A lot of hospitals don't seem to like funding Omnipod, not sure if it is because it's more expensive than the others my hospital doesn't provide the omnipod as an option either. In terms of is it worth it, it's all down to personal preference, for me it was worth it and still is. It helped my dawn phenomenon massively and now I'm on hybrid closed loop its even better. My HbA1c hovers around 49 or below for the most part with over 70% time in rangeCould I ask those of you who have pumps - are they worth it? Someone from my clinic seemed to imply that they aren't. I'm just wondering whether to go to all the expense of privately funding.
Was your HbA1c higher in order for you to be prescribed a pump or are you in a part of the country where it's easier?A lot of hospitals don't seem to like funding Omnipod, not sure if it is because it's more expensive than the others my hospital doesn't provide the omnipod as an option either. In terms of is it worth it, it's all down to personal preference, for me it was worth it and still is. It helped my dawn phenomenon massively and now I'm on hybrid closed loop its even better. My HbA1c hovers around 49 or below for the most part with over 70% time in range
I am wondering if I have misunderstood, but I am curious. If your hospital does not provide the Omnipod, how did you acquire your Omnipod?A lot of hospitals don't seem to like funding Omnipod ...... my hospital doesn't provide the omnipod as an option either....... for me it was worth it and still is.
I got mine about 10 years ago now, I fit the NICE guidelines at the time. My HbA1c was probably raised but essentially I had dawn phenomenon and I couldn't change my basal insulin to twice daily as giving it at night gave me hypo's overnight that I never woke up toWas your HbA1c higher in order for you to be prescribed a pump or are you in a part of the country where it's easier?
I'm on the Medtronic 780gI am wondering if I have misunderstood, but I am curious. If your hospital does not provide the Omnipod, how did you acquire your Omnipod?
I was wondering whether anyone had any advice on this question? I had my appointment with the consultant this week. Still no pump, but he did agree to putting me on the waiting list, which is something I suppose, though he said it would be at least three years. He also said that he would write the necessary letter if I decided to fund privately, but sort of implied that doing this wouldn't be worth it, other than freeing up some headspace. He said that it was a postcode lottery, in that some ICBs just go for it. My dilemma is whether I should stick it out or fund privately. Any comments from those of you with pumps?Could I ask those of you who have pumps - are they worth it? Someone from my clinic seemed to imply that they aren't. I'm just wondering whether to go to all the expense of privately funding.
If you are looking into privately funding an insulin pump, please also ask for the price of infusion sets (unless you choose a tubeless pump).I was wondering whether anyone had any advice on this question? I had my appointment with the consultant this week. Still no pump, but he did agree to putting me on the waiting list, which is something I suppose, though he said it would be at least three years. He also said that he would write the necessary letter if I decided to fund privately, but sort of implied that doing this wouldn't be worth it, other than freeing up some headspace. He said that it was a postcode lottery, in that some ICBs just go for it. My dilemma is whether I should stick it out or fund privately. Any comments from those of you with pumps?
I once heard a former UK Secretary of State for Health (who was a qualified doctor) say that healthcare in the United Kingdom has always been rationed.Thank you very much for this. I've read some of the earlier posts about advantages and disadvantages. But what I find really annoying is the postcode lottery element, when some (a lot) of us are denied even the chance to try a pump, in my case after nearly 43 years of injections. Just basing the decision on predicted HbA1 is so one dimensional and short sighted. I'm wondering if there's some way of getting a petition going, or similar, to expose those responsible for making these decisions.
I was (still am) a big admirer of Ms Lucas. However, I understand one of the reasons she decided to stand down as an MP at the last election, was her frustration at being unable to influence HM government policy enough - particularly on climate change - without being part of the actual government.Thank you. Very interesting and very dispiriting, although do you think this might provide a ray of hope?
I understand that even current NHS England's diabetes technology lead, who was instrumental in getting NICE TA943implemented, would like the current rather strict hybrid closed loop eligibility criteria relaxed. My understanding is that clinical trials/studies are happening in the background to achieve that.
I have written to my MP, who was sympathetic, but not much more, I intend to write to her again and ask if this could be raised more generally. I feel sure that her predecessor, Caroline Lucas, would have been more proactive. I have also looked into changing clinics, but the trouble is, other localish ones are bound by the same ICB rules. I suppose it would be fairly easy to persuade a consultant that one was planning to get pregnant - but unfortunately not at 68! It seems we're stuck.
Hi, does anyone have a view on this, please? Also, I got into a discussion with a well known diabetes medic on Instagram. He was lauding the success rate of providing pumps to younger patients and I suggested that whilst this was great, those of us who have been T1 for decades seemed to be getting lost in this, and that basing decisions solely on predicted HBA1C results seemed somewhat one dimensional in that we might well have other issues affecting our physical and mental health. His response was to ask who he should not be providing this to in order to prescribe to older adults, which missed my point somewhat and was not, in my view, a question that I should be expected to answer as a patient. So I'm getting absolutely nowhere, other than that my consultant agreed to put me on a waiting list (by which time, if I ever get one, I will be in my 70s and will have been injecting for around 46 years). Oh I don't know, it's all so dispiriting. Do you think there's ANYTHING more that could be done as a group of patients? And again I ask, are pumps worth all this? Thanks for reading and have a good day all.Could I ask those of you who have pumps - are they worth it? Someone from my clinic seemed to imply that they aren't. I'm just wondering whether to go to all the expense of privately funding.
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