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Showing posts with label hypo. Show all posts
Showing posts with label hypo. Show all posts

Thursday, 28 November 2013

My Diabetes - Coincidence or What? UK Newspaper Article - Why sex is good for you

I was just looking for the statistic that sex is equivalent to athletic exercise when I stumbled across this article in todays UK 'Daily Mail Online'.

The article gives ten reasons why sex is good for normal healthy people.

daily mail newspaper article Why sex good you 28th November 2013


What they didn't realise when researching this is that given a large percentage of the complications caused by or associated with diabetes are circulation related, then sex for diabetics must be even more health giving.  Lets face it, anything which increases your exercise, heart rate, carbohydrate metabolism is in my own personal experience extremely useful especially when a lot of exercise is mind numbing.

Also, depression and loneliness are frequent issues for long term diabetics, so anything which causes the release of the positive hormones and makes you feel good must help and bind you to your loved ones.

I'm not surprised that sex is good, but alas not available on Dr's prescription.

I hope you enjoy the article.

Below are Amazon UK links to one of the 1999 published book mentioned at the end of the article, and to a more recent thesis for those who like to research their topics.

                

And for USA readers, here are the Amazon links

               

I hope this does not offend peoples sensibilities no smut is intended.

TBC

Sunday, 24 November 2013

My Diabetes - How often do you as a diabetic or the diabetic your with look at their watch?

I have found over the years that it's really important when meeting new people I will be interacting with to let them know I'm diabetic.  It really helps them understand the little 'weird?' behaviours I've developed over the years as just plain common sense.  Question? How often do you as a diabetic or the diabetic your with look at their watch?

For me its very often almost whenever I mention time. So what did I think that those who didn't know I was a diabetic thought I was doing?  I didn't know so  I asked them after telling them I was diabetic, and they said things like, I thought:



  • you were a very nervous person
  • you were impatient with me or others
  • you looked like a junkie waiting for your next fix
  • you weren't interested in what I had to say
  • it was an ignorant thing to keep doing in public
  • if he keeps doing that, I'll ask him if there's somewhere he'd rather be
  • you were disrespectful to others, looking at your watch and not listening


It became apparent that without the appropriate background information they were rightly making some serious value judgements based on what they saw, which could have relationship or career limiting consequences.

Having been told this I decided that I would use my watch checking 'tick ;-)' to introduce others to my diabetes without appearing attention seeking or narcissistic.  I generally say something like:

"Sorry before we start can I just say that if you see me keep looking at my watch or the clock on the wall, it isn't because I'm bored, or I want you to shut up, end the meeting and go, its just that I am an insulin dependent diabetic and I need to eat at regular set times".  Interestingly, I find I even look at my watch when telling them or if I mention time in any way past, present or future during any conversation.

Of all of the thousands of people I've told throughout the years most have said "oh thats no problem and thanks for telling us".

I've always felt that trying to hide my diabetes is totally counter-productive if people aren't happy about it, then its their problem, but if they are unhelpful when I told them, they would certainly be no use for me in an emergency.

Learning Points:



  • I tell people I am diabetic so they understand that I am different
  • I find people are generally nosey and show interest
  • I find most people say they know somebody with diabetes, but sadly they say they don't tell people and keep falling over
  • I find they appreciate the confidence
  • I find that in a business situation it humanises me and the meeting
  • I find that people will then disclose issues of their own

TBC

Saturday, 23 November 2013

My Diabetes - Film 'Broken' starring Tim Roth ( Most Realistic Diabetic Portrayal I've seen on film)


Nearly every movie I have ever seen with a character with diabetes was awful verging on dangerous.

The typical scenario is some major event is going down e.g. a planes crashes in the desert where the is no water and certainly no carbohydrate,  and everybody is desperately trying to find the insulin to give to the 'hypo' diabetic... argh.. it would kill them quite quickly by hypo seizures, coma etc.

As I say to my friends and colleagues, if you find me in difficultly give me carbohydrates, if I perk up in 15 mins then all is well if I don't then the slightly higher sugar can be dealt with later.  Don't ever give me insulin or let me take it without testing my blood.

Don't the medical advisers to these corporations know anything about diabetes.

