People w/Diabetes are Amazing; People with Type 1

World Diabetes Day 2014 is Friday the 14th of November. This is the second of three installments of "People with Diabetes are Amazing!" series. The first installment was about Parents of children with diabetes.

Meeting other people with diabetes is my inspiration for living well myself with diabetes. They rock! They are so resilient. So, as we approach World Diabetes Day I thought I would celebrate how awesome people with diabetes really are.

I think all people with diabetes are amazing! Life threw us the challenge of living with diabetes at us and it made us feel that no challenge was too much. I have divided my homage into 3 groups of amazingness and next up...

People with Type 1

I actually fall into this group myself but I won't be talking about me. I want to talk about all the amazing people I've met in my support group and all the people with type 1 that I admire out there in the big, big world.

The people with type 1 that I have met over the years are so inspiring, so resilient, so defiant. I've met people who have lived 50 years with type 1, lost their sight because they happened to live with diabetes before so much was discovered about it. People who used to boil glass syringes to sterilize them before they could use them. These people still get up every day and say "no diabetes; you don't win today".

I also love to read about people with diabetes breaking through the barriers that others perceive to be around us; 

- Douglas Cairns, pilot, diabetes advocate
- Kris Freeman, Olympic Skier
- HG Wells, The famed science-fiction author who also helped set up Diabetes UK.
- Kerri Sparling, blogger, author, diabetes advocate.

I read about and am always inspired by people like;

- Stephen Clancy, professional cyclist,

- Catherine Brady, 4th time world champion kickboxer from Dundalk

- Kenneth Sweeney, former senior county footballer; Sligo

- Sierra Sandison, Miss Idaho 2014 who brought the worlds attention to type 1 diabetes.

- Ella Locke, who at 10 years old hiked the 154kms of the Scottish Highland with her dad to raise money for diabetes. 

and many, many, many, more......................

People w/Diabetes are Amazing; Parents of Children with Diabetes

World Diabetes Day 2014 is Friday the 14th of November. I didn't plan this very well but from the 1st of November until the 14th I'm hoping to have a daily diabetes awareness post on my facebook page (fingers crossed). This is the first of three installments of "People with Diabetes are Amazing!" series.

Meeting other people with diabetes is my inspiration for living well myself with diabetes. They rock! They are so resilient. So, as we approach World Diabetes Day I thought I would celebrate how awesome people with diabetes really are.

I think all people with diabetes are amazing! Life threw us the challenge of living with diabetes at us and it made us feel that no challenge was too much. I have divided my homage into 3 groups of amazingness starting with...

Type Awesome - The Parents!

I wanted to start with the people who take care of the little people with diabetes, the people who guide and mentor young people with diabetes, the people who are generally referred at Type Awesome on social media; the Parents of children with diabetes.

How difficult is it to try to figure out what is going on in someone else's body, in particular, a body so tiny he/she doesn't know how to speak yet? Parents of children with type 1 diabetes do this all day every day!

Did you know that most parents of children with type 1 diabetes seldom get a full night's sleep? I survived a couple of months of interrupted sleep with my newborns. I can't imagine doing it indefinitely. Surviving years of that takes something deep down.

Photo from  http://integrateddiabetes.com/ children-with-type-1-diabetes/

A parents worst nightmare is when something happens to their child that threatens their childhood and these parents have to find a way to get past their grief and heartbreak that their child's carefree childhood has been lost, so that they can protect what's left. It isn't easy and it's not something most parents can do alone.

And that's not even half the story; check out blogs from D-Mum, Moira McCarthy or the D-parent bloggers, such as Olly Double on Diabetes UK.

Diabetes and Mental strength

I was reading a blog entry on TypeOneNation.org by Kady Helme recently, about her trial of the artificial pancreas. I was actually really excited to read it because I had imagined that wearing the artificial pancreas would be like not having type 1 diabetes at all. Especially after listening to Aaron Kowalski, JDRF's Vice President of Treatment Therapies at the Friends For Life UK conference in Windsor.

Anyway, it is a well written piece and not at all what I was expecting. I had a "stop-me-in-my-tracks" moment though as I was reading it, where Kady used a phrase that I feel encapsulates the big struggle we face every day in living with type 1 diabetes. The "struggle" that is sometimes there a lot or sometimes there only a little. She wrote; "It wasn't until I was without the AP system that I understood what a mental burden had been lifted.  It was such a treat to have something monitoring my sugar levels every five minutes and reacting to it. I only really had to focus on T1D at mealtimes."

