Today’s Presentation…Supporting Kids and Teens Who Struggle With Anxiety

Accessibility Summit 2013Here’s my Power Point presentation for the talk I’ll be presenting later today at the 2013 Accessibility Summit at McLean Bible Church in McLean, VA…You can access our resource page on Anxiety and Spiritual Development in kids and teens by clicking on the link here

Here’s a wonderful interview with Rhonda Martin and Katie Wetherbee conducted for Inclusion Fusion  2011 on the topic of nurturing spiritual growth in kids with anxiety…

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Key MinistryOur Key Ministry website is a resource through which church staff, volunteers, family members and caregivers can register for upcoming training events, request access to our library of downloadable ministry resources, contact our staff with training or consultation requests, access the content of any or all of our three official ministry blogs, or contribute their time, talent and treasure to the expansion of God’s Kingdom through the work of Key Ministry. Check it out today!

Posted in Anxiety Disorders, Key Ministry, Training Events | Tagged , , , , , , , | 2 Comments

Joe Butler: Life with Micah, Part Two…Ability Tree becomes a reality

Joe ButlerThis past Sunday, we introduced you to Joe Butler of Ability Tree. Joe is the father of a child with autism who is being used by God to serve other families impacted by disabilities. We’re sharing Part Two of the Butler’s story today.

Joe is an Assemblies of God U.S. missionary to persons with disabilities and their families. Joe and his wife, Jennifer, founded Ability Tree as a religious nonprofit corporation in June of 2010. Joe holds a B.A. in Bible from Valley Forge Christian College and is graduating in May from California Baptist University with an M.A. in Disability Studies, with a concentration in Disability Ministry. Joe and Jen live in Northwest Arkansas with their three children, Hannah, Micah, and Clara. 

Here’s Part Two of the Butler’s story…

Through our ministry experience as interim youth pastors in 1999 to full-time vocational pastors, starting in 2004 and continuing today, my wife Jen and I noticed that families of children with disabilities were a missing piece in the body of Christ in the majority of churches across the country. In order to connect with these families we had to go where they were, in the community, not the church. With the hope of building a support network for these families, which includes connecting them to a local, accessible church.

After much prayer and confirmation, both Jen and I sensed that it was our life mission to reach out to other families like our own.  In August of 2008, we took a step of faith to come alongside these families through mission work in the United States. We started traveling around the country, sharing a message of inclusion with the church, helping churches to become more accessible in their place (facility), people, and programs.

In October of 2009, at a special needs conference in Wisconsin, my wife and I sat next to a pastor and his wife from Northwest Arkansas. We soon found out that we both had children with special needs. After sharing our stories with one another, he invited our family to come to his church to share our mission. We flew out and spoke the weekend before Thanksgiving. That morning, I shared something I had never shared before, a dream of launching a special needs outreach center in Northwest Arkansas that would reach out to families impacted by disability around the country. Shortly after we arrived back home, I shared the idea with my pastor in New Jersey and with some other close friends of mine. The next day, the pastor from Arkansas called, and I shared with him that I think God is directing us to move down to Arkansas. Ironically, he called to tell me the same exact thing! Nine months later, we were living in Northwest Arkansas and the dream of a special needs outreach center was a reality.

Ability TreeIn June of 2010 we founded Ability Tree as a religious nonprofit corporation in the state of Arkansas. The mission of Ability Tree is to reach out to families impacted by disability through recreation, education, support, and training (R.E.S.T.), we aim to partner with individuals and organizations to raise awareness and build support networks to strengthen and grow able families. We envision individuals and families, living with special needs, being accepted and supported in their local community, enjoying healthy relationships in their schools, workplaces, and churches.

One of the first individuals we met in Northwest Arkansas, was Josh Allen, of Allens Inc. Less than a year after we moved to NWA, Allens gave us a space, in downtown Siloam Springs, for the first Ability Tree Center which would be a place of R.E.S.T. for families impacted by special needs as well as a place where volunteers could learn how to interact with children with disabilities and their families through a variety of programming. School-aged children with special needs and their siblings can enjoy after school, art, and recreation programs, while parents and can receive support and resources to help strengthen their family. Businesses and organizations, like the church, can also receive special needs consulting and gain access to a library of resources.

In New Jersey, we operate a 5-day, overnight Summer Camp, called the Ability Camp, as well as a 2-week Summer Day Camp, free family-friendly community events, and weekend respite programs for children with special needs and their siblings. Currently we have offices and programming in Arkansas, Pennsylvania and New Jersey with the long term goal of having Ability Tree Centers in Main Street U.S.A. towns across the country.

