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Last Saturday Pastor Bud was preaching for Pastor Jason.  He was helping us see the importance and beauty of worship, including families worshiping together in church.

Paul, however, was determined to have his say as well.  So Dianne moved away from where we were sitting to lessen the disturbance he was making.  That isn’t too unusual for us.

(I must pause here and give a shout-out to my church and their training of their volunteers.  We don’t normally attend on Saturdays, so we aren’t as well known to the regular Saturday attenders.  A young woman who was serving as a greeter/usher approached me after Dianne made the shift to let me know that Paul was very welcome where we were sitting and not to worry about it.  That felt good!)

But Paul was unusually ‘gifted’ in volume this evening! As Paul’s volume rose Dianne felt the need for another solution.

So she put him in a closet.

Before you call child welfare on us, this is a large coat closet at the back of the commons area that, being summer, wasn’t being used.  Dianne could sit where she could see Paul and where she could hear the sermon, but Paul’s vocalizing was significantly muted.  He was perfectly safe and she was MUCH more comfortable.

As she exited the closet, Pastor Bud was just getting to his point about restless children sometimes needing to be taken from the sanctuary, and he allowed that it isn’t always clear when this is the best thing to do.  Dianne thought to herself, nor is it clear when it is best to put the boy in the closet!

She tells the story much better than I can write it! I was laughing so hard when she told me after the service that tears came to my eyes.  We caught up with Pastor Bud and his wife, Lisa, after the service and told them the story. They enjoyed it as well.

You might be thinking, was this really the best solution? There are usually many different ways to handle a situation like that; there were other options. But in the moment that wasn’t too bad!

I appreciate that God has created the kind of culture at Bethlehem where behavioral expectations for children can be articulated and parents can be both exhorted and encouraged in their roles. Yet when one of God’s unusually-created human beings shows up, we have the grace (and the space) to welcome them and to let parents do some creative things outside of the norm, sometimes on the fly.

Not perfectly, of course.  But on this particular evening we went home a happy family, well served by our Pastor Bud and by our church, and grateful to God for his unusual help with a very noisy boy.

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Barb Dittrich of Snappin’ Ministries (Special Needs Parents Network), my friend and a fellow parent in this life of disability, asked me to contribute to their devotional blog in honor of Father’s Day.  Below is an excerpt.  You can read the entire post here.

But exhort one another every day, as long as it is called “today,” that none of you may be hardened by the deceitfulness of sin. (Hebrews 3:13, ESV)

If you’re a man reading this blog, you’re probably a dad of a child with a disability.  And if you’re like most of us dads, you didn’t choose this life. I’m guessing it is harder than anything you’ve ever experienced before.

You’re not alone.

I remember feeling alone, especially in those early months.  Nobody understood what it was really like, it seemed.  A social worker invited us to a parent meeting and that was even worse – they understood, but they were all so sad or angry or resigned to life. We didn’t go back to that parent group.

Those were dark days, made even darker when I realized the doctors and specialists and educators thought dads were mostly there as a checkbook and an insurance card.

And Father’s Day?  All those happy images of dads playing ball with their sons or fishing or just enjoying each other’s company certainly didn’t apply to my situation.

But God gave me a gift that I wasn’t asking for.  His name was Karl.

You can read the rest here.

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Does God really use the frustrating little things in our lives for our good?  Is repeating the same songs or verses to a child with severe disabilities really worth it?

And are those two questions related?

The team at Desiring God has developed a daily devotional created from the vast library of resources from Pastor John.  You can access it via apps for Apple and Android or through a website called Solid Joys.

What follows is the devotional for today, May 25, entitled God’s Design in Detours.  Please be tolerant of the old language signifying cognitive disabilities that was used;  it was meant simply to describe the child’s circumstances and not diminish her worth as a human being:

And whatever you do, in word or deed, do everything in the name of the Lord Jesus, giving thanks to God the Father through him. (Colossians 3:17)

Have you ever wondered what God is doing while you are looking in the wrong place for something you lost and needed very badly? He knows exactly where it is, and he is letting you look in the wrong place.

I once needed a quote for a new edition of my book Desiring God. I knew I had read it in Richard Wurmbrand. I thought it was in his devotional book, Reaching Toward the Heights. I could almost see it on the right hand side of the facing pages. But I couldn’t find it.

