The other thing is how suitable for me it really is.
I have a couple of ways I could fund it. But I have not been able to get anyone medical to sign off on it... and the amazingly super awesome people who are offering to help fund it want that to happen before we can actually do it. So I asked loads but it was always "well let's wait and see how we're doing shall we?"
(I love that "we" thing they do, like my **** body is going to make their toes fall off... I wish...)
But the point is, I get the feeling there are basically two groups of people who aren't allowed to have it people who are so awesome they don't need it, which is definitely not me, and people who are so **** it wouldn't help which I fear is very much me. But the thing is that between those groups is a really narrow band of people they will probably allow to have it, no matter how they fund it. I could probably just pay for it, even, but I have no idea what anyone's attitude to that would be.
The first and most important thing to learn about diabetes is that it's yours so do whatever you want with it. Use the internet and journals, read about stuff, then if you think it will benefit you, based on the evidence available, just do it. I've, by hook or by crook, got hold of various diabetes treatments that either you can't get in the UK, you can't get on prescription for Type 1 under NICE guidelines to see what the effects would be, or that the esteemed medical profession decided it didn't want me to have, but I found anyway (med devices included). Given the Abbott Libre is none of these, and is a freely available retail product, why wouldn't you do it if you can afford it? Yes, to get it funded the very cool people who are offering to fund it may need additional medical sign off, but if you can and you can afford to, why wouldn't you?The other thing is how suitable for me it really is.
I have a couple of ways I could fund it. But I have not been able to get anyone medical to sign off on it... and the amazingly super awesome people who are offering to help fund it want that to happen before we can actually do it. So I asked loads but it was always "well let's wait and see how we're doing shall we?"
(I love that "we" thing they do, like my **** body is going to make their toes fall off... I wish...)
But the point is, I get the feeling there are basically two groups of people who aren't allowed to have it people who are so awesome they don't need it, which is definitely not me, and people who are so **** it wouldn't help which I fear is very much me. But the thing is that between those groups is a really narrow band of people they will probably allow to have it, no matter how they fund it. I could probably just pay for it, even, but I have no idea what anyone's attitude to that would be.
Feedback from my work colleague on Wednesday after he's been to the course tomorrow should make it clearer. Actually our other T1 in the office has told me she's going to a training session too.
We don't know if they've been selected because of some underlying facts specific to them eg a1c, general control issues, but the wording of the announcement kinda suggests they're basically inviting every T1 in Lothian along in batches - I'm still waiting for my letter.
I wouldn't imagine they'd invite people along to a course just to tell them they're not going tp get it, but, like I say, I just don't know at the moment whether those who get letters have been chosen because of underlying issues or whether it's a more general roll out.
Should be clearer on Wednesday once I hear back from them.
My DN last week said I was "borderline obsessive" for being a T2 who tests their bloods, sometimes, 4 times a day and that, if I were still testing to that degree at my next appointment in July (and was foolish enough to tell her about it), she'd refer me for psychiatric support.
So, yeah, medical professionals do think testing more regularly is a bad thing.
I am in Lothian also and received a letter at the weekend. I believe I fit the eligibility criteria, and will be going on the training session in March. (Eligibility criteria are on MDI or pump, and have been on DAFNE or similar, and agree to share info with HCPs).
@Scott-C . Things looking good. Hope you get the prescription.
I can take 50 quid off your hands if you're struggling ( cash or cheques) each month..
The other thing is how suitable for me it really is.
I have a couple of ways I could fund it. But I have not been able to get anyone medical to sign off on it... and the amazingly super awesome people who are offering to help fund it want that to happen before we can actually do it. So I asked loads but it was always "well let's wait and see how we're doing shall we?"
(I love that "we" thing they do, like my **** body is going to make their toes fall off... I wish...)
But the point is, I get the feeling there are basically two groups of people who aren't allowed to have it people who are so awesome they don't need it, which is definitely not me, and people who are so **** it wouldn't help which I fear is very much me. But the thing is that between those groups is a really narrow band of people they will probably allow to have it, no matter how they fund it. I could probably just pay for it, even, but I have no idea what anyone's attitude to that would be.
I test a lot more than six times a day, does that make me an idiot or a weirdo because it must be one of the other...
I test a lot more than six times a day, does that make me an idiot or a weirdo because it must be one of the other...
to get it funded the very cool people who are offering to fund it may need additional medical sign off, but if you can and you can afford to, why wouldn't you?
It might be worth gritting your teeth and going - you can hopefully get your insulin changed too xBecause that would mean going to see the SHUDDER clinic, and I am barely on speaking terms with them.
I am in Lothian also and received a letter at the weekend. I believe I fit the eligibility criteria, and will be going on the training session in March. (Eligibility criteria are on MDI or pump, and have been on DAFNE or similar, and agree to share info with HCPs).
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