Hahaha this was the most human response so farI've apologised to my long suffering hubby about being a bore about diabetes but I find explaining things out load actually helps me understand the topic, I know the cut off point is when he lapses into a boredom coma or starts snoring, I suspect though I may as well be talking to myself most of the time bless him he is so patient
Jan
I'm at the other end of the spectrum to you - I'm retired and recently diagnosed type 1. I found that most friends wanted to know about what I can/not eat mainly so that when we eat out, or at each others houses, they don't feel embarrassed by serving something really high in carbs. For everyone else, I don't mention it unless the subject of diet comes up.Thank you for understanding that it's a big deal to me. I think a lot of people just see me test and inject at school once a day and think that that's all there is to it.
I only use the opportunity to educate folk on my Diabetes .
When 'they' ask me anything about it ...
Food , injections, pain/needles/lancets , routine , diagnosis etc .
I do it in a with pride positive manner .
I refuse to feel it should hinder me in any way .
Folk 'listen more' this way I have found .
Everyone has been great about it too .
I think my twitter peeps would agree with you but they either have diabetes, are nurses or frequent Glastonbury festival (other festivals are available but not in remotely the same league!) In real life I don't mention it too often, only a few close friends get my wrath on that front but that could be that I am a nurse and most of my friends are nurses (or other healthcare professionals) and we are notoriously an unsympathetic bunch with each other!Does anyone else feel like they talk about their diabetes a lot of the time? I feel as though I want to explain it and I want everyone to understand it and know that it is difficult to live with. But I also don't want it to define me and moan about it too much. How do you find the right balance?
Yeah it's nice that I can come here and vent! And you guys get what I mean. And sometimes I read something that someone with T1 has written that I have felt but never really put into an actual thought/wordsYes I totally agree. I will normally only discuss my diabetes if it will be beneficial to another diabetic, I don't talk about it too much outside that scenario. Unless someone asks me a question on it and it's not one of those daft ones !
I work with vulnerable adults and I am used as a focal point for anyone who may be diabetic who may need a little guidance so I get good chance again to use my experience in hopefully benefiting some one else.
This forum is great though for giving guidance and also receiving. And we can go on for as long as we like about it !
SAMEtry not to be a bore.
Sometimes I fail.
I understand what you're saying about it being hard for it not to define who you are, I went through the same thing when I was first diagnosed because I was recovering from Diabetes Ketoacidosis and I felt unwell all the time and had to miss a lot of school and I looked unwell, but now I have recovered and have better control over it it's definatley not defining me and things are getting back to normal! Thanks for the commentSometimes when newly diagnosed we want to see what peoples reactions might be, I feel a bit like you do sometimes. As for diabetes defining who you are, it can be difficult for it not to, again especially when you're newly diagnosed as most lose weight and go through huge lifestyle changes, this can spark interest from others.
I expect some of these issues quieten down over time or at least when people and those around you get bored of asking questions, it becomes old news.
I'm sure it's a little different for everyone, those are just my thoughts since being diagnosed in January.
Daks
When I was diagnosed I tended to explain stuff to family & friends, now I rarely talk about it. I start a new job in a couple of months time and I'm contemplating whether to tell them. I don't want to start and be defined as the guy who's got diabetes, so will probably just tell people i work closely with after a few months, or just when it sees a good time.
I don't think I'll do that again. I had a contract a job on a research team at an Irish university. I had been diagnosed three years earlier and was still struggling to get my levels under control. I was very self-conscious about being moody, irritable or anxious and felt it necessary to try and explain this to the people there so that they wouldn't get the wrong idea if they thought I was a bit off. Previous experience had taught me that they would quickly take it as a personal affront if I was 'off' with them.
Didn't matter a damm. They decided I was unpleasant and grumpy and would have nothing to do with me. Two years without anybody speaking to me outside of the monthly meetings of the project team. I had no work to do because nobody would work with me. I have worked hard to get my experience and develop my skills and I do NOT like having no work.
The contract ended six months ago. I really balk at the idea of finding another job and I have had minimal contact with people in that time - and it's bliss.
Thank you for understanding that it's a big deal to me. I think a lot of people just see me test and inject at school once a day and think that that's all there is to it.
We use cookies and similar technologies for the following purposes:
Do you accept cookies and these technologies?
We use cookies and similar technologies for the following purposes:
Do you accept cookies and these technologies?