It seemed odd.
Somewhat out of place.
Why would anyone CELEBRATE the day they were diagnosed with this relentless disease?
As I pondered that notion, I realized that without the diagnosis - we would have lost our precious little Selah. Many families have experienced this devastation. Misdiagnosis, leading to diabetic ketoacidosis, and eventually death.
So, there's that.
We can celebrate LIFE.
|The night we took her to the ER with|
blood glucose readings over 600.
|Driving the next morning to Denver for our |
day long crash course in everything diabetes.
I decided yes, we will celebrate 'Diaversaries' for that very reason.
There is much to celebrate.
As this first diaversary approached there were many mixed emotions.
It is still difficult to accept that my little girl will have to live with this disease every minute of every day for the rest of her life. There are no 'breaks'. No remissions. No vacations. No time outs. It's an all or nothing event. She can't decide 'I don't feel like counting carbs today.' Or, 'I'm tired of the pokes and pricks, I'll just sit this week out.'
Such decisions will have dire ramifications for her health.
I struggle with all the knowledge I have of the devastation type 1 diabetes can ravish upon it's victims.
At the same time, I am overjoyed that we knew the symptoms; we received the diagnosis; we began the daily regime of insulin that keeps her little body healthy, functioning, alive.
|What a difference 6 months can make.|
Insulin = life
|So much life. So much laughter. So much love.|
We celebrate the victory over the death sentence that could have been. We celebrate the improved health now that she has the energy she needs from the food she eats. We celebrate her smile; her laugh; her growth. We celebrate the triumphs we experience each day as we continue to strive toward keeping her little body healthy and alive.
We celebrate...... SELAH!!!
|Pink, full cheeks. LIFE! Growth. Health.|