Friday, 2 November 2012

Oh, the Weirdness.


Day 2's NHBPM prompt is, "Write about the weirdest thing about your health condition?"

Upon first reading this prompt, my initial reaction was, "what isn't weird about type 1 diabetes?" At its most fundamental, it's a disease that is essentially the same in everyone (an ability of the pancreas to produce insulin), yet it shows itself so differently from day to day and person to person. What works for one person may not work for another, and what works for someone one day may not repeat itself the next.

So I thought I would pick one aspect that is perhaps more frustrating than weird, but still a regular issue in our house. Exercise.

Last year and the year before, Dylan played ice hockey. A grueling, strenuous, and highly skilled sport that demands a level of fitness and commitment that can challenge any child, and parent, let alone one with type 1 diabetes. Yet we managed. After some trial and error with temp basal rates (and different rates for practices than games), we finally found a system that worked for us. MOST of the time at least.

Then this fall Dylan decided he wanted to switch back to soccer instead, so that he could play on a team with many of his friends.

Back to square one we go. While hockey and soccer may appear similar in terms of cardiovascular fitness and physical exertion, according to Dylan's blood glucose rates, they are quite different. Well, at least we think they are. Every time we think we've got the temp basal for games figured out, his post game bg is totally different than the previous game.

So many variables are involved - what position he plays (he'll run much more playing midfield than defense, for example); what the weather is like; how much playing time he gets (dependent on the number of subs available at each game); what time of day the game begins (is it right before lunch, or 2 hrs after lunch, for example)?

After the first game of the season we were convinced we were on to something! He ran a 70% temp basal starting 15 minutes prior to the game. He drank a 750ml 10 carb electrolyte drink instead of water, and had 4 orange wedges at half-time. His post-game bg was 4.7mmol/l. Not bad. The following game I wasn't there and he forgot to run a temp basal altogether. He drank water and his post-game bg was 11.9. Wtf? Without the temp basal his bg should have been low, not high.

And so it has continued every game since then. Up and down, up and down. The weirdness of type 1 diabetes...

Thursday, 1 November 2012

Why Do I Write?



Today kicks off WEGO Health's National Health Blog Post Month, with a prompt asking, "Why do you write?" I wrote on this topic for a blog carnival earlier this year, so I've revised and re-posted my previous piece.

Why do I write about my health (my son's health) condition? My reasons for writing about my (my son's) health condition: I write for me and I write for Dylan.

I Write For Me
My blog is my journal; my diary; the place where I process my thoughts and feelings about raising a child with type 1 diabetes. There are days when I don't know what to write about, and yet once I start the words just flow out; other days I have a specific purpose for a post. Some posts are superficial, while others run much deeper. Regardless, I have become addicted to the cathartic power of writing. Not only is it an avenue for me to express my ideas, it is a tool that helps me to reflect on how I feel about diabetes and all that comes with it. 

Through blogging I have come to terms with my son's diagnosis, and feel a sense of peace that I never had before. It is no longer just about fighting for a cure. It is about accepting that this is the life we have been given. It is about understanding that each day is a gift. It is about knowing that I can choose to make the most of each and every day. It is about connecting and being part of something much bigger than myself (the DOC). And it is about making my voice heard.

I Write for Dylan
All of the above being said, this blog started because of Dylan and I will continue to fight for a cure for type 1 diabetes, for my son and for the thousands of individuals living with this disease. And until that cure is found, I will advocate and educate about type 1 diabetes at every chance I get. Why? Because I can't stop. I will never give up. It's that simple. 

A few years ago I gave a speech, at one of JDRF's Research Symposiums, in regards to why I walk with JDRF every year. I'm going to borrow a bit of it, as it can also be applied to today's topic. 

"When I ask myself why I walk (blog), I am always presented with the same image – the day Dylan was born. I think of that moment when the nurse put him in my arms and I held him for the very first time. I remember our first eye contact. That moment, be it very brief, felt like an eternity, and I could have lived in that moment forever. It was the moment that every mother is blessed with, when you realize that you love your child beyond all possibility, beyond all measure. And in that moment, your life is changed forever because everything you thought you knew about life, love, and what is important, is called into question and everything you thought you knew about yourself requires self-examination. In that moment the only thing in the world that matters in your child.

As parents we know that in loving our children we must also try to keep them safe. And when I think back to that first moment with Dylan, I know that I certainly never thought that keeping him safe would include safety from the immediate and long-term side effects of type-1 diabetes. But as long as it does, I will continue to walk – year after year after year – and I will never give up until there is a cure. I owe him that."

Visit every day in November as I tackle the daily prompts in the National Health Blog Post Month!

Wednesday, 31 October 2012

Wordless Wednesday ~ NHBPM!


National Health Blog Post Month starts tomorrow. 30 days, 30 health posts. I'm in, are you? Click the image above to sign up!

...and Happy Halloween!


Tuesday, 30 October 2012

Sending Relief to Storm Victims

We have all witnessed the devastation brought by Hurricane Sandy, though most of us via television or internet. For those who live in the areas hit by the storm, who have lost power, homes, or experienced injury as a result of the storm or its damage, I offer my deepest sympathies and pray that you find the strength and supoort to pick up the pieces and rebuild your lives.

