All of our hopes and dreams are gone

 (My child has Autism Specrum Disorder? Devotional #2)

Romans 8:28  God works all things together for the good of those that trust in Him.

I had to let go of the dream of getting to know all of the neighborhood moms while watching my son play ball with theirs. I had to let go of the dream of having a house filled with the friends that my son had invited over. Gone were the dreams of making new yummy treats that he would be excited to try, or checking out new restaurants as a family.

The dream of a wedding to attend, grandchildren, even just a house to visit him at faded. Gone was the certainty that someday my husband and I would have an empty nest to enjoy. The reality that my life may never change much from what it is right now, was very depressing, to say the least.

You don’t realize how many hopes and dreams you have for yourself and your children, until you are forced to let them go. You don’t realize how much of your own joy you have tied up in what you think your children will become.

The only dream I had left was the promise that God works all things out for the good of those who trust in him. He reminded me of all of the people who lived fulfilled, but very different lives, such as Mother Theresa, Amy Carmichael, and numerous other heroes of the faith. They may not have had the home in the suburbs, the 2 kids and the 7 grandkids, but they were more fulfilled than most. I just had to adjust my view from the America Dream, to God’s dream for us.

Though it was still hard to hear about how well everyone else’s son was doing in T-ball, while mine cried because he hated it so much, I actually began to feel a bit honored that God would entrust our family with the challenge of living counter-culturally in such an obvious way.

I pray that you would be able to get a glimpse of the good that God has for you in the midst of this very difficult situation. And if you can’t see any good right now, remember that God does not break His promises, so keep holding on. He will work things for good, because He promised He would.

It feels like our son has died.

(My child has Autism Specrum Disorder? Devotional #1)

Psalm 23:4  Yeah, though I walk through the valley of the shadow of death, I will fear no evil, for your rod and your staff, they comfort me.   

The son we had grown to know and love seemed to disappear. He was no longer just the bright boy who refused to use his words, the boy who had amazing hearing and a memory that wouldn’t quit and who was just too sage to speak his mind.

He was no longer just the boy with the infectious laugh that everyone couldn’t help but giggle with, even when they had no idea what was funny. Gone was the guy who just loved to shoot baskets, throw rocks into the river and roll bocce balls for hours at a time.

Our son seemed dead. Instead, we were given a boy we hardly knew. One that could talk but wouldn’t, but not just because he was being sage or stubborn, but because it was actually difficult for him. A boy who didn’t throw rocks or roll bocce balls on end just because he enjoyed it, but because he had a disability that made it difficult for him to stop and change what he was doing.

Instead of seeing our son as quirky, but whole, I now saw how broken he was. Thank goodness for my husband, who is more of a rose-colored-glasses, glass-half-full sort. I think he was able to keep a better perspective on things than I. My heart was truly broken.

Though I had suspected this reality since he was six-months old, having to come face-to-face with the fact that I would never be the mother of a “normal” son, required a lot of letting go.

The only thing that got me through this difficult time was Psalm 23. As I walked through the house I could see the deep canyons walls on either side of me. The path I was on was dark, with no sign of the valley ending. Having the promise, that God would comfort me brought me through to the other side, and it will bring you through, too.

Our worst fears are confirmed.

(You Want to Test My Kid for What? Devotional #7)

Job 3:25  What I feared has come upon me; what I dreaded has happened to me.

It wasn’t exactly surprising to us, since the specialists made it clear all along that they thought our son may have autism. But getting the actual label was quite shocking and numbing.

The specialists who tested him and who interviewed and talked with my husband and I could not have been nicer. But to be told that your precious little child has something so possibly debilitating, something with no cure, something that will not kill him, but will require him to live a normal life span under such difficult circumstances was very disheartening.

And, because of the litigious nature of our current culture, the professionals must always tell us the worst possible scenarios, and downplay the best. So we were handed page upon page describing his disability. We were told that there was only a 30 percent chance that he had a normal intelligence level. The possibility of him living independently as an adult seemed very unlikely.

It was a bit of a relief to know what the problem was, and being surrounded by a group of people who were obviously interested in helping us was comforting. But the deadening thud on our hearts could not be denied.

Thanks be to God that He does not leave us to suffer alone for long. As He eventually comforted and blessed Job, so we can trust that He will do the same for us.

We need help!

(You Want to Test My Kid for What? Devotional #6)

Jeremiah 33:3  Call upon me and I will answer you and show you great and mighty things which you know not.

Our family was at a friend’s house for a Christmas party the year our son had turned three. Within a short time of our arrival, our son was surprised by a Christmas ornament that made noise when its button was pressed. He became terrified and burst into waves of unstoppable tears. Finally, my husband decided that we needed to go home. I, being a stay-at-home-mom, panicked at the thought of needing to give up some much needed time to fellowship with others. I couldn’t bear to leave. So my husband went home without me, and I received a ride home from friends a little later on.

I know that sounds selfish and cruel, to not be willing to leave a party when my son was so obviously upset. But after three years of needing to hide myself away from anything and anyone that might upset my child, I was truly on the edge of losing my mind. My husband said that I just needed to be more careful about where I brought him, be more aware of what might set him off.

But there was no place I could bring him that wouldn’t set him off. Even staying at home and following a set routine did not bring peace. When it was time to stop playing so that we could eat lunch, he would run across the room screaming and hit me, every day, no matter what consequences I came up with.

That evening after the Christmas party fiasco I let me husband know that I could take the status quo no longer. We needed to get help on how to help our son, and there was no way to get help, if we didn’t know what the truth of his situation was. He agreed that, as much as we did not want our beautiful boy labeled, we needed to find some answers.

The next day I called our school district’s early childhood education department to let them know that we were interested in continuing the testing that we had halted a year earlier. It was a terrifying step to take. Would the return outweigh the risks?

Thankfully we have found God to be faithful in leading us down the path of having our son, “labeled.” The support we have received because of his diagnosis has been amazing.

We do NOT want him labeled!

(You Want to Test My Kid for What? Devotional #4)

Proverbs 22:1  A good name is more desirable than great riches.

My husband and I were caught in a catch 22. We were pretty sure that our son was not, “normal.” But our state won’t let anyone in their employ help our son without giving him a label, first. It makes sense that the state can’t okay the disbursement of funds unless there is documented need for those funds. But we were afraid that getting that label would fundamentally change how the world treated our son.

I suppose we could have had him tested and labeled by the school district without telling anyone we knew about it. But the label would follow him throughout his school career. Eventually word would get out. We could have chosen to have him tested by a private agency, but again, if he needed help once he became school-age, the label would have to be shared with the school district. We knew that realistically, there would be no way to keep such a label from affecting him.

We were afraid that people would consider him to be stupid, that they would not give him a chance at life, that they would make fun of him or find ways to manipulate and use him. So we decided that at two years of age, a label was not what we wanted for him.

Was it selfish on our part to not move forward with testing? Were we just too scared to deal with the implications of a label? Possibly. Do I sit and wonder what our child would be like if we had decided to get help for him earlier? No. We made the best decisions we knew how to at the time, and I believe God will honor that.

What things do you worry about should your child receive the label of, “Autism?”

Thankfully people today are much more open to treating those with differences as an important part of society, compared to previous generations where people with differences were often hid away.