I usually tell him to "suck it up!" I tease him about being a wimp and he gives me a lecture on the varying levels of pain a site causes depending on location and insertion method. This time I said nothing. I paused for a minute and watched him in awe.
He puts off changing his sites. He forgets to test. He will do anything rather than endure another injection or have blood work done. I will give him a hard time. I will tell him to deal with it. Why? Because in my head, I still see that lifeless little boy that I willed to live all those years ago. I vividly remember what life without insulin looked like. There is no option but this one.
Despite that hard line; despite "knowing" that there is no alternative, last night I allowed myself a moment to recognize how brave and strong he really is. I HATE lancing my finger. I squirm and cringe. I jump and do anything rather than voluntarily stab myself. I hate getting blood work done and will not watch and the needle enters my veins. The needle that I stuck into my son's stomach is bigger and longer than most needles I have experienced. I had an IV put in my hand about a year ago and after the nurse was done messing about, turning it, and twisting, I was almost sick to my stomach and fought to stay upright.
If I had to have infusion sets stuck in me on a regular basis, I would be an Emla addict and I would still cringe and squirm. My son used Emla for a few years, but then he decided not to bother with it any more.
I still believe that injections, insertions and lancing is a FAR better alternative to life without insulin but I also remain amazed at the pain that a person with diabetes goes through to stay alive on a daily basis. I am amazed at all that my son has gone through and he still simply takes it all in stride each day.
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