I'm in St Albans and we don't have it either. My GP said from April it won't be postcode lottery so I should get them on prescription. Chemist looked at me like I was mad! Emm no St Albans is a fluent area so you miss out!No funding for Freestyle libre in Suffolk apparently last area in country to get funding so no choice but to pay for yourself despite situation! Frustrated by this as weight gain due to managing hypos hypers eating much less than I used to but no one able to help. I do exercise daily too. Had diabetes since 4 years of age now 57 years. Like you when young had no warnings but developed more awareness as young adult hopefully you will too, good luck hope it gets easier for you.
Good luck .Just checked it definitely says no longer postcode. Depends on the need?
MIght show to my chemist
Hi all,
I'm a type 1 (newly diagnosed) and Got my 6 month check up (it's actually about 9 months now.. earliest they could get me in!) tomorrow.
I have had more or less NO education apart from one dietician appointment a week after diagnosis so have been pretty much in the dark this whole time and playing a guessing game..
I am self-funding a cgm (Dexcom) and it has definitely saved my life - I have no hypo awareness 99% of the time.
I am reliant on my Dexcom but obviously it is very expensive and not something I want to be paying £160 a month for in the future - do clinics provide funding/assistance for cgms is my main question?
I feel really neglected by my clinic and that because I'm 22 I'm in a bit of limbo - not cared for by the adolescents team and also not being cared for by the adult team... Just very worried about the long term issues that my highs can cause - average sugar is usually around 8/9 - not great!!
Thank you in advance
In regards to hypo awareness, this can usually be regained if you manage the levels well for a couple of weeks (minimize time in hypo) the body adjusts pretty quick.
That's awful I'm so sorry it's being taken away from you! I hope they manage to sort it out soonI got the freestyle libre on a trial over month ago and fit the criteria of at least 8 times a day testing my levels, and have to say that in the 8 yrs i have had type one diabetes (i am 47 yrs old now) this is the first time i have ever seen / understood my blood sugar levels and the effects of insulin and food. However after been on the system now for 5 weeks i get a phone call from my doctors saying that the locum doctor who saw me, incorrectly issued me with a prescription for the sensor and i had to go to my diabetes centre and they would give me the prescription, i call them and they said its the doctors. now both refuse to issue both and i am losing it now and back to finger pricking when my next sensor has expired.
So frustrating as this is nothing to do with patient care, and only to do with funding, and since i have been struggling for a few months know, this was a small light at the end of the tunnel in trying to get a more settled level.
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