Thank you for your response. I just feel like I can't keep my numbers steady, I eat the same meals everyday and most of the time I end up in range and other times it'll send me sky high for no reason then I'll be struggling to get it back down. I have also been having another problem where I'll have horrible hypos before I go to bed that's pretty scary and it messes me up for days it's so frustrating. I have actually done some research on this forum and have been seeing post about lantus lows, this really sounds like what is happening to me. My hypos seem to happen about 30 mins after taking my lantus and it happens for no reason whatsoever. I now just want to get my numbers under control so thinking is a pump the best option for me.Hi @Dean_F Welcome to the forum
Out of interest when you say up and down all the time, are you experiencing lots of hypers/hypos ? What does this look like on a daily basis ? Getting access to a pump means meeting the criteria set by your diabetes team, so your starting point is having a chat with your DSN to find out how you can access pump funding, I appreciate that from the outset pumps can look like a magic wand, however they do require alot of work to get ratios set up and bed in and many become disillusioned with them as they don't produce the results to start with, however with alot of effort they can make a massive difference to control and insulin management.
Thank you for your response, this really helpsHello and welcome to the forum!
I've switched from mdi (multiple daily jabs) to pump and wouldn't go back.
In your situation I'd make a list of pros and cons e.g.
Pros -
CONS:
- you will have humalog in small amounts on an houly basis which allows you to tweak those for exercise/illness/busy day at college or a time like dawn when your glucose rises too much.
- Bolus can often be calculated by the pump using your carb/insulin ratio (you have to be good at carb counting).
- Lack of big doses in one go e.g. the lantus dose for me personally means less lumpy bits...
Getting used to the tech then having to order it as well as your usual diabetic kit
You are attached to a pump 24/7 and that sometimes bothers people who don't want to be reminded of their condition.
You will need to persuade your consultant that this will help you i.e. jump through hoops to get it from the NHS since it is more expensive than MDI and not everyone can show an improvement in their HBA1c though most pumpers I know locally find their blood sugars are a lot smoother.
I got mine because I did a lot of exercise and a pump makes that easier. Others have bad hypos or their control has gotten really bad despite their best efforts.
It isn't a magic solution but definitely worth discussing. Gong forward I think lots of diabetics will end up on pumps that talk to their cgms or flash glucose monitors.
Thank you this really helps me. I'll talk to my teamI changed from injections to pumping about 6 years ago and would push back if someone tried to take my pump away from me. However, it has not been easy and it has not reduced my HBA1C by very much.
What it has allowed is much less rollercoastering - highs followed by lows followed by highs followed by ...
This is due to the possibility of smaller doses and varying my basal especially when I exercise.
I had to learn as much about diabetes management as I already knew and I have to be more precise with my carb counting.
Regarding having something attached to me at all times, I have two different experiences. My first pump was a tuby one. I loved the control it gave me but I hated that my diabetes was always on display, I hated that I was always lying on it in bed, I hated that I had to move it every time I sat down or did I different exercise at the gym. My current pump is tubeless. It is smaller (and getting even smaller later this month) so much more discrete, I have found sites that keep it out of the way and love being able to manage it remotely. That said, there are sometimes problems with it being in the same place for 3 days (I have to think ahead about what I will be wearing or doing when I change it), as a larger area is in contact with my flesh, I have less options for sites and I cannot temporarily remove it. So definitely looking forward to the smaller one which will help with some of these issues.
Different CCGs have different approaches, criteria and pump choices. So, if you are interested, the first thing to do is to talk to your diabetes team to find out if they think you are a candidate, how long it will take to get one and what pumps are available.
A simpler option maybe to change your basal insulin. Lantus seems to be an older long acting insulin and there are newer flatter insulins such as Tresiba that many have adopted.I have actually done some research on this forum and have been seeing post about lantus lows, this really sounds like what is happening to me. My hypos seem to happen about 30 mins after taking my lantus and it happens for no reason whatsoever. I now just want to get my numbers under control so thinking is a pump the best option for me.
I was just wondering what you meant by "more precise with my carb counting"? What weren't you doing that you then had to?I changed from injections to pumping about 6 years ago and would push back if someone tried to take my pump away from me. However, it has not been easy and it has not reduced my HBA1C by very much.
What it has allowed is much less rollercoastering - highs followed by lows followed by highs followed by ...
This is due to the possibility of smaller doses and varying my basal especially when I exercise.
I had to learn as much about diabetes management as I already knew and I have to be more precise with my carb counting.
Regarding having something attached to me at all times, I have two different experiences. My first pump was a tuby one. I loved the control it gave me but I hated that my diabetes was always on display, I hated that I was always lying on it in bed, I hated that I had to move it every time I sat down or did I different exercise at the gym. My current pump is tubeless. It is smaller (and getting even smaller later this month) so much more discrete, I have found sites that keep it out of the way and love being able to manage it remotely. That said, there are sometimes problems with it being in the same place for 3 days (I have to think ahead about what I will be wearing or doing when I change it), as a larger area is in contact with my flesh, I have less options for sites and I cannot temporarily remove it. So definitely looking forward to the smaller one which will help with some of these issues.
Different CCGs have different approaches, criteria and pump choices. So, if you are interested, the first thing to do is to talk to your diabetes team to find out if they think you are a candidate, how long it will take to get one and what pumps are available.
There are two reasons why you need to be more precise...I was just wondering what you meant by "more precise with my carb counting"? What weren't you doing that you then had to?
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