Ive been dx for about 12 years reasonably well controlled but this last 18 months something has changed. Like most others I’ve had the odd blip and that was my fault entirely but at least I knew what had caused the increase. . I’m careful what fruit I eat, I really miss oranges and bananas tho , I don’t have a sweet tooth so that’s not a problem, hardly ever eat potatoes and limit the bread To the occasional sandwich . I love rice and pasta but have cauliflower rice and brown pasta which I was told was okSo they have you on fixed doses at fixed times? You say they are reluctant to change away from the fixed doses and go for rather than carb counting and dosing as required? Have they explained why? Or why they won’t do the c-peptide? That would give some strong answers as to if you are incredibly insulin resistant or if you are underproducing. Not sure how long you’ve been diagnosed but have they ruled out LADA/type 1 or done any antibody testing?
Are you confident you are aware of all the carbs and that none are sneaking in because you’re unaware of hidden ones?
If you lost muscle can you be sure you were eating enough protein? Are you able to do weight baring/strength type exercise? Carbs are not required to maintain lean muscle mass. Protein is
Ok so LADA misdiagnosis seems unlikely if diagnosed 12 yrs. Though there is nothing to stop a type 2 getting autoimmune type 1 in theory, statistically it can happen to anyone. Was there anything that preceded the lessened control? Covid maybe? I also know nothing of cerebral ataxia so cannot comment on that aspect.Ive been dx for about 12 years reasonably well controlled but this last 18 months something has changed. Like most others I’ve had the odd blip and that was my fault entirely but at least I knew what had caused the increase. . I’m careful what fruit I eat, I really miss oranges and bananas tho , I don’t have a sweet tooth so that’s not a problem, hardly ever eat potatoes and limit the bread To the occasional sandwich . I love rice and pasta but have cauliflower rice and brown pasta which I was told was ok
I cant exercise ( I realise that this would bring my BG down)very much as I have cerebral ataxia but ive just found out that this can affect diabetes so I might look into that more. I also have very little moment in my left arm due to my radius being removed. The only reason they give for not doing the cpep is that they don’t think it’s necesssay ? And I don’t think I’ve ever had any antibody testing
I used to snack on carrot sticks till I found they made my sugars go stupidly high, which surprised my DN so I snack on pecan nuts which are fine for me and a good source of protein as I know I don’t particularly like meat.
I’m a bit scared of repeatedly asking for tests as I feel as if I’m telling them how to do their job. The DN a I have at the moment seems to be taking an interest and having regular phone contact which is more that I can say for the previous one. You were lucky if she saw you for two mins
Ok so LADA misdiagnosis seems unlikely if diagnosed 12 yrs. Though there is nothing to stop a type 2 getting autoimmune type 1 in theory, statistically it can happen to anyone. Was there anything that preceded the lessened control? Covid maybe? I also know nothing of cerebral ataxia so cannot comment on that aspect.
Doing c peptide is important. If you physically cannot produce much insulin then drugs such as gliclazide are pointless. It is necessary as it shows which medications are valuable and which aren’t. Who want to take drugs that do nothing useful and have potential side effects? It also shows to some extent what effect diet can potentially have. If for example insulin production is very high then you know dietary options are available. If its non existent then it’s down to insulin injections for certain.
What about the explanation for sticking with fixed doses? They don’t seems to be working as they are set right now. They should be explaining your treatment and the rationale for it. It’s a big red flag if they can’t/won’t
Whilst I hear you that this nurse is more interested than the last my experiences and reading of others simply reinforces my belief polite but firm and evidenced insistence is the only way to navigate the nhs. Sadly those of us living the experience WILL sometime know more than some professional do. Sadly, sometimes, we do need to tell them what to do, politely but firmly.
Lots. It’s been linked to an increase in both type 1 and type 2 diagnosis. Sometimes these are unusual and temporary, more often ongoing. Whether covid is causing them, tipping them over the edge, identifying undiagnosed cases or all of the above is still being investigated. It frequently causes a rise in levels, sometimes temporary sometimes more long lasting. There’s increasing evidence infections are effecting the immune system in previously unrecognised ways.Has there been a link with covid and blood sugar?
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