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Showing posts with label world Diabetes Day. Show all posts
Showing posts with label world Diabetes Day. Show all posts

Sunday, 15 November 2015

3282

Yesterday, I talked about the 'T1D Looks Like Me' campaign which you can access here if you would also like to smurfify yourself.

Today, I'd like to show you what a different aspect of T1D looks like.

A year ago, on WDD2014, I started a collection, of sorts. The 'D365' project. It's not quite complete, but I thought I would share a preliminary look with everyone now that the initial collection is finished.

This is what a year with Type 1 Diabetes looks like:



125 Set Changes. 


125 times I pushed a cannula into my leg, stomach or back. That's  1 cannula every 3 days.


Some of them hurt. Alot. Some hurt for the entire 3 days they were in. We don't have any way to x-ray ourselves & find the nerve clusters before we put each cannula in.


3282



3282 Testing Strips. That's how many times I poked a sharp needle into my finger, hard enough to make them bleed. 


3282, is an average of 252 tests per month, 62 tests per week and 9 tests a day. Even when my fingers ache.



208. The number of hypoglycaemic events experienced. The number of times that my blood sugar was not high enough to sustain life long term and required immediate attention. That's 1 low blood sugar every 1.75 days. Sometimes, you can have 4 in one day, and sometimes, none for a week.

There is no way to predict a hypo (or trust me, we wouldn't have them!).

But in Diabetes land, we have this amazing tool to help us manage our diabetes. It's called CGM.

CGM is expensive. But it can stop hypos. Want to know why I was hypo free for 5 days straight? CGM. 

Think 3282 is an awful lot of pricking & poking? CGM gives my fingers a much-needed break.

I'm not holding out for a cure. I don't believe in one and I don't particularly feel like I need one. I can and do live my life just fine with my T1D. What I do want are the tools to HELP ME live with this disease, day in, day out. Like CGM. And in future, the artificial pancreas, or closed loop system, or the smart insulin patches.





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Reasons Why I'm Hypo:

The counter has been reset. I went Christmas shopping.

Saturday, 14 November 2015

WDD15

Happy World Diabetes Day everyone!!

Since the start of November, my facebook has been awash with pictures of smiling, happy, blue people. For those who don't know it, November is Smurf Awareness Month. 

Juuuust kidding. There is a reason for the blue take-over.

November is Diabetes Awareness month (and lung health awareness month too....so look that up) and today is WORLD DIABETES DAY!

This year, we T1's have adopted JDRF's campaign: 'T1D looks like Me' - putting a face to what T1D looks like:




There are a great many things that T1D looks like: Test strips, jellybeans, blood and needles. But what I think we're highlighting most is that we are just normal people. Yes, we walk among you, and you don't even know it. Acting like normal people. We eat the same foods as you. Watch the same movies. Go to social events.

Like baby showers (For a diabuddy, but hey). Where you get to eat blue themed food, just to further the spirit of WDD. 


(Yes, that is blue zero-sugar lemonade))
(...and a blue strawberry)

I feel like I filled my quota of blue. What did everyone else do for WDD this year?



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Reasons Why I'm Hypo: 

Last Hypo Incident:

5 days since last incident

Friday, 14 November 2014

T1D: A step-by-step assembly guide

Happy WDD everyone!!!

This post goes out to everyone in my life who doesn't understand what it means to be pancreatically challenged.

Type 1 Diabetes: A How To Guide

Step One: - You have just been told your pancreas has gone on permanent vacation. Please commence feelings of sadness, loneliness and despair. Mourn your dead pancreas. Continue this for a few days, weeks, months or years. Maybe forever.

Step Two - Withdraw a couple of Hundred $$ from your bank. Go to your chemist. Buy syringes, needles, insulin, testing supplies, jellybeans, ketone sticks, a sharps container. Maybe some other stuff. But these are the basics you will need to survive. DO NOT leave the chemist until all your money is spent. 

Step Three: - Learn to inject yourself with insulin and prick your fingers. The chemist probably sold you a crappy lancing device (finger-pricker). Poke your finger before and after every meal, whenever you want to drive, and before, during and after any physical activity you do (and yes, sex is a physical activity). If your fingers don't feel bruised and/or are covered in black/red dots, you aren't poking enough. Stab insulin into your stomach 5 - 7 times per day. Expect lots of bruises, lumps, red marks and pain. Occasional stinging feelings are to be expected. 

Step Four: - Try to keep blood glucose levels between 5 - 8 at all times. Ignore feelings of failure when you cannot achieve this 80% of the time. 

Step Five: - Prepare a meal. Do a complex maths equation to estimate the number of carbohydrates you are about to consume. Work out how much insulin to give yourself. Give yourself the insulin. Cross your fingers and hope that it all works out OK and you don't get hypo or hyperglycemia from miscalculation. Success rate is probably about 30% correct. Don't take it to heart, there's always next time you eat to try again.

Step Six: - Its time to exercise. Exercise helps to regulate blood sugars, so this step is important. Before you head off find a bum bag, spibelt or similar. Play tetris and try to cram your glucose meter, testing strips, lancing device, mobile phone, spare cash, keys, and juice into it. Once you have successfully attached all of these items onto your body, you can commence exercise. During & after exercise, be aware that you may experience hypoglycemia.

Step Seven:  - Prepare for bed. Please ensure you have checked your blood glucose before brushing your teeth. We do not recommend mixing OJ & toothpaste together. If blood glucose is lower than 5mmol/L, consume carbohydrate foods regardless of hunger levels. Go to bed. Lay awake for a few minutes and convince yourself you will still be alive in the morning. Set an alarm for 3am to check blood glucose levels to help ensure that you will wake up in the morning.

Step Eight: Wake up. Check blood glucose levels. Repeat Steps 3 through 7 daily for your expected life duration.


Occasionally you will need to repeat step 2, particularly if you are looking into insulin pump therapy.

Every few months you will need to add in a maintenance step (step nine).

To fully prepare for maintenance you will need to undergo a diagnostics test. See your nearest pathology laboratoty to have blood drawn for this. 

Step Nine: -  Your diabetes specialist visit is today. You have just spent all your money on Step 2. Call your parents and ask for money to see your doctor. Go to your diabetes specialist. They will focus on the things you are doing wrong, because you don't need help with the stuff you are doing right. Try not to take it to heart. Reward yourself for going with a slice of extra-chocolaty cake.



Congratulations! You have now assembled the parts required for a 'working diabetic'. Commence use of this model immediately, as it will supersede all 'working pancreas' models previously available on the market.

Thursday, 13 November 2014

#T1D4MEIS

World Diabetes Day is nearly upon us. This year, DQ (Diabetes QLD) are running the #T1D4MEIS campaign, asking people with T1D to take selfies with what T1D is for them.


What is T1D for me? It's a whole bunch of things.

Its a community. 10 finger pricks a day. Being challenged. Pushing myself harder. Dreading set change day. Getting to set change day and just refilling my reservoir instead. Being motivated. Having a better perspective on the value of good health. Blood. Pain. Tears. Sleepless nights. Lows & Highs. Doing things despite diabetes. Eating KitKats. My insulin pump. The smell of insulin in the morning. Determination. Being proud. The 5.5 dance. 2.8's. 25.7's. A big big handbag. Happiness. Sadness. "What did I do wrong?" "How the hell did I get that right?". Hope. Juice. Needles. Life.

A part of me.