An open letter to our friends, family, neighbors, teachers, doctors......
Thank you all for standing by us through the last seven months of surgeries and therapies and testing and all the other things that come with parenting special and medical needs kids. We could not have walked this tough road without your love & support.
There are some things that I would like to share with you so you can better walk along side of us - now that the honeymoon phase of "adopting an older child" is over.
1) If it appears that our child is "getting away with things", she may be. We are parenting a child with a severe trauma background, and when she mis-behaves or acts out (up), it is our signal that she is feeling unsafe. Our primary job right now it to install a feeling of safety into a life that has felt unsafe for 8 years. So if she yells in my face or smacks my arm, and I bend over and take her in my arms and hold her, I am not ignoring the behavior - I am addressing her deep need (whatever it is at that time). Please don't roll your eyes or shake your head at me that I am cultivating a child who will be disrespectful.
2) I am not spoiling my child by giving her what she wants. I am teaching her to trust me because I am giving her what she needs. If she wants an egg for breakfast and I am out, I am likely to call you and ask to borrow one. Please don't hint that I could be doing otherwise but am catering to her every whim instead. You would not deny your 7 month old the formula they like or the rice cereal - it's the same thing. She has a need for an egg, I am meeting this little need so she will trust me with the big ones - like love and safety.
3) Your child has tantrums or fits, my child rages - and there is a difference. My child doesn't just "throw a fit" or "have a tantrum", she rages. For hours at times. Please don't pretend they are the same thing. They aren't. It minimizes the depth of her pain and our agony about them when you act like your child and their meltdowns are at the same level. She has more than 8 years of anger and pain stored up inside her - it is going to take more than a little crying to get it out.
4) Please don't assume a simple medical procedure or doctor appointment is simple to her. It is not. It can be a trigger for very deep rooted fears. It can be the tipping point in a hard day. It can be a reminder of abandonment, abuse and neglect. Do not rush us through your office, do not talk to about her as if she is not there. If I tell you about her - listen to me and do not make me defend what I know to be the best thing for her.
5) What you think is important may not be. I will not fight battles about homework, proper oral hygiene, or between meal snacking. I will not ask her to do things that are not important or that make her feel badly about herself. I will major in the majors right now - keeping her safe and teaching her to trust. If what you need from her creates barriers to that, your needs will not get met, because my job right now is to make sure her needs are filled not yours.
6) When we turn down the invitation to a birthday party, Disneyland or other big event, we are not denying her, we are protecting her. Nights away from home can set her back weeks. Please don't question that decision or make us feel badly.She can not handle the over stimulation of those events and it takes her days to recover. If you want to play with us, invite just us to your house for an afternoon (or better yet - invite just her so I can get an hour or two of respite). We don't need excitement and thrills, we need calm and stable.
This is a long and hard journey for our family; but we are doing God's work in her life. We are prepared to do what it takes to help her heal inside as well as outside, and the inside damage is deep. More than with any of our other children, we are learning that we are deeply dependent upon the grace and kindness of those in our lives to help us. As you help us, you are also participating in God's work in her life. Stay the course with us - even though it looks different; we need you.