I am a T1 diagnosed 30+ years ago and now on a Medtronic 670G pump. No fun to deal with this on a 24x7 basis. My family really doesn't understand what this is really like. My wife doesn't understand but does visit me in the hospital when that part happens. On the other hand, this is not cancer, or MS or ALS or or or. It is a reasonably manageable disease and may contribute to a longer life than otherwise as I am constantly worried about what I eat, when I eat, exercise, and see my doc regularly. So there's some good news.Hi There
I am hoping that the fabulous community here will post replies on this thread about the subject in the title.
or possibly provide links to people's blogs on the subject , or even copy a link to an old topic that covers this area
this topic could then hopefully be something that could be shown to gather support from family members, it could be helpful to newly diagnosed families as well as families with a D peep going through issues at the present time.
thanks so much for reading and for posting if you are able.
all the best !!
I've non diabetic friends who often show 9s,10s and 11s particularly after meals.
Currently, life as a type 1 for me is scanning my arm with my Libre every half hour or so and taking a series of small injections (typically around 10 a day at present) through the day.
Injections and Libre scanning is the relatively easy part.
Needing to sometimes wait to eat until your sugar comes down so that you don't spike your sugar levels super-high from an already high level is one of the annoyances.
Having to make dozens of not easy decisions about how much to inject and when, what to eat, how and when. Taking into account a range of different factors every single can be mentally tiring some days.
Never being able to go much more than 500-yards without taking kit and glucose with you just in case your levels start dropping (or sometimes rising -depending how far you're going).
Having your emotions and ability to cope (physically and mentally) tied to your sugar levels. Low sugar levels making you slow and unable to cope with usual tasks that would be a doddle. High sugar levels making you irritable and/or lethargic plus can also initiate short term depressive symptoms. Both low and high sugar levels amplify emotions making it that bit harder to keep one's head together under some situations.
Having to delay or interrupt sex because of low blood sugar.
Urinary tract infections being more likely if sugar levels have been high for several hours or over a number of days -particularly if stressed at the same time.
Occasionally having to battle off feeling depressed about the risk of developing long-term complications if sugar levels having been high for longer than I'd like.
Mostly for me, type 1 diabetes is fine to deal with when control is good. But, when control goes a bit skewiff, the little persistent things can add up to the short term difficulties and that's when things get tough and you want to scream a bit inside or out.
Type 1 can amplify things. When life is tough, the type 1 makes everything that bit harder. However, perhaps the dealing with the tough stuff makes us a bit sunnier and brighter when the good times do happen?
Ed
That could be quite depressing for a newly diagnosed type 1 to watch , just take it from someone who's been doing this for 47 years it has never ever been anywhere near that bad !If you go to YouTube and type in #Type1uncut you will find some useful and informative video's of what it's like to live with type 1 diabetes, here's some information about how #Type1uncut came about:
https://www.diabetes.org.uk/Guide-to-diabetes/Type-1-Uncut-for-young-adults/
I quite like the following, it's an amusing take on the frustrations of everyday life with type 1 like testing, injecting and clinic appointments to name a few:
Currently, life as a type 1 for me is scanning my arm with my Libre every half hour or so and taking a series of small injections (typically around 10 a day at present) through the day.
Injections and Libre scanning is the relatively easy part.
Needing to sometimes wait to eat until your sugar comes down so that you don't spike your sugar levels super-high from an already high level is one of the annoyances.
Having to make dozens of not easy decisions about how much to inject and when, what to eat, how and when. Taking into account a range of different factors every single can be mentally tiring some days.
Never being able to go much more than 500-yards without taking kit and glucose with you just in case your levels start dropping (or sometimes rising -depending how far you're going).
Having your emotions and ability to cope (physically and mentally) tied to your sugar levels. Low sugar levels making you slow and unable to cope with usual tasks that would be a doddle. High sugar levels making you irritable and/or lethargic plus can also initiate short term depressive symptoms. Both low and high sugar levels amplify emotions making it that bit harder to keep one's head together under some situations.
Having to delay or interrupt sex because of low blood sugar.
Urinary tract infections being more likely if sugar levels have been high for several hours or over a number of days -particularly if stressed at the same time.
Occasionally having to battle off feeling depressed about the risk of developing long-term complications if sugar levels having been high for longer than I'd like.
Mostly for me, type 1 diabetes is fine to deal with when control is good. But, when control goes a bit skewiff, the little persistent things can add up to the short term difficulties and that's when things get tough and you want to scream a bit inside or out.
Type 1 can amplify things. When life is tough, the type 1 makes everything that bit harder. However, perhaps the dealing with the tough stuff makes us a bit sunnier and brighter when the good times do happen?
