A bit more about me

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Red Pumper

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Relationship to Diabetes
Type 1
Hi, wasn't sure whether to post this here or not as I've already introuced myself, but it seems as good a place as any.
Since I joined the forum, I've read most of the new posts and a few of the older ones and see people going through most of what I've been through over the years. So I thought it may be a good idea to let everyone know a bit more about me in case they recognise anything that I've been through and want to ask me anything. So here goes, I hope it isn't too long:

I was diagnosed and having Type 1 diabetes when I was 9 years old back in 1979. I went into hospital for two or three days while they sorted out my insulin dose and wasn't allowed home until I could inject myself and my parents had also done an injection.
Initially I was on one injection a day which soon moved to two.
I went through my last year at primary school and my time at secondary school really just getting on with it, testing my BG with the old BM sticks and old style lancets (which really hurt). The diabetes never really stopped me from doing anything as a child but I recognise the issues with testing and hypos that Parents have been posting about. My control was generally good but I did have a couple of debilitating hypos at school when the staff didn't really know how to treat it.
I left school and discovered alcohol and nights out. I just carried on with the same routine of two injections a day, testing now and again but nowhere near as often as I should have. Through my late teens and twenties, I neglected control of my diabetes, probably ran my BG too high most of the time. My health didn't seem to suffer (or so I thought) and apart from a couple of hypos at work (where I actually passed out and needed the attendance of an ambulance) the diabetes didn't really cause any problems.
Then I hit my thirties and this is when my bad control through my teens and twenties caught up with me.
The HbA1C test had just been introduced and my first result was above 9. I was called to see the diabetes consultant, was given an insulin pen and moved onto four injections a day, I also had to see the DSN every month or so to try to improve my control. I managed to get my HbA1C down to around 7.5 but no lower.
In around 2003 I had a small bleed in one of my eyes but the opthalmologist couldn't see anything wrong. About a year later I had another, much larger bleed. This time the opthalmologist said that I had developed proliferative retinopathy and they started laser treatment. Over the next three or four years, I had numerous bleeds, some of them quite bad but luckily never in both eyes at the same time. I've had approximately 4000 lasers to each eye to try to control the growth of the new blood vessels. Since the latter half of 2007, I have had no bleeds and things seem to have settled down. To the extent that I now go the see the opthalmologist every six months instead of every three months. I can no longer drive as the laser treatment has affected my field of vision to the extent that I failed the DVLA test, mys vision is also quite poor in low light.
In the meantime I have really struggled to get my diabetes under control. I tried various insulins, including the new Lantus and Levemir, Until very recently I was on five injections per day - four humalog and two lantus.
The last three weeks have been the best three weeks of my diabetes life since my schooldays. I started using an insluin pump on 10 February. I spent three days visting the DSN to set up the pump and check my initial dosage etc. and I've also been back for two further follow up visits.
Although I'm still in the stage of getting the basal and boluses worked out, it has been a brilliant three weeks. I can count the number of BG readings of above 10 on the fingers of one hand and the vast majority of my readings have been in the 4-7 range. I've had to treat quite a few hypos as my basal rate is still a little high but so far it's been great.
I now have lots more energy and I've lost about 6 lbs.

My apologies if I've gone on a bit but thought it may be worth sharing what I've been through in case anyone else is going through the same things and needs to talk.
It's a long time ago now but if any parents out there want to know what it's like from a child's perspective, just give me a shout.

Thanks for reading,

Keith.
 
thank you keith for that , its always interesting to hear other peoples diabetic stories. there are a few youngester/young adults on the forum who im sure can identify with you and get valuable help from your experiences x
 
Keith, thank you for sharing your story. I really hope that the pump brings stability to your diabetes. Do keep us informed.

My son (13) started on a pump last July and it has made such a huge and positive difference. The pump does have its downsides and does need to be managed but, for us, the positives hugely outweigh the negatives.

Mand 🙂
 
Hi Mand,
my experience with the pump has all been positive so far. I thought being attached to it 24 hrs a day would be a problem but I'm amazed how quikcly I've got used to it.
I'm sure there are more downsides for children than there are for adults.
My Diabetes Nurse is absolutely fantastic, her knowledge is second to none and the level of support is I get is brilliant. They should all be like that.
 
Hi Keith,
Thanks for posting your story. My son is 11 and these are the things i worry about most - teenage rebellion etc. He has been on a pump for 6 months now and hba1c gone down from 9.6 to 7.1 - so very pleased with that. It sounds like you are now on top of things and its great that you are willing to share your experiences as i think it will help so many who may not be taking things as seriously as they should.🙂Bev
 
Hi Keith,

I read all of that properly- I am pleased with myself! 🙂

Its really nice to read someones story, because no two people have had any experience the same with diagnosis and diabetes as a whole. Do you know until I read what you had wrote I hadnt even considered that there was at some stage no hba1c test?! Of course it had to be introduced at some time but I thought it had been round ages and ages. That must have been a really strange time for everyone- imagine having this test brough in? I wonder what degree of accuracy it was in the early days as well??

What pump do you use? I have a medtronnic veo. Probably 9-ish months now. Pumping has changed my diabetes so much, how I feel, my motivation, my blood sugars are slowly getting better.....its a massive change. If someone took it away from me tomorrow I dont know how I would cope!

Really nice to read your story Keith.


Louisa x
 
Hi Bev,
I think the pump will help your son keep on top of his diabetes control as he moves through his teens and twenties as a pump requires much more management than injections to guard against things like DKA.
I think the important thing is that you continue to keep an active interest in his diabetes management. As soon as I left school, my parents assumed that I was looking after myself and doing the things that I should have been doing.
The problem with diabetes related complications is that we are told about them but we are also told that seruous complications are relatively rare. This may be the case but I don't think they are common among diabetics who have poor control as I did.

Hi Louisa,
I think i got my first HbA1C test done in the early to mid nineties. For the first few years after my diagnosis, there wasn't any way of home blood testing. We had to test the glucose in our urine, this would give a general but in no way accurate guide to how things were going. There was no way of knowing for definite whether you were having a hypo, you just had to guess from the way you were feeling. How times change.
I'm using a Accu-Chek Spirit pump, it's great so far.
 
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