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Hi

This is probably going to sound an exceptionally stupid question but here goes...I'm 34 + 5 and still injecting into my stomach but suddenly worrying if I might be harming the baby as I am just bump, seem to have been v lucky and not put weight on anywhere else and they say at this stage baby doesn't have much room so wondering if when I inject is there any risk of me affecting the baby?

X

Hoping I think you've got it right to be honest - better to be on the low side. I was last pregnancy but have lost all my confidence with being low.

No risk at all Newbie I had the same worries last time.

Newbie was going to say same as puds i was told with my 1st needle is nowhere near big enough to reach baby, the only thing ive been advised this time round is to inject my background insulin (levemir i was changed to at 12 weeks) in to my bum as it asorbs slower from there? Seems to be working tho getting harder to reach lol

Puds would u beleive i ate a chicken curry and fried rice then a cpl squares of the diabetic choc my parents got me ( they feel sorry me craving choc lol) n at 10pm 3.9 what the hell? Waiting to test again n make sure its up a bit before i go to bed but can see a 3am high coming

Bloody hell I'm jealous! I'm having the opposite problem! I think you might just need to cut back by literally 0.2u or something and you could have it cracked...(for now). Do you have a half unit pen? Very handy. I need them as am so sensitive to changes.

No another thing i will be asking for thanks puds im getting lows but i hate them at night as to correct that one wasnt too low but could tell it was gonna keep going down i had half a diabetic turkish delight thingy and in an hour its up to 5.9 so ive set an alarm for 3am just hope it hasnt risen too far

Hi all - have been away for a week but back now. How's everyone doing? Have we had an update about baby Felix?

hoping - hello! I see you've joined our merry little gang. Haven't read back yet to see your back story, but thought I'd give you some advice about so-called 'diabetic chocolate'.

It is completely pointless. As you probably know by now, diabetes is NOT about sugar, it is about carbohydrate in all its forms which includes sugar, but also most starchy foods like potatoes, pastas and rice. These diabetic chocolates and sweets may use some sort of sugar substitute but they are very rarely low-carb. In fact, many of them use 'fruit sugars' which are just as carb-laden as regular sugar.

So, my point is, you should have some chocolate when you feel like it, but don't let yourself or your parents be ripped off into buying these crappy substitutes. They taste crap and will have about the same effect on your blood glucose levels. Just be sure that you are counting the carbs in the proper chocolate you are going to eat, take the appropriate amount of insulin and enjoy.

Here here Bona - I've just had some Lindt. Mmmmmmmmmmm.

Good to see you again Bona, I was starting to worry that something had happened!

We are home Bona have been home a week today after five days on intensive care, two in high dependably and a week in special care he is feeding well and my HV is diabetic so is not worrying about him dropping lines on weight

puds - yummy yummy yummy
diec - yes, it occurred to me while I was away that you lot might have been worried and that I ought to have warned you I was going away! oops!
spotty - that is fabulous and great news about the understanding HV!

All is fine with my wriggler. My only grumble at the moment is with my back, which is killing me!

Hi bona

Id thought as much about the choc, they were just being nice to me lol i have seen only 1 website that offers sugar free low carb snacks some of which are choc these bars have 10g carbs thinking thats good tho they r expensive! I had been having some choc with my main meal and my bg was reasonable does this mean i wasnt doing any harm to myslef??

Yep, eating after your main meal is probably the least painful way to go about it and if your BGs stay good you won't do any harm!

As long as you hits those targets Hoping eat what on earth you like! A former colleague is an old school diabetic and just could no get his head around me eating bars of chocolate (not saying you're like this Hoping but it's just reminded me). He just couldn't grasp carb counting and from when he was diagnosed he'd eaten more if less the same three meals for EVERY DAY of his life. When I'd waltz in Twirl in hand he must have thought I was totally lying about my hba1c which was in the 5s and his were always 7s. Anyhow he's going on a DAFNE course . Imagine how nice it's going to be for him eating different things!

Been anywhere nice Bona? I thought you'd gotten sick of me moaning - ha! My back is hurting too on on off. Lower back it is. Was in a panic the other day thinking it was premature labour pains

lol no no1 has ever said you cant have just that you have to cover it with insulin but the dsn i spoke to after my eye thing (who is a bit older) seemed dissaproving when i said i was low all the time and thought it was because id cut out whatever sweet thing i had- not always chocolate myb a yoghurt and now n again shock horror a cake or pudding if out somewhere but was almost always on target by next test(my consultant doesnt ask for the 2 hour post meal) so just had chicken n veg in black bean sauce with noodles took 15u as had lots n lots of noodles just ovet an hour later bam 2.4 had some jelly babies so hopefullu itl come up soon xx

Puds I'm old school too - or at least I was, I was brung up on having to eat 23 "exchanges" a day (1 exchange = 10g carbs). There was noflexibility, no adjusting doses, and no such thing as correction doses either! How times change

Mind you the MW at my joint DSN/MW appt last time I was PG nearly had a heart attack when she read my diary - I faithfully recorded the fact that I'd had 2 Cadbury's Creme Eggs for dinner the night before... and very nice they were too!

So how long since diagnosis then, ladies? I'm 28 years and counting, things have changed a bit in that time (and mostly for the better)!

Hi rue

I was diagnosed at 17 so just over 12 years officially but now looking back both me and my parents believe i was born with it to a lesser degree, i have never lived down the fact i cried for 8 hours solid as a baby and used to drink bottles of water between feeds, i then got very bad food poisoning as a child then started to put on weight hindsight is a wonderful thing.

Rue that actually sounds less stressful than the 'new' way!

Gosh 28 years. I'm a diabetic baby then. Was diagnosed at 28 and I'm 31 now. Were there any theories touted as to why you developed it Rue? What about you other ladies? I have no idea but my mum seems to remember me having a virus around the time of diagnosis. There is also a lot of auto immune disorders in my family.

Has anyone got any weird skin things? In the last year I've developed what my diabetes consultant says is granuola annulare - which I've probably totally misspelled. It's s weird red patch on my foot.

Hi

I was diagnosed when I was 13 so crikey, 24 years ago and oh how things have changed! Thanks all for the advice on injecting into my stomach

X

Puds no theorys were put forward im the only type 1 diabetic on both parents side so far as we know. My aunt has developed type 2 but is age/lifestyle related, why me

Skin is it itchy? I have had the same type of thing on one foot off and on but presumed so far its ezema as had that since i was younger.

I was diagnosed at twelve, thirteen years ago this New Year's Eve. My mum has type one too and my sister has lupus. So lots of autoimmune in the family

No not itchy Hoping but I think it can be on other people!

Spotty that's really interesting as we have lupus, under active thyroid and cystic fibrosis in ours! Maybe that is the reason....

Hmm my mum and gran on my dads side have under active thyroids i never thought that it could be related thats interesting

My sister also has graves and my little sister had problems with her kidneys which was apparently autoimmune relates oh and me and my urge sister get hives wonder if that's related?!

That's amazing! My mum and both her sisters have under active thyroids!

My sister has an under active thyroid, and my mum has developed one in the last year or so, too. I had wondered if it was all related, since its all autoimmune.