The vision of Ability Tree is big. It’s my life mission, and will take at least a  lifetime to see fulfilled. We have already seen glimpses of the vision God placed in our hearts. Listen to what one of our volunteer families wrote recently…

Ability Tree is a place where my family and I have felt like we can make a difference for the individuals and families affected by disabilities. It occurred to me one day what a gift and responsibility this is for us all, not just for these specific families. Ability Tree strives to provide and strengthen community for these individuals and families, so Ability Tree is trying to reach us all.

The mom of one of our families of a child with special needs recently shared…

They [Ability Tree] have become very special to our family as we are impacted by special needs! The services, comfort, and happiness they provide to children are beyond words! My child finally has a place to go where he is not the child everyone pics on. He is accepted and that means the world to me. They have introduced us to other parents and provide a MUCH needed support group in our area! The Christian based foundation is truly a gift from GOD along with all of the amazing volunteers that give of their time.

The satisfaction of knowing God is working through Ability Tree is amazing to me!  It wasn’t long ago that I was asking God, “Why did you allow this to happen to my son”? My perspective on life has changed over the past 12 years, I would say I see more clearly what really matters and where real value lies. I thank God for Micah and who He created him to be! Being around other individuals and families living with special needs everyday, reminds me to live in the now, and not get caught up in the worries and cares of this world. I am thankful for that.

Butler familyThis past December, Micah turned 12. He is walking, talking in complete sentences, and becoming more independent each day. He’s also pestering his sisters like any good brother would do. Most importantly, he absolutely loves God, life and people. Micah is the heartbeat of Ability Tree. We are currently in a capital campaign called Project Grow to finish phase two of the Siloam Springs Ability Tree Center, which will turn an old theatre into a Recreation Center complete with indoor basketball court, soccer and whiffle ball fields. Please pray that God will provide the needed funds to carry out this part of the vision. I would love for you to follow our story, and to learn about your story. You can find us on the web at abilitytree.org, and on social media at facebook.com/abilitytreeinc and on Twitter at @abilitytree.

On a mission,

Joe

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Ability Tree reaches out to families impacted by disability through recreation, education, support and training (R.E.S.T.). We aim to partner with individuals and organizations to raise awareness and build support networks to strengthen and grow able families.

The Ability Camp allows people with intellectual and/or physical disabilities to take part in various camp-style activities that they may not be able to participate in otherwise, and gives caregivers a 5-day respite. Watch this video to see what the Ability Camp is all about.

Posted in Advocacy, Autism, Families, Hidden Disabilities, Inclusion, Resources, Stories | Tagged , , , , , , , , , | Leave a comment

Guest Blogger Joe Butler…Life With Micah

Butler familyIn celebration of Autism Awareness Month, we plan to introduce our readers to several fathers of children with autism who were led to serve families impacted by disabilities because of their experiences. First up today is Joe Butler of Ability Tree.

Joe is an Assemblies of God U.S. missionary to persons with disabilities and their families. Joe and his wife, Jennifer, founded Ability Tree as a religious nonprofit corporation in June of 2010. Joe holds a B.A. in Bible from Valley Forge Christian College and is graduating in May from California Baptist University with an M.A. in Disability Studies, with a concentration in Disability Ministry. Joe and Jen live in Northwest Arkansas with their three children, Hannah, Micah, and Clara. Here’s Part One of his family’s story. We’ll share Part Two this coming Tuesday.

December 29th, 2000, was the day Micah was born, and the day that forever changed the direction of our lives. Two days earlier, we had just sold our house in New Jersey and moved onto a Christian college campus in eastern Pennsylvania to pursue my degree in pastoral ministry. I wasn’t sure what the future held, but I was sure we were heading in the right direction.

I started taking classes full-time and working two part-time jobs during the semester and full-time during the Summer. My wife, Jen, had the full-time job of caring for our two year old daughter Hannah, and a newborn. From day one, Micah had a difficult time eating and sleeping. At his three month old check-up, we were already asking questions about his behavior and development. At nine months old, Micah was diagnosed with developmental delays. Which basically meant that he wasn’t achieving typical developmental milestones for his age.

In the Fall of 2001, Micah started receiving early intervention. Physical, occupational, and speech therapists frequented the college campus three days a week while the other days were filled with trips to Children’s Hospital of Pennsylvania for additional therapies and check-ups. We were doing everything we could do for Micah. Oftentimes, as parents, we felt overwhelmed and out of control. During those times we just did what comes naturally as parents, we continued to love and get to know our child.

