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CGM update

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This thread is now closed. Please contact Anna DUK, Ieva DUK or everydayupsanddowns if you would like it re-opened.
AJLang

AJLang

Well-Known Member
Relationship to Diabetes
Type 1
Just wanted to say that the CGM is still helping me loads. Although my BGs aren't perfect because of the gastroparesis there has been a massive improvement since the arrival of the CGM. A lot fewer high highs and the safety of the CGM alert when my BGs go down. I'm feeling much better than I have in a long while and no longer need to sleep in the afternoons which I was doing before because of the tiredness. I'm so happy because of the CGM.:D and feeling nearly normal again
 
I am soooo pleased to hear this Amanda 🙂 Hurrah for the CGM! Your diabetes management is difficult enough with the gastroparesis, so it's great that you have found something that eases that and moreover has given you more energy and a better quality of life. It's a shame that you have to pay for it, I really think that for someone with your problems, and with such clear benefits, it should be funded by the NHS. 🙂
 
I couldn't agree with you more Alan about NHS funding. I've had to borrow the money to pay for the CGM and by the time I've managed to pay it off it will be time to buy the replacement receiver/transmitter (they last approximately 12 months).
 
It sounds like you have a good case to push your consultant with for funding, given the improvements and potential savings, plus it's cheaper than a pump (which I think you should also get!) 🙂
 
Status
This thread is now closed. Please contact Anna DUK, Ieva DUK or everydayupsanddowns if you would like it re-opened.
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