sparklesoc
Member
- Messages
- 6
- Type of diabetes
- Type 1
Accuracy wise it isn't the best
If you are not finger pricking, how do you know Libre is accurate?I have not had to test once as I find the Libre very reliable.
I've just posted this on another thread, but desperate for some insights. I'm a first time poster here (or I was a few minutes ago)
My son is 6 years old, diagnosed T1 in November 2018, and has been using the FS Libre for nearly 3 months now. Up to now they have generally been fine. On Thursday we changed the sensor 3 times, and the readings were 2-3 mml different to the blood prick readings. On the first one, we put it into the side of his arm and not the back. I read somewhere that if it goes into a muscle it will be inaccurate. So we changed it. The second one, there was a bleed when we applied the sensor, so we thought it was because of that. So we put a third one on, another bleed and again a difference of 2 to the blood test. We called Abbott and they suggested waiting 24-48 hours, after a bleed. So we are waiting, while in the meantime, can’t send him to school and expect teachers to do blood tests instead using a simple scanner. (Before anyone calls social services - He does have a careplan, and we and school keep to it rigidly, but we rely on the libre to make it work. DS's teachers are trained in doing blood checks but we don't want to drive him mad.)
Have any of you ever had this experience? Firstly, how common is it to bleed when applying the sensor? Secondly, does a bleed affect the accuracy of the sensor? And, if bleeding does not affect it, we had three different sensors giving wild results!!
The thing that is confusing us here, is that we've used probably 5 or 6 sensors to date, and they've all been fine. Now suddenly, we have 3 that are faulty?! For us, we don't want to finger prick a 6 year old constantly, the libre has been a lifesaver, but now we feel we are driving on a dark road without any lights, as we are giving food and don't know for certain where his levels are.
I have had the Medtronic 640g pump for a year now which I have found fantastic! I was at my Diabetic appointment a few weeks ago & I have been encouraged to go on the Libre Sensor. What do users with a pump think of the Libre sensor?
Our trust only gives patients with persistent hypos/poor hypo awareness the 670g pump with CGM sensor.
Is the Libre Sensor useful even though it doesn’t communicate to the pump? Many thanks
Hi Helensaramay. I've been T1D for 50 years and still have very good awareness signs of falling or rising BS. I know that the sensor readings tend to lag a finger prick by 10 mins or so (in my case) but, the arrow trend indicator is very useful in confirming what I believe is happening. My son-in-laws niece is also on the Libre and she thinks its fantastic. Perhaps its not for everyone.If you are not finger pricking, how do you know Libre is accurate?
I find the graphs and trends amazing but the numbers are not accurate. For example, Libre has read -0.7 when I was completely articulate.
Hi Helensaramay. I've been T1D for 50 years and still have very good awareness signs of falling or rising BS. I know that the sensor readings tend to lag a finger prick by 10 mins or so (in my case) but, the arrow trend indicator is very useful in confirming what I believe is happening. My son-in-laws niece is also on the Libre and she thinks its fantastic. Perhaps its not for everyone.
I just checked my BS. Sensor showed 7.0 but, meter revealed that my BS is 9.3 (2 hours after B/fast). I didn't realise that the difference in accuracy was so large. Well, I guess it's back to checking my BS by finger pricking at injection times.
Hi, I have been using libre sensor for 18months now and find that you can’t just put one in and use it straight away, my libre runs out on a Saturday morning so during the Friday I put my new one in and let it settle for 12/18 hours before I activate it, it’s almost like it has to absorb the fluid for a while before it can adjust. Having done this my readings when activated the following day on the new sensor are spot on to those I took on my dieing sensor.I've just posted this on another thread, but desperate for some insights. I'm a first time poster here (or I was a few minutes ago)
My son is 6 years old, diagnosed T1 in November 2018, and has been using the FS Libre for nearly 3 months now. Up to now they have generally been fine. On Thursday we changed the sensor 3 times, and the readings were 2-3 mml different to the blood prick readings. On the first one, we put it into the side of his arm and not the back. I read somewhere that if it goes into a muscle it will be inaccurate. So we changed it. The second one, there was a bleed when we applied the sensor, so we thought it was because of that. So we put a third one on, another bleed and again a difference of 2 to the blood test. We called Abbott and they suggested waiting 24-48 hours, after a bleed. So we are waiting, while in the meantime, can’t send him to school and expect teachers to do blood tests instead using a simple scanner. (Before anyone calls social services - He does have a careplan, and we and school keep to it rigidly, but we rely on the libre to make it work. DS's teachers are trained in doing blood checks but we don't want to drive him mad.)
Have any of you ever had this experience? Firstly, how common is it to bleed when applying the sensor? Secondly, does a bleed affect the accuracy of the sensor? And, if bleeding does not affect it, we had three different sensors giving wild results!!
The thing that is confusing us here, is that we've used probably 5 or 6 sensors to date, and they've all been fine. Now suddenly, we have 3 that are faulty?! For us, we don't want to finger prick a 6 year old constantly, the libre has been a lifesaver, but now we feel we are driving on a dark road without any lights, as we are giving food and don't know for certain where his levels are.
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