There are so many things I always want to say to the world...to noone in particular, just need to get out what I'm thinking and this has always been the best way for me. So, maybe I'll start again. Maybe I'll make one or two posts and feel better and won't need it any more. Or maybe I'll make one or two posts and just realize the million other things I have to be doing and give it up. I used to be really good at follow through, keeping up with things, those days are gone.
I realized that my last post was when B turned 3. In a few short months she will be 5 so I owe a post to her. And I had a draft of a post from when January that I never finished so I just posted that too so I won't forget all these important things when I look back upon my life and wonder where the time went. It's incomplete. But it's there. The past few years have been hard. Maybe I didn't blog about them because I really didn't want to remember the details. But I remember the details, maybe not the specific week we tried a different medication or the week we went to a particular doctor, but I remember the details.
So here we go again, chronicling our life. Maybe I'll add a little more about life and not always write about the kids. Or maybe that is life so I won't have too much more to say. I don't expect anyone to read but maybe it will feel good to let it all out.
Trying to find our fun while struggling to find the best life for our son with special needs.
Friday, December 18, 2015
Wednesday, January 28, 2015
2014 - The Hardest Year Yet
2014 was a hard year for me. I spent New Year's reflecting on this year and thought a lot about how different and hard this year has been. Let me start by saying that we are lucky that everyone is fairly healthy and I am grateful for that. When Conner was a baby and in the NICU for 4 months, came home on Oxygen, had to go to therapy to learn to roll, sit, crawl, walk, talk and eat, I thought I could handle anything.
Conner's early years were hard for many reasons. He was clearly behind his peers physically and socially and his health was not the best (not terrible, just not the best). At some points, we spent 5 days a week in therapy of some kind and doctors appointments each week. At one point we were told Conner would most likely never walk. Conner didn't talk until he was 3 AT ALL and we were actually told by a doctor that if he didn't talk by age 5, he probably wouldn't talk ever. There were stressful days, doctors with no compassion, people who said uneducated things. But Conner was such a good baby, a good toddler. He smiled during therapy and for all those appointments. He did all the hard work that was asked of him at such a young age. Doctors said that his attitude was one reason why he was doing so well. He was happy and he was making progress every day so we were positive and had hope for the future. I felt confident that things would just get easier over time. And they did for a few years.
At some point during all of this, we started treating Conner for ADHD. It was pretty much impossible for him to be in a school environment without trying something. So the medication trial and errors began...and it was REALLY bad at times. We finally found something that seemed to work but the effects were short lived. After a month or two, we needed to increase and finally after about a year, we had to increase again and really we question whether some of Conner's behaviors now can be attributed to this medication. This year, we have been to more doctors' appointments than I think we have been to in the last several years combined.
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