Hi Everyone,
I’ve been thinking about writing this for a while, and I hope you don’t mind that I am using the forum and this message as a kind of therapy. I just feel the need to write down my experiences and thoughts as the partner of a recently diagnosed T2.
Although it is my partner that is coping with the diagnosis and having to deal with the new regime of diet and exercise, I am also affected by the diagnosis and I’ve got to admit that it is tiring, hard work and emotional.
However, things do seem to be going well. I’m hoping for a good improvement when he gets his first post diagnosis HbA1c test, which should hopefully be sometime in October. Although I keep telling myself that this is a marathon and not a sprint and if the improvement is not as good as we are hoping that any improvement is a good thing. The thing is, until we get this result we don’t know if what we are doing is enough, or if we need to adapt even more. I am constantly thinking about this next test result. It’s driving me to distraction! One moment, I am confident the result will be much improved, but then I think what if I am setting myself up for disappointment. I don’t mention this to my OH as he has enough to deal with without my anxieties as well. I have to keep telling myself it will be what it will be, and we can only deal with the result once we get it.
Over the last three months I have learned things I never expected to know about. Although my partner is T2, I have been reading the forum avidly and I have learned so much about the different types of diabetes and I have so much respect for the many members that share their wealth of knowledge and experience. I hope you all know how much it is appreciated.
I am the main cook in the house and I feel a massive responsibility to make sure I am buying and cooking appropriate meals. Again, the forum has been a massive help with this. I have lost all enthusiasm for eating out though, it just seems too stressful to be honest. I am hoping as we continue our journey that we will learn to enjoy going out for meals again.
One thing I have found quite unbelievable is the inconsistency in care and treatment regimes. I would have thought that there would be set guidelines to follow. For example: if your HbA1C is between certain limits then a designated course of action would be taken, but that does not seem to be the case. The treatment plans that people are put on seem varied and I find this quite strange.
Finally (sorry I’m nearly finished rambling now), I know something along these lines was mentioned in a post recently, but I want to mention it as well. Most people mean well, and most people don’t know much about diabetes so I can’t really blame them, but some conversations we have had with family and friends are hard work. You get the ‘so and so eats what they want, and they are diabetic’ or the ‘when can he come off his medication, surely it’s worked by now’ or the ‘he can have a treat, go on, one beer won’t hurt’. And I know everyone means well but when we are still coming to terms with this too it is hard having to hear about everyone else’s opinions on the situation. I find the best way to explain it to people is that my OH now has an intolerance to carbs and that in the same way that they wouldn’t give someone with a lactose intolerance a glass of milk, it’s not really appropriate to offer carby food and drinks to my OH. Explaining things this way does seem to work better.
Anyway, I hope my ramblings make sense. Sorry for offloading on you all (assuming anyone actually got to the bottom of the post) but I just needed to get some things off my chest. It is quite cathartic just writing down my feelings. Mainly I just wanted to say thank you to this forum for giving me so much knowledge and courage to help my OH with his new lifestyle. Thank you x
I’ve been thinking about writing this for a while, and I hope you don’t mind that I am using the forum and this message as a kind of therapy. I just feel the need to write down my experiences and thoughts as the partner of a recently diagnosed T2.
Although it is my partner that is coping with the diagnosis and having to deal with the new regime of diet and exercise, I am also affected by the diagnosis and I’ve got to admit that it is tiring, hard work and emotional.
However, things do seem to be going well. I’m hoping for a good improvement when he gets his first post diagnosis HbA1c test, which should hopefully be sometime in October. Although I keep telling myself that this is a marathon and not a sprint and if the improvement is not as good as we are hoping that any improvement is a good thing. The thing is, until we get this result we don’t know if what we are doing is enough, or if we need to adapt even more. I am constantly thinking about this next test result. It’s driving me to distraction! One moment, I am confident the result will be much improved, but then I think what if I am setting myself up for disappointment. I don’t mention this to my OH as he has enough to deal with without my anxieties as well. I have to keep telling myself it will be what it will be, and we can only deal with the result once we get it.
Over the last three months I have learned things I never expected to know about. Although my partner is T2, I have been reading the forum avidly and I have learned so much about the different types of diabetes and I have so much respect for the many members that share their wealth of knowledge and experience. I hope you all know how much it is appreciated.
I am the main cook in the house and I feel a massive responsibility to make sure I am buying and cooking appropriate meals. Again, the forum has been a massive help with this. I have lost all enthusiasm for eating out though, it just seems too stressful to be honest. I am hoping as we continue our journey that we will learn to enjoy going out for meals again.
One thing I have found quite unbelievable is the inconsistency in care and treatment regimes. I would have thought that there would be set guidelines to follow. For example: if your HbA1C is between certain limits then a designated course of action would be taken, but that does not seem to be the case. The treatment plans that people are put on seem varied and I find this quite strange.
Finally (sorry I’m nearly finished rambling now), I know something along these lines was mentioned in a post recently, but I want to mention it as well. Most people mean well, and most people don’t know much about diabetes so I can’t really blame them, but some conversations we have had with family and friends are hard work. You get the ‘so and so eats what they want, and they are diabetic’ or the ‘when can he come off his medication, surely it’s worked by now’ or the ‘he can have a treat, go on, one beer won’t hurt’. And I know everyone means well but when we are still coming to terms with this too it is hard having to hear about everyone else’s opinions on the situation. I find the best way to explain it to people is that my OH now has an intolerance to carbs and that in the same way that they wouldn’t give someone with a lactose intolerance a glass of milk, it’s not really appropriate to offer carby food and drinks to my OH. Explaining things this way does seem to work better.
Anyway, I hope my ramblings make sense. Sorry for offloading on you all (assuming anyone actually got to the bottom of the post) but I just needed to get some things off my chest. It is quite cathartic just writing down my feelings. Mainly I just wanted to say thank you to this forum for giving me so much knowledge and courage to help my OH with his new lifestyle. Thank you x