Umarth, i would respectfully suggest that as a T1 this may be OK for you as you can control your D by means of insulin, but for Diet & Exercise T2's your carb count could be grossly excessive.If you are that worried about the food in hospital when you are in then contact your dietician. I had to go in for two weeks in October last year and I was offered a pass to the public restaurant to top up what I was eating. If you are worried about the high carb count then may I suggest changing to a regime that deals with carb counting? I did and I personally can eat practically anything! Take for example this lunchtime. My lunch consisted of two sandwiches and a large packet of crisps. Total carbs was around 200. My test pre evening meal had my bloods on a mere 8.5........ I am a type 1.
I found the hospital food to be one of the worst things about my stay and recovery from a DKA two years ago.
The undiagnosed nerve damage prevented me from keeping food down and the anti-nausea meds were not too helpful. I was bullied by the catering staff for wasting food or meals were forgotten and the nurses brought me cuppa soups instead!
In ICU all the food tasted very strange and made me sick, I asked my partner to bring in tomatoe soup and was so relieved each day when he arrived and I could get it heated up. I'd always had fruit and yoghurts when ill before, but these were to acidic and off the menu, not that I knew, it took four days of bringing them back up before one of the nurses suggested they might not be suitable.
On the ward after a week I managed to keep some porridge and milk down, so asked for milk to drink. However I couldn't eat it until after the anti nausea had kicked in, the nurses were adamant that I had to wait 9 hours between shots, so after stomach convulsions in the night, planning to have a dose 9 hrs before breakfast was not exactly on my mind. Resulting in me missing the regular breckfast session and annoying the nurses later asking them if the might actually fetch me something to eat. That worked along with the daily soup from my partner. I was not informed I could ask for some or biscuits/crackers (which I sucked) at any time and was ravenous by the time he arrived.
Cauliflower cheese seemed to be the only diabetic option on the menus, which includes flour in the sauce, so not low carb. I regularly ordered the farmhouse soup or some such, but never received it.
Upon discharge the nerve damage remained undiagnosed and I spent two weeks on a liquid diet of soups and milk at home' continuing to take anti-nausea meds.
The ICU care was phenomenal, they saved my life! But the food and general diabetic care was abysmal
Robin redbreast
Thank you for your reply. It has been quite literally hell theses last few months. He was very sick and since the GF diet was started he has improved so much, which I think will help with his ability to say no to GF food when it's offered. My 10 year old daughter has also been very ill. They thought she may have had a brain tumor , with so many scary symptoms, thankfully she dies not. The GP suggested she see the Gastroenterologist as my son had been diagnosed and they confirmed she also has Coeliac disease, then they suggested my husband and I have tests and I was confirmed 3 weeks ago ( endoscopy procedure is awful)!!
We are now eating GF and my daughter is also feeling so much better and I am Losing weight so there is always a silver lining to every cloud.
As for my son, my husband and I tell him he is our hero every day. He copes so well with all that the world has thrown at him and although we all have our bad days , every day is a little better than the last.
I am now humbled by all those who deal with type 1. I just hope that I can be a good enough mother to be able to arm him with all he needs before he goes off to into the big wide world, plus also praying for a cure like everyone else I'm sure.
I am waiting to hear back from diabetes.uk as I would like to meet parents in a similar situation, I do feel very isolated by this, it has certainly showed me who of my "friends" are.
Hope you are well
Lucy
I just gave up and ate whatever muck was served up, trying to leave the carbs to one side. I figured that I would get out of there quicker if they could tick the box for having a healthy appetite. It worked. As long as you can eat, drink, pee, poo, and wash yourself they let you home.I've been in many different wards but never in a diabetic ward. Do they make any attempt to cater properly for diabetics? I've seen the 'D' next to various meals but never took much notice before. Although i seem to remember that all the diabetic desserts were milk puddings!
Reading this article doesn't give me much comfort, the photo is a diabetic nightmare! www.theguardian.com/commentisfree/2015/mar/02/hospital-food-nutrition-recovery-ministers?CMP=fb_gu
I've got a week or two in hospital coming up later this year so am wondering what I can expect? (Not in a diabetic ward, I'll be in colorectal surgical).
And what I should take in with me to ensure I don't starve?
I just gave up and ate whatever muck was served up, trying to leave the carbs to one side. I figured that I would get out of there quicker if they could tick the box for having a healthy appetite. It worked. As long as you can eat, drink, pee, poo, and wash yourself they let you home.
Good luck, and happy birthday @rowan .
Unfortunately I won't sacrifice my health to pander to others little delusions so I don't eat hospital **** to please anyone!
There was no delusion. When I was in hospital last year, the only way anyone was discharged was if they had all the boxes ticked by health care assistant. Eating hospital food was one of them. So I ate.
If you are that worried about the food in hospital when you are in then contact your dietician. I had to go in for two weeks in October last year and I was offered a pass to the public restaurant to top up what I was eating. If you are worried about the high carb count then may I suggest changing to a regime that deals with carb counting? I did and I personally can eat practically anything! Take for example this lunchtime. My lunch consisted of two sandwiches and a large packet of crisps. Total carbs was around 200. My test pre evening meal had my bloods on a mere 8.5........ I am a type 1.
Robin redbreast
Thank you for your reply. It has been quite literally hell theses last few months. He was very sick and since the GF diet was started he has improved so much, which I think will help with his ability to say no to GF food when it's offered. My 10 year old daughter has also been very ill. They thought she may have had a brain tumor , with so many scary symptoms, thankfully she dies not. The GP suggested she see the Gastroenterologist as my son had been diagnosed and they confirmed she also has Coeliac disease, then they suggested my husband and I have tests and I was confirmed 3 weeks ago ( endoscopy procedure is awful)!!
We are now eating GF and my daughter is also feeling so much better and I am Losing weight so there is always a silver lining to every cloud.
As for my son, my husband and I tell him he is our hero every day. He copes so well with all that the world has thrown at him and although we all have our bad days , every day is a little better than the last.
I am now humbled by all those who deal with type 1. I just hope that I can be a good enough mother to be able to arm him with all he needs before he goes off to into the big wide world, plus also praying for a cure like everyone else I'm sure.
I am waiting to hear back from diabetes.uk as I would like to meet parents in a similar situation, I do feel very isolated by this, it has certainly showed me who of my "friends" are.
Hope you are well
Lucy
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