Wednesday, May 7th, 2003, is a day, as a dad, I’ll never forget. We went to our church’s midweek service that night. After service, Jen picked up Micah from the nursery and brought him to me. I sat him on my lap, facing me, while I was finishing up a conversation. I felt him leaning back and I said, “Micah, sit up.” As I looked at him and said it again, I noticed that his eyes were starting to roll back in his head and he was starting to shake. Within minutes he was convulsing uncontrollably. I remember carrying him to the foyer of the church and calling for help. Two nurses, who attended our church, were there that night and cared for Micah while we waited for the paramedics to arrive. They took Micah by ambulance to the nearest hospital where they sedated him some 45 minutes later to stop the seizure. Once he was sedated they transferred him to a children’s hospital for further tests and scans.

Jen went with Micah in the ambulance on the initial trip as well as during the transfer. I had to follow in our vehicle. The hospital’s policy was that only one parent could stay overnight in the room. Jen stayed and I went back to our college apartment. I still have the picture of my son in my mind from that night right before I left. He was out cold in a hospital crib with tubes and monitors connected all over his little two year old body. If I could have taken his place, I would have.

Our oldest daughter Hannah, who was five at the time, and witnessed Micah’s seizure, spent the night at a friend’s house that night to keep her mind off of the situation. I went back to our college apartment and fell onto our bed. I remember crying out, “Why is this happening?” That night as I stared up at the ceiling, God reminded me that children are a gift from Him, and that He knew Micah before He formed him in Jen’s womb. He assured me in my spirit that He had a plan for Micah’s life and that He was in control.

I think God was preparing me for the report I was about to hear from the doctors. The neurologists said there were “abnormalities” in Micah’s brain, “that his white and grey matter were thinning.” Bottom line, they weren’t sure if Micah would walk, talk in complete sentences, or be independent someday. Don’t get me wrong, I was thankful for the diligence and care that the doctors gave Micah, but there just wasn’t much hope in their message. He was diagnosed with having cerebral palsy (and later with autism), a result, most likely, of a lack of oxygen during the first trimester of Jen’s pregnancy. Reality began to set in. This was more than a developmental delay.

On Tuesday, July 1, 2003, our third child Clara was born, six weeks early. Jen had a gallbladder attack, the previous Sunday morning and was rushed to the hospital. Clara spent nine days in the neonatology intensive care unit (NICU) before coming home. Micah loved his new little sister and she became a motivator for him. He didn’t want her to surpass him in any milestones. Micah continued to work hard, through a variety of therapies, to accomplish what most children learn naturally, like walking, talking, and fine motor skills.

I graduated in May of 2004, and took a full-time associate pastor position in southern New Jersey. It was there that Micah learned to walk independently at the age of four. The size of the church was fairly large and there were several other families with children with special needs. Because of my role as associate pastor and because my wife and I were the parents of a child with special needs, other families looked to us for counsel and direction.

We pastored at two churches over the next four years. During that time we connected with more families of children with special needs and helped include them into the life of the church. The more we learned about special needs ministry, the more we learned that the majority of churches weren’t equipped to include families with special needs. Both Jen and I sensed that it was our life mission to reach out to other families like our own.

Fast forward to the present day. Hannah is 14, Micah is 12, and Clara is 9. Life with Micah has taught our family very valuable lessons-to enjoy the everyday moments and happenings in life. Don’t take anything for granted. Notice the delivery trucks on your way to work and say hello to the greeter at Walmart. Get excited when you see a dog or cat and even more excited when you see a family member. Say, “I love you” several times a day. Don’t be afraid to cry, or make a mistake, or say, “you’re sorry.” Live life to the fullest.

To be continued… On Tuesday, Joe will share the the story of what his family is doing through a nonprofit organization they founded several years ago. 

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Ability Tree reaches out to families impacted by disability through recreation, education, support and training (R.E.S.T.). We aim to partner with individuals and organizations to raise awareness and build support networks to strengthen and grow able families.

The Ability Camp allows people with intellectual and/or physical disabilities to take part in various camp-style activities that they may not be able to participate in otherwise, and gives caregivers a 5-day respite. Watch this video to see what the Ability Camp is all about.

Posted in Advocacy, Autism, Families, Inclusion, Key Ministry, Resources, Stories | Tagged , , , , , , , , | Leave a comment

Our kids (and families) aren’t defined by a diagnosis…

shutterstock_146517839I had a conversation last year with a parent  after their child received a diagnosis of Asperger’s Disorder…they gave me permission to share my part of our discussion with our blog readers. While this conversation pertained to a child with Asperger’s, the same principles apply to a full range of mental health or developmental disorder diagnoses. 

Your child is not defined by their diagnosis. They’re the same kid they were when they got up this morning, with the same strengths, weaknesses, gifts and talents. As Christians, we’re defined by who we are in Christ. Your child’s diagnosis is not their identity.