Ed
Can I recommend a DAFNE (Dosage Adjustment For Normal Eating) course to everyone who is a Type 1. It's a 5 day course (or was when I did it 15 years ago) and a bit like a Freestyle blood sensor, is life changing. It was available via my diabetic consultant at his venue in Tunbridge Wells. It was an intensive week but oh sooo useful in gaining the knowledge to manage/balance food/insulin intake. And that's what it's about isn't it?? I've now been type 1 for 51 years and so when I took the course, very cynically I confess, after about 36 years at that time, and considered my knowledge to be good enough to effectively manage my diabetes, I discovered a whole new way of getting it right. Like many others I'm sure, I've suffered with this chronic condition long enough for it to become a real daily nuisance even now There's no end to worrying about the condition 24 hours a day if you want to remain in good health and without the worries of the dreaded complications that might interfere with your life e.g. circulation problems, loss of vision, kidney issues and of course the possible loss of a limb. It's all of these potential problems that have driven me to look after myself as best I can and quite successfully. And DAFNE will seriously help with this and give you the confidence you need to make better choices and literally allow you to eat anything and I do mean anything. Will you be able to eat a banoffee pie and custard, a spotted **** and treacle, a baked alaska.....yes it will.....but not all of them in one evening!! Would you have done so if you hadn't been a type !? (you might have...piggy). But honestly, find out if a course is available near you , hopefully funded by your consultant or GP. The costing is minimal compared with the NHS costs of dealing with the complications of bad control. Good luck to you all.Hi There
I am hoping that the fabulous community here will post replies on this thread about the subject in the title.
or possibly provide links to people's blogs on the subject , or even copy a link to an old topic that covers this area
this topic could then hopefully be something that could be shown to gather support from family members, it could be helpful to newly diagnosed families as well as families with a D peep going through issues at the present time.
thanks so much for reading and for posting if you are able.
all the best !!
I'd agree with this all the way. DAFNE was the first step I'd taken in years (been T1 for 40+ years now), this led to me going on a pump and from there I've been using the MiniMed 780 along with the guardian sensor for the last 18 months. Total transformation for me. HBA1C is the best it's been for as long as I can remember.Can I recommend a DAFNE (Dosage Adjustment For Normal Eating) course to everyone who is a Type 1. It's a 5 day course (or was when I did it 15 years ago) and a bit like a Freestyle blood sensor, is life changing. It was available via my diabetic consultant at his venue in Tunbridge Wells. It was an intensive week but oh sooo useful in gaining the knowledge to manage/balance food/insulin intake. And that's what it's about isn't it?? I've now been type 1 for 51 years and so when I took the course, very cynically I confess, after about 36 years at that time, and considered my knowledge to be good enough to effectively manage my diabetes, I discovered a whole new way of getting it right. Like many others I'm sure, I've suffered with this chronic condition long enough for it to become a real daily nuisance even now There's no end to worrying about the condition 24 hours a day if you want to remain in good health and without the worries of the dreaded complications that might interfere with your life e.g. circulation problems, loss of vision, kidney issues and of course the possible loss of a limb. It's all of these potential problems that have driven me to look after myself as best I can and quite successfully. And DAFNE will seriously help with this and give you the confidence you need to make better choices and literally allow you to eat anything and I do mean anything. Will you be able to eat a banoffee pie and custard, a spotted **** and treacle, a baked alaska.....yes it will.....but not all of them in one evening!! Would you have done so if you hadn't been a type !? (you might have...piggy). But honestly, find out if a course is available near you , hopefully funded by your consultant or GP. The costing is minimal compared with the NHS costs of dealing with the complications of bad control. Good luck to you all.
After being T1 for 59 years, I still get bogged down with it tbh. I got to a state where I thought, I've got Diabetes I'm stuck with it for life but I'm ruling it not the other way roundHi There
I am hoping that the fabulous community here will post replies on this thread about the subject in the title.
or possibly provide links to people's blogs on the subject , or even copy a link to an old topic that covers this area
this topic could then hopefully be something that could be shown to gather support from family members, it could be helpful to newly diagnosed families as well as families with a D peep going through issues at the present time.
thanks so much for reading and for posting if you are able.
all the best !!
as for access to libre here is the latest NICE recommendations which clearly say that all type 1 diabetics should have access to this technology.Johncon , you said you were dragged kicking and screaming to go on a pump ,in my 47 yr experience of type 1 I would say it would be the other way round for me and I would have to drag them to get a pump , not that I want one and am in the proverbial rut with my daily pen injections and blood tests , I did ask about a Libre this year but was told no chance , it does still seem to be a postcode lottery as to the treatment we get .
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