Then a month or so ago a close friend who also works with people with disabilities asked me to watch the British film "Broken" as she wanted my opinion.

At last a great film with an almost accurate portrayal of diabetes.

The story is quite simple with the portrayal of 'normal people in normal life' and an 11 year old insulin dependent diabetic girl called 'Skunk' (newcomer Eloise Laurence) who lives with her brother and single parent father (Tim Roth)  in an english cul-de-sac.  Like all of us we don't get to pick our neighbours and Skunk is living next to the school bullies.  Skunk also has a neighbour with a learning disability who she treats with kindness and respect, so what could go wrong?

I found the movie gripping, its portrayal of how normal life is for Skunk despite her diabetes was really positive, and the local boy with other difficulties is no harm to anybody.  But then lies and discrimination from the bullies and ignorance and intolerance cause everything to rapidly spiral out of control with devastating consequences.

I thoroughly recommend this as a film.

Here is what Amazon UK



and Amazon USA



This video deals with some adult themes so you may not be suitable for younger children, so I suggest adults watch it first before showing the kids.

Please let me know what you think if you watch it.

Malcolm


Tuesday, 19 November 2013

My Diabetes - How I Deal With Eating Out

Having explained the difficulties I have experienced with eating out the question is what I have done to try and avoid the pitfalls.  The thing to remember is that its only the carbohydrates that are the issue and have to be taken in balance with my insulin.

If its a night out my partner wants to do with her golf friends that she knows will have no real meal time, then I gracefully decline.  It's nice for the non-diabetics to have a normal mealtime without having to worry about me eating on time.

If I want or need to attend then:

  • I eat my carbohydrate allowance as a meal before going out. This is usually something very really simple, fish fingers and oven chips. 
  • I then attend the meal and eat everything that doesn't contain carbohydrates in the main course.
  • Quite often I get to eat some of the pudding, as it often arrives several hours late and about the right time for my mid evening snack.
As always I carry 3 or 4 biscuit bars (12 - 15 carbs) in my pockets and a bottle of lucozade in the car.  I always carry more carbs than I need for the event so that in the event of a breakdown etc I know I have enough to take me through to the next lunchtime. 

There have been many times when I have been told categorically that the meal will be on time, and that we will be sat down to eat by 7pm only for the fickle finger of fate to step in and mess things up.  So although I often end up paying for a meal I don't get to eat all of, its worth it for my health and my peace of mind.

Learning Points

  • Unless I'm cooking the food it may be late
  • My urgency has the potential to be an emergency if not planned for
  • I don't expect other non-diabetics to understand and even if the do they may not be in control
  • I always carry plenty of food and never leave the house without it
  • As soon as I get home I test my blood and if its high I taken an extra few units of short acting insulin to bring it back down gracefully


Friday, 15 November 2013

Exercise, Blood Sugar and Blood Pressure

Even before I was diabetic I knew that after a long run, I would look pale round the eyes despite having a red face and my hands would tremor.  This is hypoglycaemia in a non diabetic brought on by my burning of all of the bodies reserves too quickly for my body to break down its fats and other substances in the liver and muscles into usable glucose.

If I was not diabetic my body would reduce its insulin production and releases glucose for the remaining insulin to use when I start to exercise.  Insulin is like a catalyst your body needs it to break down sugars.  However as a diabetic on insulin my insulin level will be constant so if I do anything that requires extra energy, and I need to balance it with extra sugars.

Playing Squash

Before I became diabetic I liked the occasional game of tennis or squash.  I'd arranged to meet somebody, book a court, turn up with a bottle of water and play and afterwards I would have a sweet snack.

As a diabetic I can't do this:

  1. To play squash I must either reduce my insulin (to prevent me burning to much carbohydrate), this requires forward planning. 
  2. Or I drink a high carbohydrate drink before, during and after the game.
Okay thats seems simple enough, choose 1 or 2.  Unfortunately its not that simple.  In both cases diabetic control depends heavily on the reliability of your partner and the time of day of the game,

In both case if my squash partner doesn't arrive on time then I will have to begin exercising myself, i.e. go for a run in order to make up for the lack of a game.

