My Dream
May 8, 2008
5:30am, the house is silent, I am awake. I just woke up from one of those bizarre, scary dreams, but I didn’t sit up straight with a pounding heart. Instead I calmly opened my eyes and thought, “I can do this.”
In my dream I was defending my youngest son from an attacker, some primordial reptile beast, like a crocodile. It had attached itself to his foot and I was frantically trying to get away, to push it off, to free my son. I was terrified that it had hold of him and was maiming his poor body with it’s sharp teeth. I kept calling frantically for my husband who was standing nearby to hear me, to turn around and help, because I didn’t feel I could do it by myself. As my husband finally turned around I found I was able to push the beast off and realized it wasn’t biting him at all, just holding on. As I kicked the beast out the door I also discovered that it was no longer a terrifying reptile but instead a dog, and a fluffy one at that! The dog slinked off begrudgingly and I slammed the door shut behind it, holding it shut with my own body.
I recognize that this dream represents the emotional and mental process I have gone through lately. I have experienced most of the stages of grief– denial until I made the call, anger (I still get angry sometimes), depression and the resulting overwhelming exhaustion. I am realizing I have been depressed ever since Percy received his Evaluation. It has been a very emotional experience and I have been mourning the death of what I expected, how things were supposed to be. I have had to accept that fact that my son has something going on inside him that is causing his speech delays and other concerns. I have been adjusting to a reality full of appointments and paperwork and therapy. I have also gained almost 10 pounds (well, actually I found the 10 I had lost, so at least I am breaking even!). I am now at the point that I realize I need to consider going on anti-depressants– my most recent hour-long crying spell scared me and I think I may need some help to deal with all these life changes and some of this new stress. I do not say this lightly, but I know myself and my sensitive body well enough to know that sometimes I get stuck in a down mode after periods of extreme stress and need a little help to get readjusted.
So now I am to acceptance. It has been necessary to come to accept the unknown and that I am not in control, which is so hard for a mother. Someone asked me recently, “Once he has been going to therapy for a while will he eventually catch up and be fine?” I had to honestly answer , “I don’t know”. I had to accept the frightening reality that it is possible that my son will struggle his whole life. I am not being fatalistic, I am being realistic. I hope that will not happen, but the videos I saw of children with Speech Apraxia who still struggle to talk as teenagers haunt me. I also still live in fear that one day he will disappear like all those happy, loving, talkative children who develop regressive autism and become detached. My heart breaks for those poor parents who can’t even get eye contact from their children.
But I accept that this is our life and my family can get through it together. It is hard sometimes, but it has also been a richly rewarding process. The spectre of developmental delays, of treatment, is not as frightening now that I am facing it confidently head-on and not running away. I know we are doing everything we can to help our son thrive. I know he is not broken, just unique. I also know no matter what happens we will love him. I CAN DO THIS. We can do this this together.
Entry Filed under: Autism Spectrum Disorders, Early Intervention, Parenting, children, family. Tags: Add new tag, dreams, family, fear, grief, Parenting, special needs.
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1.
feener | May 8, 2008 at 11:56 am
very well said. you are so brave. i did go on lexapro, i needed something to get me back to feeling like i could do it. i believe i have more anxiety than depression and the meds seem to be helping. i went to see a speaker last night. she is THE doc to go to for getting your child evaluated for autism/adhd/ etc. it was more geared to adhd. the parents who spoke for their children were amazing. really i felt like i was in the company of some kick ass moms. i felt as if it should have been a requirment for every parent. b/c parents who do not have a child with any special needs, need to understand how it all works as well. to teach tolerance and acceptance.
2.
thecanvasgrey | May 8, 2008 at 1:33 pm
I’m so glad God graced me with a moment and thoughts of you so I could read and catch up this afternoon. I’m propping you up in prayer and I know there are others doing the same. God provides, He really does and as it goes, you will see, your son will get great care and make great strides. See how your dream shows you the way, as you make your way through the maze the threat becomes nothing, this is so soothing to hear straight from you. God knows, now you know. God is Good! Your son is fortunate to have a “kick ass” mom (to borrow feener’s words). He is going to do well. Hugs, Deb
3.