But while I was looking, I was riveted on one page, the devotional for November 30. As I read it, I said, “This is one of the reasons I have had to keep looking for my quote.” Here was a story, not for me, but for parents of broken children.

Having broken children is like looking in the wrong place for what you have lost and cannot find. Why? Why? Why? This was the unplanned reward of “wasted” moments.

In a home for retarded children, Catherine was nurtured twenty years. The child had been [mentally handicapped] from the beginning and had never spoken a word, but only vegetated. She either gazed quietly at the walls or made distorted movements. To eat, to drink, to sleep, were her whole life. She seemed not to participate at all in what happened around her. A leg had to be amputated. The staff wished Cathy well and hoped that the Lord would soon take her to Himself.

One day the doctor called the director to come quickly. Catherine was dying. When both entered the room, they could not believe their senses. Catherine was singing Christian hymns she had heard and had picked up, just those suitable for death beds. She repeated over and over again the German song, “Where does the soul find its fatherland, its rest?” She sang for half an hour with transfigured face, then she passed away quietly. (Taken from The Best Is Still to Come, Wuppertal: Sonne und Shild)

Is anything that is done in the name of Christ really wasted?

My frustrated, futile search for what I thought I needed was not wasted. Singing to this disabled child was not wasted. And your agonizing, unplanned detour is not a waste — not if you look to the Lord for his unexpected work, and do what you must do in his name (Colossians 3:17). The Lord works for those who wait for him (Isaiah 64:4).

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This was first posted on July 30, 2009 on a different blogging platform.

Continuing on the theme,things people say to us,” Dianne offers the most annoying thing people say to her:

“God only gives these special children to special people.”

There is a lot right about that statement.  God clearly, in his sovereignty, gave us our boy.

And I don’t get too bothered by the term ‘special children.’  It is a sanitized way of saying that our children with disabilities are different than children without disabilities, usually in ways that are observable and measurable.  Given the kinds of terms used to describe our children in past times, special isn’t too bad. 

So why is my wife annoyed by that phrase?  In her own words, “I’m not special.”  She does not consider herself unusual, and doesn’t like people assuming that she is.  That attitude that somehow she is ‘special’ actually creates barriers to developing relationships.

Now, of course, everyone is uniquely created by God and has been given a purpose for existing.  Psalm 139:16 adds that our days were formed specifically for us by God even before there were days. 

And C.S. Lewis colorfully points out how unaware we are of what people will ultimately be like:

It is a serious thing to live in a society of possible gods and goddesses to remember that the dullest and most uninteresting person you may talk to may one day be a creature which, if you saw it now, you would be strongly tempted to worship, or else a horror and corruption such as you now meet if at all only in a nightmare.  C.S. Lewis, The Weight of Glory, p. 45

If only people meant that when they use the word special!  But they don’t. 

Referencing parents as special implies that children with disabilities were given parents with unusual abilities.  If only that were true!  I wouldn’t mind having some special abilities as a dad, but I certainly have made all the same dumb mistakes (and more) as other dads.  And given the rate of abortion of children with disabilities, those parents don’t feel too special or capable, either.

It also implies that this opportunity to parent a child with a disability was earned somehow – that God was looking around and saw how ‘special’ we are and decided our children with disabilities deserved someone so special.  Back to Dianne’s point:  we’re not special, with the possible exception that these circumstances give us the unusual ability to see how dependent on God we are, or should be.  

God doesn’t give us our children because we are special.  He does so because HE is special!

So, how to respond in this circumstance that doesn’t wound and maybe helps instruct?  How do we demonstrate confidence that “The Lord is righteous in all his ways and kind in all his works” (Psalm 145:17) and depending on him in hard circumstances is a good thing? 

I’m still working on that one, but here’s what I’ve come up with so far:

I love that you see my son as having inherent, God-given value; I certainly think so!  But God made me just like he made you – there’s nothing unusual about me. God has promised to supply what I need, and that’s true for you as well if you cling to Jesus.

What do you think? 

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Earlier today a judge declared that I could still be Paul’s father.

Well, not exactly. He granted our petition for guardianship, which means Dianne and I have the legal authority and responsibility to make decisions for him as he transitions into adulthood.  In other words, we get to keep doing what we’ve been doing all along, only now we have to submit a report once a year that we’re still taking care of him.