All of the doctors have always told me to reduce my insulin before sport or heavy work that brings me out in a sweat.  I do this only very very occasionally, the reason is quite simple people are unreliable and get caught in traffic, forget or possibly decide not to bother to play.  I may also decide not to do the heavy work if the weather is too bad.  With little insulin in my blood my sugar will go high, and stay high for a long time.

So I tend to have a small mouthful of lucozade just before a game or heavy work and another just as it progresses.  For squash I am ready, if they don't turn up I have a modest bit of exercise to do, to get my blood sugar down.  If they do turn up i'm ready to play.

I also noted from observation, that with the reduced insulin plan it took me longer to recover and I noticed little in the way of physical benefits.  Whereas taking my normal insulin and topping up with high carbohydrate drinks to exercise, feels like watching a Popeye cartoon with spinach (if you don't know about Popeye type it into youtube).  My muscles swell and become more toned and my recovery time is vastly improved and my stamina lasts for days.

Warning, playing with my insulin level is not for the faint hearted and I acknowledge it can be dangerous, so I always have carbo's in my pockets and check my blood levels before and after sport for the some time.  Also tell the other person what you are planning to do and what to do if you start talking nonsense and falling around.

Learning Point

Reducing my insulin allows me to do exercise without lots of extra carbs
Eating or drinking extra carbs allows you to do extra exercise

Doing neither can lead to hypo if you exercise, or high blood sugar if you don't

TBC



Monday, 11 November 2013

My Diabetes - Angry Diabetic When Eating Out

For me, over the years,  the thing that has been guaranteed to make me edgy and angry is eating out.

I have lost count of the times when we have gone to eat out with friends. colleagues or strangers and it doesn't go to plan. The reasons are really simple for non-diabetics:
  • they don't need to worry about when they eat
  • they don't need to worry about what they eat
  • they don't need to worry about how much they eat
  • they don't need to worry if they arrive late
  • they usually want to go to the bar for a chat and drink
  • they usually want to wait until everybody has arrived before ordering
  • they don't need to worry how long they take to ponder the wine list
  • they don't worry too much over how long it takes for the food to arrive
It usually goes something like this:


  • we make sure those organising the meal out  know I am a diabetic, and we agree a time when we will be sat down and eating, for example 8pm
  • we agree that everybody will meet in the bar by 7:30pm
  • we agree we will order at the bar and be seated with starters by 8pm

Alas, the reality is often:


  • virtually nobody has arrived by 7:30pm 
  • by 8pm people are just arriving and are chatting at the bar
  • by 8:30pm we are still missing people
  • eventually everybody has arrived by 9pm and we go to sit down
As I diabetic I've been in a dilemma for 1 hour, should I eat an extra biscuit whilst waiting for the others or will they be here as they promised.  If I eat and extra biscuit I will have to leave some of the expensive food on my plate or risk having a high blood sugar.

So at 9pm we are seated at the table, then the fun begins:


  • Everybody wants to discuss the menu, should I have x, y or z
  • Then the huge wine debate breaks out
  • before we know it, its 9:30 as we place the orders
The issue we now have is the restaurant which was relatively empty at 8pm with quick kitchen response times is now running flat out with delays.  It's 10pm before the food arrives and I've been getting increasingly annoyed with the situation for the past 2 hours.

Unfortunately those that don't know me most likely think I'm a grumpy person without knowing that if we had one stuck to the plan of 7:30 meet 8pm eat we have all been happy.

Of course due to the extra carbohydrates I've eaten due to the delays and my blood sugar rising naturally as my lunchtime insulin has long since disappeared. When the food arrives I have no idea how much carbohydrate, garlic and other blood sugar changing herbs are in the food.  One thing I can be certain of is my blood will be high by the time I get home. 

Learning Points:
  • non-diabetics can eat when they want and there is nothing I can do to change it
  • with the best will in the world people get delayed
  • some people are naturally always late
  • I can never tell how long the restaurant will take to serve me
  • I have no idea what the carbohydrate level of the food is
This is a lot of unknowns.  Also, I have had a 32 year joke with Debbie, wherever we sit in a restaurant for some reason I am always the last to be served. LOL  Therefore, if I am invited out to an important meal I have to think very carefully in advance how you are going to deal with the delays.

