Natasha23184
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ThanksHi @Natasha23184 I'm tagging @catapillar as I believe she has a funded CGM due to lacking hypo symptoms. And I think @donnellysdogs might have some helpful input on the question too.
Thanks for your reply. I'm not interested in the Libre for the exact reason you mention. Even though this is purportedly available on the NHS, my area hasn't funded anyone even for this!Don't use CGM but what I understand is your NHS will fund the Abbot Libre device sometimes, but it doesn't alert you when you're low, which is why I always thought it was inferior to the Dexcom which does alert you (and others, like a kid's parent at night). The Dexcom's the only one available in the US until very recently. Reading threads here it's way better overall than the Libre, but probably costs a bit more.
Just wanted to add, there was no obvious cause for this hypo - had been out for a meal and blood sugar rose a little and was corrected via the pump but was fine before I went to bedi.
Hi Natasha, I have a DEXCOM cgm that was funded through Medicare in the US. It is the only one here that is funded. That has to do with the fact that you can make treatment decisions with it. It is surprising to me of how accurate it is. You have to calibrate it 2 times a day. Today my readings have been no larger than 5 points away. It is very correct on which way my blood sugar is headed. I don't have to go low to be able to treat it. When it alarms, I know what to do to prevent it. I did have a low a week ago, due to me giving a bolus that was way out. (Holiday foods) I made the mistake of ignoring the alarms. I was in a very public place and didn't want to draw the attention toward me. I could have excused myself and gone to rhe rest room, but I had just come out of there. It was at a family celebration and my daughter in law would have followed me into her bathroom. I really didn't want a confrontation with her. I talked her father into getting a pump many years ago. He admits he would not be alive today without it. She hates that the pump gave him control back away from leaning on her. Oh well, a lesson learned! He is much healthier today. Her mother is now involved and they even eat healthier now. I have been type 1 for 35 years and have been on a pump for 35 years. I found about a pump right after my diagnosis and went on a pump then. It took changing from one endocrinologist to another, but was well worth it. The endocrinologist I have now suggested my cgm as soon as Medicare started approving them. It has been a really good decision for me. My only advise is go to all the websites and read about all of them. Let the companies that contact you know that you are not ready to place an order but would like all the info. Make the decision that is best for you. You may want to contact your insurance to see which cgm they cover the most and why. That decision was made easy for me as I wanted a cgm that would do the most for me. I have secondary insurance that paid the 20 percent that I would be responsible for. These things are expensive and the supplies that you need each month aren't cheap, either. Good luck getting whichever one you decide is best for you!!
putNo I think you are right - I don't meet the NICE guidelines. Thanks for replying
Hi Sandra, the UK is rather different to the US - this is what you need to qualify for CGM here:put
Let your doctor know and see what he can provide as far as insurance payment. Does he download your meter or pump at your visits to him? I do not know the timeline,as far as the lows go, or how severe they have to be. I was very steady at checking my blood sugars and was told that if you check 4 or more times in 24 hours you qualified for a cgm. I do not know if both requirements have to be met, but my doctor wrote in her notes that I checked more than that. Your doctor will know how to qualify you for one. If you don't qualify for one today, he can tell you how to qualify in the next few months. I had the "1 bad low" also. Now, I really don't know how I did it without a cgm.
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