I learned a few things along the way:

  1. Ramsey County takes this really seriously.  I’m glad for that as taking away someone’s civil rights should be taken seriously.
  2. Having multiple severe disabilities made this process really easy.  Everyone who was notified immediately agreed that Paul should be a ward, and that his parents should be his guardians.
  3. Parents out ahead of us in this complicated life are really, really helpful. I knew that already, but was reminded again that even after 17+ years, there is so much I don’t know.  Dianne talked to some moms, and Mary Horning recommended the attorney we used which made everything easier.

All in all, the process went without any complications.

Yet there were parts that just felt weird. We had strangers come to my home, one on behalf of the court and an attorney assigned to represent Paul, to ask Paul questions and determine if he was in an appropriate living situation.  They were both very pleasant men who had quite a bit of experience with these things; neither one was in the least disturbed by Paul’s behaviors or his lack of response to their questions.  But knowing they could independently make the process of our having the legal right and responsibility to take care of our son, as we have done since he was born, more difficult based on their assessments from just a single meeting was unnerving.

And after I was sworn in by the clerk and the two attorneys asked me their questions, I realized the judge’s decision is still based on trust.

If we needed to, we could have gotten dozens, maybe hundreds, of people to speak to our care for our son and our character.  We have more doctors than I can name who can document all the ‘stuff’ we’ve done over the years.  The school systems has 17 years worth of IFSP and IEP meetings in their files.

But that doesn’t mean we’ll do in the future what we’ve done in the past.  Greg Lucas wrote a very helpful post as he reflected on a mother who killed her adult disabled son and then herself.  This mom had also been entrusted with her son’s care, and the hopelessness of her situation eventually overwhelmed her.

No, the trust must go deeper than a reliance our own strength or affections, because those can fail.  Thankfully, God never fails. He gave us our Paul with every intention of making His name great in every way – through Paul’s life and gifts, and through the daily help he provides to us as his parents.  If the Lord grants Paul life, eventually we’ll need to hand off his care to somebody else; I expect God will be teaching us even deeper lessons about trusting in him and his wisdom when we confront that issue.

I was impressed at how the Ramsey County Judge had full control of his courtroom.  People stand when he enters the room. Lawyers who were much older than he is addressed him as ‘Your Honor.’  When he asked for something, the attorneys supplied it without question.

But at the end of the day, this judge goes home.

We have a greater judge to ultimately trust in who never stops pursuing justice, who knows everything, and who will help us as we continue to care of our very vulnerable, almost adult son:

But the Lord sits enthroned forever;
he has established his throne for justice,
and he judges the world with righteousness;
he judges the peoples with uprightness.
The Lord is a stronghold for the oppressed,
a stronghold in times of trouble.
And those who know your name put their trust in you,
for you, O Lord, have not forsaken those who seek you. (Psalm 9:7-10, ESV)

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I posted my talk for Children Desiring God before Mother’s Day.

In my talk I mentioned that during the child dedication services, “one of my pastors makes the specific point, whether there is a disabled child being dedicated or not, that ALL children are gifts – and then he names some disabilities to make his point that these children are gifts as well.  You can’t avoid that he means all children.”

I had forgotten that every Mother’s Day, Bethlehem dedicates children to the Lord.  And Pastor Kenny did it again – even referencing that he was going to do it again!  It encourages me every single time. (My apologies for the quality of the audio)

After the children were dedicated, Pastor Bud prayed for the children and families.  I routinely record Pastor Bud when he prays. That might sound weird, but I’ve learned so much from this man about boldly coming to God with Bible-saturated prayers that I want to experience it more than once.  I hope you are encouraged by it as well.

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Note: This was first posted in 2011 for Mother’s Day. May God’s peace which ‘surpasses all understanding’ (Philippians 4:7) be with every mother today.

There are scores of women who have children of all ages who cannot speak an intelligible word because of their cognitive disabilities.  Or their children, like my son, have some language, but those children can never make a spontaneous call of deep affections for their mother.

There will be no handwritten cards, telephone calls or gifts from those children to their mothers today.

Yet, most of those children have mothers who pour their lives into them, sometimes for decades beyond what they anticipated when that little life first starting growing in their bodies.

For all of you moms in that circumstance, know that this proverb is still for you, just not yet!

Her children rise up and call her blessed.  Proverbs 31:28

Why do I believe this?