Luckily as an insulin diabetic, if I test my blood and it is high, I can give myself some extra short acting insulin to bring it back down in a few hours. Then begin my normal routine.

TBC

Saturday, 9 November 2013

My Diabetes - My Diabetic Diagnosis

From 1977 - 1980, I trained as a Registered Mental Nurse, and had come into contact with people with diabetes, I had learned something of the history and I knew a little about the signs and symptoms. In September 1980 I became an undergraduate of Behavioural Sciences at a UK Polytechnic.

The summer of 1981 was warm, and therefore I did not immediately notice that I was drinking more than usual.  However, as the summer turned to Autumn I realised that I was beginning to look thinner than normal after having a flu jab and was drinking a lot.  I'd also found a local store that sold 'Cream Soda' a sweet drink from my youth and had begun drinking it in the summer heat to quell my thirst, but it appeared to make it worse.

By early October I really felt like I was 'dying of thirst' and it came to a head when I was in a local cafe that specialised in very large pots of tea. Shortly after it arrived on the table and without thinking I picked up the milk jug tipped it into the pot and started drinking from the pot. Debbie my partner was with me, and she looked at me and asked what was I doing and was I going to leave any for her?

I looked at the jug, looked at her and said, I have no idea what I am doing but I think I have must have diabetes mellitus.  Suddenly it all made sense.

In the school of nursing we'd been told that in the old days before urine test reagents (tablets), certain nurses and patients would taste a sample of the diabetics urine, and the sweeter it tasted the more severe was the patients hyperglycaemia 'excessive sugar in the urine'.  Knowing this trinket of knowledge, I excused myself and went off to the bathroom placed my finger it my stream of urine and tasted it. It was sweeter than the sweetest Honey and smelt heavily of the sugar puffs breakfast cereal.

I came back to the table and told Debbie I have diabetes. It was a Friday and we went straight to the Polytechnic doctor and told him what had happened and said I have diabetes mellitus.  He was polite but dismissive and said it was most likely an infection or reaction to a recent flu jab.  After some discussion he agreed to take blood or urine sample and said I was to come back the following week, and it was nothing to worry about.

By time we got back home I had urinated an embarrassing number of times and I noticed my legs felt literally like they were filled with treacle and my eyes were a little out of focus.  I said to Debbie, I don't like this I need to flush the sugars out of my bloodstream and so ate very little in the way of carbohydrates over the weekend and drank lots of water.

By Monday I was still urinating a lot, due to the large quantity of water I was drinking.  As I had very little in the way of carbohydrate intake, my urine was tasting less of sugar. When I went into the Behavioural Sciences department there seemed to be a bit of a panic on and asked a member of staff what was going on.  She informed me that they had been looking for me since Friday, that they didn't have my address and the doctor needed to see me urgently.

In the Doctors surgery, he informed me that my blood sugar on the Friday was way past coma levels and he was amazed I hadn't collapsed into coma.  I explained to him that I'd eaten virtually no carbohydrates all weekend, that I'd drank nothing but water and it was a three hike up hill from the surgery to my residence.

He took some more blood and urine, and arrange for a nurse to visit me that afternoon to give me Insulin.

My Learning Points:

1) My excessive urination without excessive drinking was an early warning sign that me kidneys were trying to flush something out of my body.

2) My excessive thirst on a cold day when I hadn't eaten lots of salty things or taken any anti-histamine tablets meant my body needed the fluid.  As my thirst was accompanied by excessive urination then it told indicated to me that I may have diabetes.

3) Tasting my urine is a quick, simple and not at all unpleasant test.  Urine is mostly sterile unless you have urine infection.  Also due to the sensitivity of the tongue to salt and sugar you need only the tiniest amount.  Normally urine is salty and insipid and never sweet if its sweet it shows the presence of sugar.

4) Had I not taken immediate action of reducing my carbohydrates to virtually nothing and drinking water, my blood sugar when have continued to rise causing me serious problems.

5) My prompt action prevented me from needing to be hospitalised with the condition.

TBC

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