cezli84
Well-Known Member
- Messages
- 89
- Location
- llanidloes, powys
- Type of diabetes
- LADA
- Treatment type
- Insulin
- Dislikes
- needles and Diabetes!
Thank you so much everyone for taking the time to respond. My regime at the moment is novorapid fixed doses of 8 units with each meal and lantus 14 units. My diabetes specialist showed me with a dummy pen to make sure i do it correct. I started with lantus in my leg but when i mentioned about the pain, she suggested i try it in my belly. It does sting on occasions but as well as in my leg, 5mins after taking it, it hurts for a good 10mins. I think she will change me shortly to levemir. I only now use 3 fingers on both hands for bg tests and on the side not the top as i did at the start. Its taken a lot of adjusting but hopefully il get there soon, its not going to go away.
Hey scallion, glad i have helped with info although i am not knowledgable enough to give any advice, levimir is the other long lasting nyt one which they are goin to put me on in a couple of weeks so hopefully it will react better with me. Fayefaye1429 i have not even considered any creams so thank you for that, i will make a list of everything i need to equip myself as there is so much you have to think about!! I feel so alone and this group is helping. My specialist is great but i cant get in touch at any given time but here, theres always someone. Thank u everyone
Your so right, i think im just expecting to get it right from the off an i do need to understand i may do many things wrone but like u say trial and error. Everyone is different. This lantus is concerning me though, ive moved it from my leg to my tummy and still, im gettin pain 5mins after i inject. Im using the same needles as the novorapid which doesnt hurt at all. I have had my first foot appt too and have been told to moisturise a lot etc, havent had my eye appt yet but have noticed slight changes in my vision.Hey again @cezli84 sorry to hear about your difficult week but I'm glad you have found helpful information and support here on the forum.
I felt like that during the first weeks of diagnosis, that feeling that my life and personality had changed completely because of T1 diabetes. It is just getting over that initial emotional downer and then realising you can control it once you have a good understanding of some basics associated with it all. It is frustrating when you hypo and when you are trying so hard to keep good glucose levels but it will come with time. A few weeks ago I hypo'd for three nights in a row and I felt awful and yet it was something so basic as reducing my insulin that needed to be done. Even though it's not nice going through such experiences it gives us a much better understanding, and as said many times on this forum it is about trial and error to see what works best for you, your body and lifestyle
Not at all, i live in buckley, north wales. I would love to speak with ppl bout t1. I havent heard of her but will defo take a look. Thank you.I can echo what teacher has said. Do you mind me asking where you live? Just wondered if meeting other diabetics in the area might help? I wouldn't say your stubborn at all. I feel d is like grieving for what your body was. Have you heard of Elizabeth kurber Ross? She did grief stages in the 50s called the cycle of grief. It rang true with me when diagnosised so I thought I would just mention it not pressure to look at it. I just went through some time grieving for what my pancreas use to do for me but I soon found ways for me how d could benefit my life
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