In part 1 of this post I mentioned that Peyton was getting her insulin pump. She has now had it for 6 months and we have gotten used to it pretty well. I am pleased with the freedom it brings her and the fact that she doesn't need 4 shots a day. What I have been disappointed in is the lack of control over her blood sugars. The aprn that we see at Endocrinology assured me that things will level out. She is certain that her "honeymoon" phase is over (this means her pancreas is no longer producing any insulin hence the reason for her higher blood sugars and resultant a1c). She has modified her diet some but I do allow her some treats much to my mother's annoyance (she thinks she shouldn't be allowed anything but to restrict her too much is just asking for her to rebel and make things worse) but because her a1c was so high this last visit we opted not to go trick or treating. Having all that candy in the house was just too much of a temptation. We went back to endo today and her a1c had gone down a little bit so we are going in the right direction. We made a few more adjustments to her insulin and we are hopeful that things will get even better. It was encouraging to hear the nurse say it wasn't anything we were doing or not doing because I was so disappointed to see her a1c so high. Of course there's a certain amount of guilt associated there too even tho I knew we were doing everything by the book. As her mom and sole caretaker it is my job to ensure she is well cared for. To protect her and keep her healthy. To not have that control over this disease feels like a failure on my part. As unreasonable as it may be the guilt is there just the same. I've been finding myself waking up at all hours of the night just to check on her like I did when she first came into the world just to make sure she is still breathing. Then she will check her sugar and go back to bed. I am getting so paranoid but I know this child has a purpose on this planet. She is destined for greatness (i know every parent feels this way but when you have multiple school teachers say the same thing one tends to believe it) and I will do anything I can to help her achieve those goals. Who knows maybe she will be the one to find a cure for this disease. :) I am so proud of the young lady she is becoming.
Friday, November 8, 2013
Saturday, November 2, 2013
I am human, love me or hate me
Monday, April 8, 2013
Whats with all the negativity!!!
Thursday, April 4, 2013
ASD continued...
So my son and I are on the road to getting him the help that he needs. Above and beyond his weekly therapy sessions. He started his PHP program today and he really seemed to enjoy it. Wednesday he starts at his new school in a smaller class. PHP means less time at home and I'm really going to miss him but I know that he needs it and maybe he and I will start getting along better. He is so angry all the time and I just dont know why. It could be a multiple of things. I dont think its at me though, I think I'm just an easy target because he knows I wont give up on him, I wont leave him. Its still tough though. Typical discipline dosen't work so i've had to be creative and try to stay positive but I do snap at times. I am so hopeful that he snaps out of this soon and becomes the loving, sweet kid I know he is.
Sunday, March 31, 2013
Type 1 diabetes journey
Over labor day weekend 2012 my daughter was diagnosed with type 1 diabetes after she was hospitalized with diabetic ketoacidosis. In the 7 months since her diagnosis we have learned so much about this condition and the what to do and no to do's. One of the biggest things we have learned not to do is to listen to everyone around us. Some people say it isnt ok to snack others say it is fine as long as you cover the carbs with insulin... blah blah blah. My philosophy is follow the doctors orders. Thats what they get paid for and they arent going to steer us wrong. I need to tune out the nay sayers, the people who keep trying to advise me on how to raise my diabetic daughter especially since they have never had to raise a diabetic themselves. One person in particular keeps thinking that my daughter needs to be deprived of things she likes in order to stay healthy and no matter how much I tell her otherwise she refuses to hear me. It has gotten to point where the two children are not treated equally and my daughter is resenting it. To deprive a diabetic child of the things they like is to leave them open to sneaking those exact things and to rebel, thus being counter productive to being healthy in the long run. If you treat these things in moderation there is no reason why she cant have them on occasion.
Saturday, March 30, 2013
The craziest year ever
It all started in august 2011 when my dad went in the hospital for heart surgery and things have just gone downhill from there. I wont go into all the gory details only because 1) this would just end up being a longer than needed blog and 2) im not a woe is me type of person and am determined to keep it that way. But needless to say it has been the year and a half from hell. During this time I have held it all together and remained strong for everyone around me and now that things are finally settling down I am falling to pieces over it all. I can honestly say I have never been such a mess. This weekend though I am seeing a light at the end of the tunnel. Some hope. I am hesitant about hope though, it is a funny thing, because the minute I start allowing myself to hope for something I really want something else comes along to sweep it out from under me. I know, pesimissism, not my usual style. But given my recent history who can blame me. I find that few days or weeks of peace then WHAM something else happens. But heres the thing, this week I have found that after a terrible week, the worst, then I found out my aspie son finally found some success on a new med, is getting more help for his issues and had a great day at school. I may be in line for getting a bigger place in which , my son may now have his own room where he can have his own space, my daughter is getting her diabetes under control and getting her insulin pump (aka more freedom) in less then a month and both my children learned how to ride 2 wheelers today! I am so proud of them! 2 kids who are usually happy sitting inside playing video games all day could barely be brought inside for lunch. I actually forgot to give them their ADHD meds because they were using that energy constructively. So I am allowing myself some hope, for peace and for these small success' because I'm finding that while I've been so busy focusing on the negative things I'm afraid I've been letting some of these small victories pass me by. My goal for the near future allow myself to hope and see the negative things for what they really are just a learning step between victories.