Our family's "elephant in the room" is a pink one. Our 3 year old daughter was diagnosed with Type 1 Diabetes in January 2011 at the age of 2 1/2 years old, and it has changed our lives forever. Every season, I post a little update on how we are coping with her condition.
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It's been nearly six months since my last pink elephant post. I didn't intend to stay away from it for this long, it just sort of happened that way. Life is like that, I suppose.
Many, many times I began this post, only to shrug my shoulders and think, "Oh, that is nothing new. That is kind of boring." However, if you are not living with a child with T1D, it is new. It may be interesting, it may be redundant, it may be sad/funny/challenging/overwhelming/defeating/triumphing...but boring...nope, not boring, that's for sure!
I get asked about Sunshine's condition fairly frequently, which I don't mind at all. In fact, I think of it as an opportunity to bring some awareness to what Type 1 Diabetes is all about. There is so much confusion between that and the more prominent Type 2 Diabetes ~ the one mostly adults develop largely as a result of poor diet and lack of exercise. (I must admit, I don't know much about Type 2 Diabetes just that it is usually not life-threatening like Type 1). Unfortunately, most people group the two types together into "diabetes" and most of us T1D mamas don't like that as Type 2 is largely preventable, some say even curable. Type 1 is not. It is for life. It is a daily struggle to keep your child alive. Some days may be easier than others, but every day is a new day, and the threat lingers or looms ~ always.
Many people begin by asking me if Sunshine has a "bad" case of diabetes. It is a question that I may have asked a year and a half ago, before T1D moved in. Sadly, there is no such thing as a bad case or a mild case. Type 1 Diabetes is life threatening for every child (who becomes an adult) living with it. They all need insulin to survive. They all need to count the carbs in every morsel of food they eat. They all need to have injections by syringes or insulin pumps. They all need to be very mindful of the exercise they do ~ even swinging on their swingset or walking up the hill in their backyard. They all need to carry an emergency kit with them that can save their life at any moment. They all need to be monitored several times a day (we do about 20 finger pokes for her blood glucose each day ~ more than most, but it ensures we know where Sunshine is at). This includes waking up in the middle of the night, two to three times, to make sure her blood glucose is in a safe zone. Then we wake up and do it all over again.
Another common question is "are things getting better for Sunshine and your family...is life settling down?" Well, that's a tricky one because like I wrote above, every day is a new day with potential for good (BG) numbers and also for bad numbers. Good numbers means a happier day with mellower moods. Bad numbers means temper tantrums, stomach aches, and general miserableness. We are just getting used to this crazy roller coaster a little more. Perhaps Sunshine's BG numbers are slightly more in range, but this changes roughly every two weeks as her body goes through growth spurts and then insulin levels need to be played with again. It is not an exact science...far from it. More like trial and error.
The other day, the children and I went to a friend's greenhouse and nursery to get some flowers for the garden. My friend, who happens to be a yoga teacher, asked me how Sunshine was doing. I told her that more and more I see glimpses of the girl behind the disease. The girl who giggles hysterically with her brothers. The girl who loves speed and snails and silliness. I mentioned that I wondered what her life would have been like if she hadn't had Type 1 Diabetes. And my friend, my wise friend, grabbed my arm and looked earnestly into my eyes (and soul) and said, "Jules, this is the life she chose. This is who she was meant to be. Let that go."
Thank you, for that. 'Tis absolutely true.
This is my daughter, Sunshine. She's pretty wonderful. And she carries on with such determination, and it's all I can do to keep up with her. I love her so!
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On June 10th, we are walking for a cure for Type 1 Diabetes under the team name, Sunshine for Summer. If anyone is interested in donating any money to finding a cure for this condition, please click on the link to our fundraising page. Thank you so much!!!