1 Then I saw a new heaven and a new earth, for the first heaven and the first earth had passed away, and the sea was no more. 2 And I saw the holy city, new Jerusalem, coming down out of heaven from God, prepared as a bride adorned for her husband. 3 And I heard a loud voice from the throne saying, “Behold, the dwelling place of God is with man. He will dwell with them, and they will be his people, and God himself will be with them as their God. 4 He will wipe away every tear from their eyes, and death shall be no more, neither shall there be mourning, nor crying, nor pain anymore, for the former things have passed away.”

5 And he who was seated on the throne said, “Behold, I am making all things new.” Also he said, “Write this down, for these words are trustworthy and true.” 6 And he said to me, “It is done! I am the Alpha and the Omega, the beginning and the end. To the thirsty I will give from the spring of the water of life without payment. 7 The one who conquers will have this heritage, and I will be his God and he will be my son.  Revelation 21:1-7

Those mothers who cling to Jesus for daily strength and as their future hope have a glorious eternity waiting for them.

Someday, I believe my son will tell me things almost too wonderful for me to comprehend about what he experienced in this present age.  And I expect one of the things he will talk about is his tender, eternal regard for the woman who cared for him without a thought about what she would receive from him in return.  On that day, he will rise and call his mother blessed!

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This was first posted on July 30, 2009 on a different blogging platform:

My wife recently enjoyed a great evening with other moms of children with disabilities.

Apparently the subject of “things people say to us” came up. 

A popular one we have all heard is “God doesn’t give you more than you can handle.”  Generally in a group of parents with disabled children, people will either start to laugh uproariously at how ridiculous this is, or begin to weep at the burden of constantly not measuring up.  Why?  Because disability is hard and we know it is way more than we can handle.

This statement is particularly hard because it sounds scriptural, sort of: 

1 Corinthians 10:13 No temptation has overtaken you that is not common to man. God is faithful, and he will not let you be tempted beyond your ability, but with the temptation he will also provide the way of escape, that you may be able to endure it.

Pastor John wrote a nice article on this text way back in 1976, and this recent blog entry by Aaron Armstrong also examines the 1 Corinthians 10:13 text. 

But even knowing this more accurate biblical context, how do you respond when somebody says that to you? 

Here are a few things I try to keep in mind:

  • They mean well.  They don’t generally get it (otherwise they wouldn’t say it), but they really want to say something helpful.  And they certainly don’t want to make things harder on us.
  • They are usually REALLY happy not to have to deal with what you have been given.  From that viewpoint, they do understand something of your situation; you probably wouldn’t have chosen to deal with it, either.
  • They are exposing their understanding of who God is, and are opening a door for you to explain who God really is.  God wants us to be entirely dependent on him (see Psalm 40 for how good this is!), because that is the kindest thing possible.  We will not learn dependence on God if we can ‘handle’ it ourselves.
  • God understands what he has given us ‘to handle’ and knows exactly how it will bring him glory and will work out for our good.
  • I know that if I respond in anger (or worse, with violence), that I have just extended the amount of time I need to deal with this statement.  And, yes, I have wanted to punch people in the nose who have said this to me.  Just not lately, because God continues to teach me his character and how good he really is to me in light of my sin.

 So, as I think about it, I am considering saying this the next time I hear that statement said to me: 

Thank you for wanting to encourage me.  In fact, God does give me more than I can handle, and I am grateful to experience his strength in my weakness.

What do you think of that?  Would that make things better or worse?

And how do you respond when people say that to you?  How would you like to respond?

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I know this video is an advertisement.  But the pictures of babies are amazing!

We must let people know right now that when they ‘see’ something they didn’t expect in their baby, like a disability, that their child is still wonderful and created for a good purpose.  They are no less beautiful just because they don’t look like the babies in these pictures.

I praise you, for I am fearfully and wonderfully made.
Wonderful are your works;
my soul knows it very well. (Psalm 139:14, ESV)

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Social media accomplished what seemed unlikely at best – it forced national media attention on the trial of a man who practiced late-term abortions in horribly barbaric ways.

Please be advised that there are very disturbing, graphic images in this video along with detailed descriptions of what happened to babies – living babies – at this abortion clinic.

Thank you to Seachange Filmmakers and Storytellers for pursuing this story.

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