, I'm more motivated, see how my a1c is down, with fewer hypos, see how the AGP graph I get from it tells me way more about what's going on than your basic a1c number does etc. etc...
I don't know how the NHS works (some parts of the NHS doesn't seem to know how it works either!) but I think self-funders can play a part in this by printing out their AGP graph and the various reports that libre can produce, taking them along to consultations, so that when the doc says, ok, your a1c is x, you can then say, ok, here's why, here's some graphs.
Docs like this stuff, they like seeing more information and seeing that patients are becoming more actively involved in management, so I think it does no harm at all for self-funders to do this.
It's bound to eventually filter down from the docs seeing us to the bean counters that it does make a difference, which will likely make a longer term saving in the costs of treating complications.
In Scotland, the Scottish Health Technologies Group is doing a report on it in June and some areas are hanging fire till that's out. I imagine there's similar things going on in England.
I think it's only a matter of time before ccg executives all over the country do a face-palm and say, duh, this is obvious, why didn't we fund this sooner.
Do you have an Asda nearby that has a pharmacy?Thanks all for your responses
Boots and superdrug do not do the sensors so its back to my drs and a costly bill monthly
It's not clear what the pathway of accountability is
I've given up trying to understand the politics of these things!
I work for a statutory body which is technically independent of the Government, but is funded by it, and has to report to it periodically, and it can statutorily change our rules of engagement.
What happens from time to time is that the Government is sitting there minding it's own business on a particular matter, then coal-face workers dealing with actual real live cases on the ground spot an issue X which will maybe have consequences Y if not dealt with, and then that input will either get dealt with internally, or might get escalated to a Minister's aide if it's a biggy.
Sometimes it's ignored, sometimes it's not, but I mention it because sometimes some subtle input from people dealing with real live cases can influence policy further up the decision chain.
I agree that there's a place for noising up MPs, provided it's articulate arguments, instead of green ink fury, but there's also a a place for subtle hints and nudges with those treating us on the ground.
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