I've been Type 1 diabetic since 1968.
I had flu in January 1968, and from googling I think it was probably H2N2 virus (Hong Kong flu came the following year).
By about May of 1968, aged 12, I was diagnosed with Diabetes (no real ditinction between types back then).
That was the end of my dream of becoming an RAF pilot.
Par for the course was urine testing, a glass syringe, massive needles in foil, and bovine insulin.
Biggest change was when I got plastic syringes, and I didn't start finger-prick testing until about 1982. Insulin was changed to porcine by then too.
I was always very hypo aware, and indeed I could tell what my blood glucose was within 1 mmol whenever I compared with a finger-prick test, so I just injected twice per day and relied on my awareness (my HbA1 tests always vindicated this regime).
In 2006 my awareness of glucose level started to fade, and it was becoming difficult to get porcine insulin, so my regime had to change.
I am now on Lantus once per day, and NovoRapid whenever I need it. I test my blood glucose very often.
I have kept all the records of my HbA1 going back to the 1980's, and although I hardly ever did much testing back then, it was always better than 8% (tht was the goal in the 80s). More recently it's 6.5%.
I have been lucky I guess, because I have no side effects, apart from slow digestion (gastroparesis) which I reckon began in about 2006 and started to become more obvious to me when I switched to Lantus and NovoRapid. I had to do a lot of searching on the internet to find out about gastroparesis, and then to convince the medical profession that this is what it was (despite a gastroparesis test showing negative).
Anyway ...
I've finally decided to join a Diabetes forum, hopefully I might be able to contribute, BUT I know that there are things I want to get more deeper knowledge of.and I think I need help in other ways too.
I had flu in January 1968, and from googling I think it was probably H2N2 virus (Hong Kong flu came the following year).
By about May of 1968, aged 12, I was diagnosed with Diabetes (no real ditinction between types back then).
That was the end of my dream of becoming an RAF pilot.
Par for the course was urine testing, a glass syringe, massive needles in foil, and bovine insulin.
Biggest change was when I got plastic syringes, and I didn't start finger-prick testing until about 1982. Insulin was changed to porcine by then too.
I was always very hypo aware, and indeed I could tell what my blood glucose was within 1 mmol whenever I compared with a finger-prick test, so I just injected twice per day and relied on my awareness (my HbA1 tests always vindicated this regime).
In 2006 my awareness of glucose level started to fade, and it was becoming difficult to get porcine insulin, so my regime had to change.
I am now on Lantus once per day, and NovoRapid whenever I need it. I test my blood glucose very often.
I have kept all the records of my HbA1 going back to the 1980's, and although I hardly ever did much testing back then, it was always better than 8% (tht was the goal in the 80s). More recently it's 6.5%.
I have been lucky I guess, because I have no side effects, apart from slow digestion (gastroparesis) which I reckon began in about 2006 and started to become more obvious to me when I switched to Lantus and NovoRapid. I had to do a lot of searching on the internet to find out about gastroparesis, and then to convince the medical profession that this is what it was (despite a gastroparesis test showing negative).
Anyway ...
I've finally decided to join a Diabetes forum, hopefully I might be able to contribute, BUT I know that there are things I want to get more deeper knowledge of.and I think I need help in other ways too.