I was diagnosed in June (exactly 1 month after my father died with Type 2 as one of the causes on his death certificate).
I was given the go ahead to intermittent fast by my diabetes practice nurse (I do 20:4 but it’s quite brutal!) and really throttling my carb intake.
I’m now hovering just above the ‘pre-diabetic’ HbA1C of 42; my first HbA1C was 72.
I bought myself a blood glucose monitor (the NHS have a recommended list) & pay for my own lancets & test strips, but I’ve found regular testing has been vital in bringing my diabetes under control. I am also prescribed Metformin (the Met shits may have been a great factor in much needed rapid weight loss 😂). My GP also prescribed Atorvastatin alongside the Metformin (nurse said it’s standard practice at her clinic).
I saw the harm Type 2 did to my father (who refused to do anything to get his under control); amputations, vascular surgeries, rampant infections, gangrene (that’s a smell that keeps on giving, the med photographer must’ve had a cast iron stomach taking photos of his rotting feet!). Dad was the true poster kid of ‘How not to handle type 2 diabetes’. Even though I had no symptoms & changing my diet to try to avoid it, genetics hit me with the diabetes stick, and here we are!
I was also given a huge booklet by my diabetes nurse all about lifestyle changes. Our Trust offer workshops to discuss how to help manage your diabetes.
There’s also a lot of useful information & advice on the diabetes.org.uk website.
My son’s Dad has type 2 & is now insulin dependant (even with metformin & lifestyle management), but that was many years after his diabetes journey started. He’s been a brilliant ally in supporting me (the last time we’d seen each other was at our son’s graduation 4 years before lol). In fact my husband was the one that suggested I talk to
him lol!
Good luck in your journey.