Okay, I left off our Diabetes story at the point Nikki was released from the hospital. We get home and are a feeling a mixture of relief in just being back in our own house and complete fear that we won’t be able to take care of Nikki and the worst will happen.
Of course, there is our other daughter, Amber, to consider as well. One thing that can and often does happen is that the chronic illness of one child can completely over shadow the needs and even the existence of your other child who is completely healthy. I will touch more on that in future writings, but I would like to say that Amber is another of my heros.
That first night home we slept, the 4 of us, in mine and Bryan’s bed; we just needed to be together. We made our way through the next few years. There is so much involved in the day to day living of life with diabetes that I won’t try to go overboard in details. Instead I want to touch on a few milestones.
I mentioned in the first writing Nikki’s anger toward me. That is sort of putting it mildly. I would say that in her 5 year old mind she bordered on hating me, at the time. Of course, I basically agreed with her. Her anger at having Diabetes was totally directed at her mommy. She was not capable at such a young age to identify her feelings and/or give a voice to them; so they naturally came out as anger directed at the person who she thought could fix everything, mommy. The outbursts were frequent and increased in violence. The final outburst came about a month after her diagnosis during a trip to Kroger.
We had finished our grocery shopping; Amber was at home with Daddy so it was just Nikki and I. She decided, for no particular reason (and I believe there really wasn’t one) that she was not going to get in the car with me to go home (I think she felt so out of control that she was trying to control whatever she could, namely me). Up until that point, I will admit that I indulged her anger toward me because I felt so rotten that she had this thing to deal with so I overcompensated in inappropriate ways. Anyway, she stopped about 8 feet from our car and said “I’m not going home”. I told her, most likely in a very sappy tone of voice, that we needed to get home because she had to eat. Looking back now, I believe that comment was the trigger for the total meltdown. She started trying to kick me. A light bulb went on in my head and I realized that I was losing control of my 5 year old and that having diabetes was no excuse for public temper tantrums. I picked her up. Those of you who have ever had to pick up a 5 year old in the midst of a temper tantrum have an inkling of the strenghth they can have; combine that strength with an overwhelming anger and terror at not really knowing why your parents are constantly sticking with needles, making you eat when you don’t want to, not letting you eat when you do want to, etc. etc. and you get a minature Incredible Hulk.
People stopped and stared at us; most likely convinced that I was (a) kidnapping an unwilling victim or (b) a terrible mother; at that point I didn’t care. My only objective was trying to get this little person into the car. I finally succeeded, and then it took another almost half hour to get her into the car seat. I backed out of the parking spot and began the short drive home. About halfway there Nikki managed to get herself out of the carseat and was attempting to get out of the MOVING car. I just kept going. I drove the last 2 mintues to the house with one hand on the steering wheel and one and on the door lock in the back seat, with Nikki biting my hand, and I don’t mean a nip, my hand was bleeding.
I get her home and by then yes I was fussing at her; we get inside and I just collapsed on the kitchen floor in tears. I began sobbing, really sobbing and she suddenly stopped being angry at me and just looked. After a couple of minutes I felt her little hand on my head, I looked up at her; at that moment we reconnected through our tears, we continued crying and holding on to each other. I think it was that moment that Nikki realized I hated what was happening to her as much as she did. Obviously, a 5 year doesn’t process information in that way but that was the jist of what she understood in that pocket of time.
What I learned from all of that is this: You have to be strong for your kids. To me this means not falling apart before, during or after a crisis. You don’t want your kids thinking about how mom will act once the crisis is over, that will only add to their stress. So I kept it all in. The message Nikki got from me was that I was okay with her having diabetes. She thought it didn’t matter to me. Showing and sharing our feelings with our children is a good thing when done appropriately and they need us to be human. They need to hear us tell them we are sorry when we screw up, or when they are hurting. Nikki never had another outburst after that day.
There is much more I will write on as time goes by but I want to tell one last story before I close this portion. The day after we got home from the hospital I noticed something on our front porch. I opened the door and there sat a teddy bear. Not just any teddy bear, this was a diabetes bear. Her name is Ruby and she even wears a medical bracelet. She has patches on every part of her bear body that match the places Nikki was getting injections. Her legs, hips, arms, tummy so Nikki could give her bear a shot in the same place she had just had to get one. This bear was an anchor for Nikki. So who was the mystery gift giver? Many of you know that Nikki has been dancing at The Dance Center since she was 2-1/2. All of her early dance years were spent under the teaching of Miss PattiAnn. Miss PattiAnn has a daughter named Haley whom Nikki idolizes. We found out that it was Miss PattiAnn and Haley who had left the bear (and other diabetes items) on our doorstep. You see, Miss PattiAnn and Haley also have Type 1 Juvenile Diabetes. This is one of the many ways that God has intervened on Nikki’s behalf. She immediately had someone that was involved in her daily life to hang on to.
I have a niece and a nephew with diabetes and Nikki also adores them. However, they were in another city and Nikki wasn’t able to see them as often as she did Miss PattiAnn and Haley. They have been a continuing source of support for Nikki and an inspiration in her life for many reasons. You can see pictures of them with Nikki from her diagnosis through this past year in our group album. Haley has just graduated from high school. She is moving on to New York to study fashion design and Miss PattiAnn has retired from the dance center to move into the new part of her life. Their lasting impact on our family will never be forgotten. They will always be counted as 2 of the many blessings God has bestowed upon us.
That’s it for now. Our story is to be continued……