We have lots of daily tasks that we need to do to live well with diabetes and that's what most people think is the difficult part of living with Type 1. But really, the finger sticks and injections are just small things in the big picture. Its what's going through our minds as we continue on with our day beyond the time it takes to complete those tasks. The "what if's", the toing and froing of the guesswork, the checklist of questions we have to go through before we make a decision on how much insulin to take. Questions like; when did I last take insulin and what did I eat at that time? Have I been active this morning? What am I going to do this afternoon, is it going to be active? When am I having my next meal? Will I have time to eat?

Any treatment for type 1 diabetes that can lift that mental burden even just a little is as good as a cure to me.

Diabetes De-Cluttering

I am a house wife! And as a housewife I, sometimes, while in the middle of doing one task, will immediately decide another task is more important and switch. I don't know how I ended up on my knees, on the floor of my bedroom wardrobe but I did, and that's when I noticed once again my emergency diabetes supply stash. You know the back up meter that never gets used, the needles for Novapens, old meter cases in case some day another meter fits into it or just in case the current meter case gets something gross spilled on it. You get the idea. I even have my old record books and my old Long Term Illness book from before I moved to the states and came back (hint 8 years ago). Those I keep as mementos or for posterity - "Look, what I used to do back then"

Anyway, I performed a de-cluttering of old meter cases and old, out of date meters. Here's what I recycled; The Accu-Chek Compact Plus was a meter I got in 2002! Meters have evolved so much that there is no point letting the ones that I, or anyone else, will ever use, take up space.

This is the nice little pile I have left. (Note, I am not showing the stack of record books on the shelf below.)

However, I have a number of other "piles" of diabetes supplies all around the house that need a bit of de-cluttering.

#walkwithD

My Night-time Basal Rate Tests

Basal insulin refers to our background insulin; the insulin our body needs when we are not eating. People who are on multiple daily injections (MDI) would have their basal insulin in the form of Lantus or Levemir. People on insulin pumps divide their day into sections and would programme their pump to deliver their basal insulin at different rates during the day.

For instance I have divided my day into midnight to 4am, 4am to 7am, 7am to 12pm, and so on. I have programmed my insulin pump to deliver my insulin at different rates for all of those times.

I perform basal rate tests when my blood glucose readings go a bit mental and persist in being mental. My fasting blood glucose have been acting up for a couple of weeks now and I decided that it was time I figured out why.

So, I tested at 10pm, before going to bed, which is normal for me. My result was 6.7mmol, great! So, I'm all set.  I set my alarm for midnight for my next test and fell asleep pretty quickly. The tests followed every 2 hours and results were 5.8, 5,4, 6.3 and 6.1. WHAT!!! I couldn't have wished for better readings.

Initially, I thought to myself that I had just put myself through an interrupted nights sleep for no reason. But the results are telling me that my nights are not the problem and that I need to look at my basal rates for during the day. The thought of doing this is more stressful because it involves skipping a meal and during the day I take care of my children. I'm nervous about both of those things.

However, Joe Solowiejczyk suggested that my husband could help out a little with the driving and the children so that I didn't panic too much about it. I think I'm mostly worried about driving under 5mmols. Then, in the last month my husband has been travelling on a weekly basis.

So, it looks like I'm just going to have to "man-up" and practice lots of deep breathing.

More information on Basal Rate Testing can be found here; http://www.diabetesselfmanagement.com/articles/insulin/getting_down_to_basals/all/

Am I hiding my diabetes?

I've been a person with type 1 diabetes for over 21 years. And some days it seems that I don't have any interest other than diabetes. I read ALL the blogs and participate in a number of Facebook groups, I subscribe to Diabetes Daily, A Sweet Life, Insulin Nation, and many, many more. I volunteer with my local Diabetes Ireland group and organise my support group.

But, recently, I feel like I'm hiding my diabetes!?!

While my daughter attends her piano lessons, I wait outside the class with my son. I chat to another Mum whose children go to my children's school. During my daughter's lesson my insulin pump vibrates to remind me that it's two hours since my lunchtime insulin bolus and it's time to check my blood glucose again.

I turn it off rather than test in front of this mum. It's not because of the mum; she's really nice and I admire her a lot (raising 5 children and completing her HDip!!), it's because as soon as I take out that glucose meter I know what we are going to talk about. And I'm tired, and I have had my afternoon caffeine.

I'm surprised that I do this, I didn't plan it. Then, I thought about my Friday morning coffee meet-up and I've chosen not to do blood sugar tests in front of them either for the same reason. I had decided that I didn't want to be that person, you know, the diabetic. But also I think I need to have diabetes-free time.

I know it will come out eventually but for now I enjoy talking about everything other than diabetes with all of these interesting people. Diabetes is part of me, a significant part but it's not all of me.