Tag Archives: Sparearose. insulin

If I weren’t so lucky by Matt Butler

7 Feb

It is pretty simple……..

If my insulin was not provided for by the National Health Service from the second I was diagnosed, I would be in a lot of bother. I may even be dead. I certainly wouldn’t be married to the woman I am now.

I remember my day of diagnosis well: the nurse called me in to a small room and told me that the blood tests I’d had done did indeed confirm that I have Type 1 diabetes and I would have to inject insulin every day. As crappy as I felt (apparently I wasn’t far from being hospitalised), there was the small matter of being told to stick a needle into myself. See, at the time I could not stand needles. I still cannot watch the television if an injection is being depicted. The abject fear on my face was probably plain to see. I can’t imagine what the look on my face would have been like if the nurse had have added that every injection I did would cost me. Because when I was diagnosed I was in a pretty poorly paid job, as I was only just embarking on my journalism career. So if insulin hadn’t have been provided to me (literally there in that room, mixed 25-75 short and long-term, in a burgundy-coloured pen with a fresh shiny needle of 6 millimetres in length), I would have been faced with a pretty tough choice. Either take out crippling health insurance, pay for my insulin via unsustainable loans, or buy an air ticket home to my parents on the other side of the planet and ask them extremely nicely to fund my new needle habit. Or of course I could have just not taken it. And then died. None of the choices above would have been attractive. In fact looking at the alternatives to having insulin provided to me makes me wonder what I would have done. As well as the new world of regular blood-glucose tests, carbohydrate counting and the need for a supply of jelly babies to be kept close at hand, I’d have had to either uproot my life, take out a second job or be plunged even further into debt. Or I could have keeled over drowning in ketones.

Of course there are people in the world who do not benefit from a comprehensive state healthcare system – but still cannot afford the insulin they need to stay alive. We will ignore the accusations that pharmaceutical companies contribute to an artificially inflated insulin market, but just acknowledge the fact that insulin does cost a lot of money. And it is not as if people with diabetes have any alternative.

Spare a rose. Save a child

https://lifeforachildusa.org/

 

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My Nan’s Cat………

6 Feb

scared cat

Ok. We have all heard this at some point in our #WalkWithD when we discuss that we have Type 1 Diabetes with someone and then says………. “Oh! My Nan’s Cat had Diabetes. She had to inject it and everything………”

Note: This post is in no way meant to upset animal lovers in any way so please do not take offence. There is a very serious point to this somewhere in the post so please read on.

So.

I have heard this several times in the last 20 years since my Diagnosis, and there are a lot of pet owners and animal lovers in the UK that have a Cat, Dog, Gerbil or Goldfish (I made that one up) that unfortunately have Type1 Diabetes.

This has me thinking (really never a good thing, and, quite painful).

In the UK we do not have to pay for our insulin, for which we are very lucky and I will be forever grateful. In fact paying for medicine or medical equipment is quite alien to us and if we have to for things like CGM or Flash Glucose Monitoring we occasionally get a bit pissed off annoyed about it. Unless it’s for our pets.  If our aforementioned Cat, Dog, Gerbil or Goldfish needed insulin, then most of us would willingly pay for this in order to keep the animal that we love alive, because of course, without insulin, that pet would die.

What’s the point to this Grumpy post?

The point is this. In other countries, children are dying because they have no insulin. It is not provided, they cannot afford it. Simple as that!

If I would fund the insulin to keep my pet alive, then I should donate to #SpareARose this Valentines to help keep a child alive.

 Sparearose

The Spare a Rose Campaign is raising money to provide insulin to keep children with Type1 Diabetes in other countries alive. There is more information at http://www.p4dc.com/spare-a-rose

Please donate.

Live Long and Bolus

Grumps.