As a clinician, a diagnosis is a mental model we use as a framework for organizing our observations about a child we’re treating…a tool to help us consider what we might be able to do to help. Sometimes the label helps us to qualify a child for educational or rehabilitative services, or predict responses to specific treatment options. One of the comments I share with residents and fellows who come through our practice pertaining to diagnosis is…“I don’t care what you call it as long as you know what to do about it.” What matters is that the people caring for your child understand them and meet their needs.

600817_10200479396001791_905419060_nYou also need to keep in mind that psychiatric diagnoses are very subjective and open to interpretation…I was at a remarkable lecture last night with a clinician who will be training psychiatrists, psychologists and counselors to use the DSM-5 when it comes out in a couple of months. Statistically speaking, two psychiatrists evaluating the same patient are FAR more likely to disagree than agree on the patient’s diagnosis. Your child’s diagnosis is not necessarily carved in stone.

I understand that it can be very hard as a parent to have a concrete reminder on a piece of paper that your child is “different.” I get that the mention of Asperger’s churns up all the fears you experienced when your child was 2 1/2 and you first suspected that their social development wasn’t progressing as expected. But the help recommended for your child certainly seems appropriate…they could certainly benefit from developing a more positive (and realistic) self-image and from learning tools and skills to help them to manage their emotions more effectively.

Most importantly, there are no accidents. God had a plan for your child’s life this morning, and I don’t think God’s plans for your child are contingent upon whether or not the psychologist thinks they meet the criteria for Asperger’s. God probably has a plan to use you and your experiences to help other parents and families going through similar experiences. For as much as we love our kids, God loves them infinitely more. God has a plan for them…and His plan isn’t going to be thwarted by a diagnosis.

Updated July 5, 2014

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KM Logo UpdatedKey Ministry has assembled resources to help churches more effectively minister to children and adults with ADHD, anxiety disorders, Asperger’s Disorder, Bipolar Disorder, depression and trauma. Please share our resources with any pastors, church staff, volunteers or families looking to learn more about the influence these conditions can exert upon spiritual development in kids, and what churches can do to help!

 

Posted in Autism, Families, Hidden Disabilities, Mental Health | Tagged , , , , , | 3 Comments

Autism Awareness Month…What about the siblings?

Swindoll grandkidsI received an e-mail last week from one of our former Board members who had recently spent time with a young adult sibling of a child who had been served for a number of years through the special needs ministry of her church. Her impression was that this young adult was continuing to struggle with the lingering effects of the dynamics in a loving Christian family impacted by a child with special needs, and her intuition is that there are lots of teens and young adults in the same boat who could very much benefit from the care and support available through a local church. Her quote…

“Not that you all need more to add to your already full plate, but would love at some point to see the ministry address this.”

imagesIn honor of Autism Awareness Month, I thought it would be appropriate to share a few resources focusing on siblings of kids with special needs, along with a wonderful resource from the Key Ministry website.

Gillian Marchenko is running a respite ministry in the church in Chicago where her husband serves as senior pastor…Here’s a link to an article she wrote last May in Chicago Parent magazine…Siblings in a Special Needs Family.

Here’s a featured post from Jolene Philo’s blogSiblings of Kids With Special Needs: Do Their Lives Change? 

Here’s some good advice from our friend and colleague Barb Dittrich for parenting siblings of kids with disabilities…Equal, but Different.

And finally, here’s a fabulous video Katie Wetherbee shot for Inclusion Fusion 2011 (available on our website) with Cody Thompson, Ashley Dane, and Austin Dane (siblings of Jonathan…Colleen Swindoll-Thompson’s son, Chuck Swindoll’s grandson) about their experience as siblings of a child with autism for Inclusion Fusion 2011…

Do you have great resources for those seeking to serve siblings of kids with special needs? Please feel free to post helpful resources in the comments section below.

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Accessibility Summit 2013Our Key Ministry team will be hitting the road to be part of the 2013 Accessibility Summit, hosted by McLean Bible Church in suburban Washington D.C. on April 19th-20th. This year’s Summit features Emily Colson (daughter of Chuck) As an artist, author, and speaker, Emily is passionate about inspiring others to persevere through their challenges and appreciate life’s gifts. In her book Dancing with Max, she and her late father share the struggle and beauty of life with Max, Emily’s son with autism.

For more on our Key Ministry presentations, click here. For more information on the Summit and registration, click on the Summit logo to the right.

