I'm determined not to let it beat me, if the complications do not arrive for 20 years I'll be 90 and probably won't care. I'm still a bit annoyed that I was immediately put on Metformin without the chance of changing my diet. I have suffered for many years with cysts which is a pointer to diabetes so I have had far too many tests over the last 40 years and it's taken this long to arrive. Just a last word, my OH has seen my weight drop since going LCHF and he is now joining me, looks like my son will be getting a bit of food from the freezer.
For me the jury is not out... there's good research evidence of the many benefits of metformin, and the side effects and risks are minimal for most people (we just hear about stomach and bowel issues a lot here). In contrast, I think every other diabetes drug except insulin has unacceptable side effects and risks. I base this on what I have read at Blood Sugar 101, which is based on extensive research.I was pleased I was put on Metformin.
The way I see it, it's the diabetes that gives the complications, not the tablets.
So the sooner I get the diabetes under control, the longer it takes for any complications to manifest themselves.
So, day 1, diagnosis, get the HBA1C down, by drugs if that works.
Then get the diet sorted, and kick the drugs into touch, or at least greatly reduced.
The jury's out on whether Metforin is good or bad.
But it beats spending months with high BS trying to get the diet to work, and increasing the chance of complications.
Unless you have a reason why drugs will actually make your diabetes worse that you can share?
For me the jury is not out... there's good research evidence of the many benefits of metformin, and the side effects and risks are minimal for most people (we just hear about stomach and bowel issues a lot here). In contrast, I think every other diabetes drug except insulin has unacceptable side effects and risks. I base this on what I have read at Blood Sugar 101, which is based on extensive research.
I think if a person with T2 can get their BGs down quickly with diet and exercise, and they are not overweight or a woman with PCOS, then they probably don't need metformin. It does have cancer protective effects though.
The fact is we don't know the real facts because the official line of the medical mafia occupies such an entrenched position there is not a snowballs chance in hell that reliable statistics will come out.
My personal outlook is if my average BGL as measured on my meter ( incliding any obviously false high readings) stays very close to our below 6 I am doing OK.
I agree, if given the choice between stuff-up and conspiracy, it's usually a stuff-up. I think the NHS advice is incorrect because there has not been enough momentum to consider the latest research yet, and old habits die hard.I have no reason to doubt the facts published, I don't buy into the conspiracy theory that the NHS is out to do me harm.
Timely posting for me as this is my elephant in the room I've really not gone anywhere near yet. Just trying to get my stuff together and see where I am over the next couple of years following diagnosis and adjustments.I receive the "Type 2 and you" newsletter from The Independent Diabetes Trust. Today, the September, issue 24, landed on my doormat. Having just read it, I am distressed & disturbed by what has been written. And I quote: "On average, people with Type 2 diabetes will need to start taking insulin seven years after diagnosis." I had NO idea that this is my future with this **** disease. It's frightening.
The article on Diabetic Retinopathy States "After 20 years of Diabetes, nearly all patients with Type 1 diabetes and >60% of patients with Type 2 diabetes will have some degree of retinopathy." Again, this frightens & saddens me. Of course, I know about diabetic complications. I made it my business to educate & inform myself, via this forum and other resources, when I was diagnosed earlier this year. Am I really so naive not to be aware of this prognosis. I'm angry! Rightly or wrongly so.
The Independent Diabetes Trust is a competent, trustworthy & reliable organisation with a good reputation, who educate and support those with this disease. I've no reason not to believe their statistics. I'm gutted to be honest.
All advice, views, personal experience & opinions will be gratefully received. Oh, and here's a link to the newsletter.
http://iddt.org/wp-content/uploads/2015/09/Type2andYou-Sep2015.pdf
If we were in church I'd shout "Amen " to thatI don't believe anything is inevitable.
We must have the opportunity to change the outcome, to some degree at least.
We are all empowered by what we read, the support and experiences of others on a similar road to ourselves. I'm going to fight to make sure I do everything I can to take control of this disease, as will you and many others.
The only thing that is inevitable, is the outcome if you do nothing to change it.
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