Bluetit1802
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Have you done any research on Methotrexate? I have seen what it has done to two of my friends.
https://www.drugs.com/sfx/methotrexate-side-effects.html
https://www.drugs.com/sfx/methotrexate-side-effects.html
Not crazy and I can understand the confusion on your part. In reality few of us type 2 get checked for which type we are. Assumptions are made and occasionally corrected later. So in a sense you’ve been lucky to get it confirmed one way or other at the beginning. Finding it all difficult to accept is also common, with or without the confusion. It passes in time so be kind to yourself. As for recommending metformin, that’s because it’s the first line (after diet) for most type 2 and others are only used of that isn’t producing the results desired or has side effects etc.That seems to be it. I don’t know how much my pancreas is working, I don’t know if I’m not producing enough or I’m producing too much and insulin resistant. I guess once that question is answered (hopefully from the GP on Wednesday) I’ll be able to accept it better. It’s the not knowing and being told different things that I’m struggling with. Am I crazy in wanting to know or should I just accept that I type 2 diabetic and ask no more??
Thanks. I have had psoriasis since I was 9 yrs old,I’m now 47, so have tried many many different treatments for it and the cyclosporin has been the only thing that’s worked, I have been on this for 10 years, now they have to swap this for methotrexate. The doctor told me that he wanted to change to metformin but didn’t go through any other treatment plan options which is why I feel a bit isolated and don’t know what’s happening
Have you done any research on Methotrexate? I have seen what it has done to two of my friends.
https://www.drugs.com/sfx/methotrexate-side-effects.html
I have done some research and have an app with the dermatologist July 5th so will know more then. What has it done to your friends? Good or bad things? I have only heard bad thing from people who have used it for arthritis
It has done "bad things" to my friends. It suppressed their immune systems, causing a lot of issues with infections, some serious. They were using it for arthritis, and were long time users of it.
That’s what I’ve heard too, so sticking with the insulin gives me reassurance and comfort knowing that one of the diseases is under control. Is this wrong?
Then once I know how the methotrexate makes me feel, I’ll think about changing. But again this is something I need to speak to the GP about as unfortunately the dr hadn’t got any notes from dermatology. I know these are all questions I should have asked the diabetic doctor but I didn’t have them as questions when I saw him
I’m not sure I’d see it as a one then the other scenario. Perhaps the dr and specialist can explain why you can only act on one at a time rather than address both issues.
Nor in your shoes right now would I see the insulin as “diabetes under control”. First aid applied more like whilst long term action to be decided.
Because some drs and nurses don’t know this, even those in diabetes care! They think type 2 is progressive and there’s nothing to be done other than take drugs. This is how it used to be seen. As progressive. This is outdated.So although treated first with insulin to bring levels down quickly because of how high they were and the ketones, over time the insulin will make the diabetes worse quicker than the tablets and diet over time? Why haven’t the nurses or doctors told me this? I suppose this is another question for Wednesday visit!!
I know I’m harping on a bit but each one of you is shedding more light on things of questions that I feel should have already been answered! Thank you
I think that’s half the problem, the DN said I was only producing some then the dr said I was insulin resistant and producing too much!! Which is it? That’s why I made an app with the GP so hopefully he can shed some light on it. I did ask the nurse after the app but she then said the same as the dr??
That’s what I’ve heard too, so sticking with the insulin gives me reassurance and comfort knowing that one of the diseases is under control. Is this wrong?
Then once I know how the methotrexate makes me feel, I’ll think about changing. But again this is something I need to speak to the GP about as unfortunately the dr hadn’t got any notes from dermatology. I know these are all questions I should have asked the diabetic doctor but I didn’t have them as questions when I saw him
So although treated first with insulin to bring levels down quickly because of how high they were and the ketones, over time the insulin will make the diabetes worse quicker than the tablets and diet over time? Why haven’t the nurses or doctors told me this? I suppose this is another question for Wednesday visit!!
Not sure as I had some bloods fasting and more taken at hospital which weren’t so not sure if this test was from the first or the second batch!!I found this which seems the same scale as your result. Was yours taken fasted? Doesn’t show where a non diabetic would fall either so not sure what a “normal” c peptide would be
View attachment 33728
It seems to make a difference whether it is fasting or random. Can you find out?