Numerous organizations have offered, or will be offering, relief to victims of Sandy, be it in the form of food, temporary shelter, warm clothing and blankets, or medical treatment. ViSalus is one of those organizations. Between now and 11:59pm PST Friday, November 2nd, ViSalus will be directing all of their Community Challenge donations to Hurricane Sandy relief efforts. These donations are in the form of meal-replacement shakes. Each shake provides complete nutrition and is a balanced meal suitable for adults and/or children. To date, the ViSalus Community Challenge has donated over a million meals to people in need, including food banks, to after-school programs, to natural disaster relief.

Challenge yourself to make a difference. For a $24 donation, ViSalus will donate 30 meals on your behalf, and match your donation with an additional 30 meals. That means $24 will get 60 meals to those affected by Hurricane Sandy. Visit the ViSalus Community Giving page for further information, and to donate.

Thank you for your support.

Monday, 29 October 2012

Blogroll Updates


After completing a thorough review of my blogroll, I've decided to do some updating. I removed a few blogs that are no longer active or haven't been updated in the past 6 months or more. I've also been reading other bloggers lists to get ideas for new diabetes blogs to include on my roll.

That being said, I know there are tons of worthwhile diabetes blogs out there, so if you wish for me to include yours, or notice there's a great blog out there that's mysteriously absent from my list, please post a quick comment with a link to the site I should check out and I'd be happy to add it to my blogroll!

Sunday, 21 October 2012

Pumpkin Bundt Cake

Just in time for Halloween and the holiday season, this festive bundt cake was a huge hit with my family. Personally, pumpkin flavored foods are not my cup of tea, but I found myself drawn to idea of doing some pumpkin baking and giving the gourd another try. I'm so glad I did! I used the recipe below, which I adapted slightly from a recipe that appeared in Epicurious in October 2007. I also added a light glaze consisting of icing sugar, lemon juice, vanilla, and milk, to the cooled cake.

Ingredients

3 1/3 cups sifted all-purpose flour
1 1/2 teaspoons baking powder
1/4 teaspoon baking soda
3/4 teaspoon salt
2 teaspoons ground cinnamon
1 1/2 teaspoons ground nutmeg
3/4 teaspoon ground ginger
1/2 teaspoon ground allspice or mace
1/8 teaspoon ground cloves
1 1/2 cups granulated sugar
1 1/4 cups dark brown sugar, packed
1 cup canola or light olive oil
5 large eggs, at room temperature
2 cups canned unsweetened pumpkin
2/3 cup orange juice, milk, or buttermilk (I used milk)

Procedure

Position rack in lower third of oven. Preheat oven to 350°F. Prepare the pan as directed. In a medium bowl, whisk together the sifted flour, baking powder (if using), baking soda, salt and spices. Set aside.

Add the granulated sugar to the large bowl of an electric mixer and crumble in the dark brown sugar, breaking up any clumps with your fingers. Add the oil and 2 eggs and beat until blended, then beat in the remaining eggs and the pumpkin. Scrape down the bowl and beater. With the mixer on the lowest speed, alternately add the juice or milk (or buttermilk if using) and the dry ingredients. When everything is blended, scrape down the bowl, then beat a few seconds longer until the batter is smooth and creamy.

Scoop the batter into the prepared pan. Bake for 65 to 70 minutes (or for the time indicated for your altitude in the chart) or until the cake has risen, is springy to the touch and is cracked on top, and a cake tester inserted in the center comes out dry. Cool the cake in its pan on a rack for 20 to 25 minutes. Slide a knife around the pan sides and the top of the tube to release the cake. Top the cake with a foil-covered cardboard cake disk or a flat plate, invert, and lift off the pan. Cool the cake completely. Makes approximately 16 servings.

Nutritional Information (Approximate, Per Serving)
Calories 383, Fat 19.5g, Sodium 380mg, Cholesterol 26.4mg, Carbohydrates 50.2g, Dietary Fiber 2.1g, Protein 3.9g


Friday, 19 October 2012

Maze of Fear

Throw this into the mix to add a bit more fuel to a d-mom's fear. Dylan is going on a corn maze trip tonight with his class. 25 kids, ages 11 and 12, are headed out to a corn maze located about an hour from where we live. They'll enter it at dusk, and proceed to find their way out using their wits, sense of direction, and flashlights. This is a BIG maze. We went last year and it look us about an hour and a half, of steady fast walking, to get through it. The kids will start all together, but will quickly split into smaller groups. And while there are a few parents going, I am not one of them (I have to work), and my 2 "go-to" parents, that are very familiar with Dyl's diabetes and recognize his low symptoms, are not going either.

So let's put this all together: type 1 child on a pump with newly increased basal settings + excitement of 24 other kids and a nighttime adventure + 3.5 acres of corn maze to get through, aka major exercise + dark + no diabetes-knowledgeable adult supervision + a maze (potential to get lost). Am I insane letting him go? What if he has a low and he can't find anyone? There are so many "what ifs" running through my head.

I have to keep forcing myself to remember that he is almost 12. He's not a little boy anymore, and he's lived with diabetes for almost 7 years now. He recognizes his lows early on, and is very good at treating them effectively. This is one of those times when I can hold on, or let go. And I need to let go, so that he can continue to grow and take on more and more responsibility. So I'm permitting him to go and have fun with his friends, knowing that he's armed with a tester, a juice box, a bottle of dextrose tabs, and his cell phone.

An example of a local corn maze