Goldie | May 8, 2008 at 2:33 pm
you two cracked me up AND made me cry. that’s about all I can muster up to say right now. thank you.
4.
Boo Sr. | May 8, 2008 at 4:50 pm
Hugs and prayers from me, too. Sorry I haven’t gotten to talk to you this week. I’d love a phone conversation sometime if you’re able to tomorrow. As far as depression and meds, I was going to talk to you sometime about a long-time friend who had an almost intervention with me and wants me to get into counseling and possible anti-depressants. I also think they might help, not neccessarily to calm me down, but to enable me to get in gear and handle life and being a parent. So, can we try to encourage each other as we go through this period? As she pointed out, sometimes we need help from some kind of outside source to be able to be the best parent we can be. Hugs for getting all this started for the boys, and hugs for sharing it with it sounds like a supportive and encouraging audience! We can’t wait for your next chapter!
5.
fightingwindmills | May 8, 2008 at 7:08 pm
You’ve nick-named your boys after engines and it turns out that you are “the little engine that could”! I love your blog posts because I end up crying and smiling at the same time. That’s my favorite kind of moment to have among friends!
6.
gr8tful | May 9, 2008 at 3:28 pm
Let me just tell you this………..I believe FULL-HEARTLY that you can do anything you desire or need to do!! You have a way of deciding what you need to do, then you don’t let anything get in your way!! You go!!! Your a ROCK and I know you can and will get through this!!
HUGS!!!!!!!!!!!!!!!!!!!
7.
Goldie | May 10, 2008 at 8:49 pm
okay, I have some comment-catching-up to do.
*Feener, I am glad you went to the speaker. I think we all have something to learn from experiences like that no matter where our children are developmentally. And I agree that the more educated people become (and therefore more sensitive) the better.
And I think even if we doscover my children are not actually on the autism spectrum I would still look to autism research for answers because they display so many symptoms AND I think it ties in to SO many other issues. The brain and neurology are both so complex.
*CG- It feels like the terrifying monster in horror films…the one that isn’t so terrifying once it is seen in the light. Thanks for the encouragement, and even more so for the prayers.
*Dear Boo- I am not avoiding you. It has been a rough few weeks for me. We will talk soon. I am so sorry to hear you have had such a hard time recently. I think you are doing a great job being a parent…we all feel overwhelmed sometimes…or even quite often. Hang in there. I am glad you are assessing your situation with an open mind.
*FW- My goal when I write is to try and convey the full complexity of my complicated emotions. I also hope that it somehow touches, educates, enlightens, moves other people… I really appreciate it when I find out that it did indeed reach into someone’s heart, OR tickles their funny bone! Thanks for being such a great audience!
*GR8FL- Hugs back!!! Your encouragement always makes me feel like I can do anything because you always see the best in people. Thank you so much.
8.
widdleshamrock | May 12, 2008 at 6:18 pm
Yay you !!!!!
I like to say ‘be optimistic, but realistic.’
I am also on meds now, not something I took lightly either, but a very common reality amongst us mothers whose children are not average.
The journey we are on is different to those of others, but know that you do not walk it alone.
Big hugs.
9.
Goldie | May 13, 2008 at 9:46 pm
thanks widdle, i REALLY like that mantra. may I borrow?
‘be optimistic, but realistic.’
hugs back!
10. Peace and Calm « My Life As A Platypus- Goldie’s Quest for Identity | May 19, 2008 at 10:51 am
[...] minute for myself here and there. Plus we have to schedule in therapy sessions for Percy. As I realized in a recent dream, I have basically been overwhelmed ever since Percy was evaluated and began occupational and [...]