Posted in Autism, Families, Inclusion Fusion, Key Ministry, Resources | Tagged , , , , , , , , , , , | 1 Comment

Mental illness can kill…even in the best of families

imagesI’ve never personally met Rick Warren or his wife…although I was very flattered when I learned he was “following” me on Twitter, but I’d ask all those who follow our blog to keep Rick, his wife Kay, and those close to his family in your prayers. Rick and his wife shared this prayer request with the people of Saddleback Church earlier today…On behalf of our Board, staff and volunteers at Key Ministry, we would pray the Warren family would experience God’s comfort and presence during this difficult time, and that God will use Matthew and the circumstances around his death for good, bringing God greater honor and glory and for the expansion of His Kingdom.

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We live in a broken world with broken bodies and broken minds. I come across families all the time in my practice who live every day seeking to honor God who pray every day for their children struggling with some type of mental illness that they would experience healing and an inner peace. Sometimes God doesn’t answer their prayers in the way that we would desire or expect. I can’t imagine how any kid could have more godly parents than Rick and Kay Warren. There aren’t many families alive that have done more to advance the Gospel than the Warren’s. It’s reasonable to assume that they prayed continually for their son and did everything they possibly could to relieve his distress since the onset of his mental illness.

What I find reassuring…and highly motivating in this tragic story…is that by Rick’s account above, Matthew had come to know and believe in Jesus, and his family and friends can be assured today in the midst of their despair that Matthew is finally at peace and living in the presence of his Heavenly Father who loves him infinitely more than his earthly family above. About the only thing I can think of that would be more difficult than what the Warren family experienced this morning would be losing a child to suicide without the assurance that they’d be living forever in the presence of Jesus.

Several observations I’d like to share…

  • Growing up in a loving family of great faith or coming to a personal faith in Jesus Christ is no guarantee of being spared of the pain and suffering of mental illness while living in a fallen world.
  • As a physician practicing child and adolescent psychiatry, I fully appreciate the seriousness of mental illness. An argument can be made that outside of trauma surgeons and emergency room physicians, my medical specialty probably sees more teens and young adults in life and death situations than any other. According to the Centers for Disease Control, suicide is the third leading cause of death in the U.S. among persons ages 10-24, and the second leading cause of death (behind only motor vehicle accidents) in 25-34 year olds. Among 15-24 year olds, suicide is three times more common than death from cancer. Kids and young adults die from mental illness, and sometimes the best psychiatrists and therapists can’t do much about it.
  • Finally, it’s absolutely unacceptable to me that there are far too many kids and far too many families struggling with potentially lethal mental illnesses who haven’t had the opportunity to learn about Jesus and come to faith in Him or be a part of a family of faith (like Saddleback). One way for those of us in the church…especially those of us in the disability ministry movement…to honor the memory of Matthew Warren would be to radically expand our efforts to reach out to and share the Gospel with kids, teens and young adults impacted by mental illness and their families.

“Do not let your hearts be troubled. You believe in God; believe also in me. My Father’s house has many rooms; if that were not so, would I have told you that I am going there to prepare a place for you? And if I go and prepare a place for you, I will come back and take you to be with me that you also may be where I am.  You know the way to the place where I am going.”

John 14:1-4 (NIV)

Photo from Christian Post

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Key Ministry’s mission is to help churches reach families affected by disability by providing FREE resources to pastors, volunteers, and individuals who wish to create an inclusive ministry environment. We have designed our Key Catalog to create fun opportunities for our ministry supporters to join in our mission through supporting a variety of gift options. Click here to check it out! For a sixty second summary of what Key Ministry does, watch the video below…

 

Posted in Families, Key Ministry, Mental Health | Tagged , , , , , , , , , | 9 Comments

What would JEREMIAH do? Teaching at Martindale Christian Fellowship…

Martindale

I’m honored to be invited back to Martindale Christian Fellowship Church in Canton, Ohio by Senior Pastor Steve Manko and his team to teach at their morning worship on Sunday, May 5th. My topic will be…What Would Jeremiah Do?…Representing Christ Well Amidst a Culture in Freefall.

JeremiahJeremiah was called by God to serve as a prophet and deliver a very difficult message to the leaders of the Jewish people during a time when pagan worship, sexual immorality and child sacrifice were officially sanctioned by the leaders of the nation. His ministry spanned the time from the reign of King Josiah, Judah’s last “good king” through the siege and destruction of Jerusalem by King Nebuchadnezzar and the Babylonian army, an attempt by a remnant of Judah to flee to Egypt, and the beginning of the Babylonian captivity. Jeremiah experienced significant persecution and discomfort because he was faithful to his call to “speak truth to power” and communicated a message from God in direct opposition to the culture of the day.

We’ll look to Jeremiah’s life for insight and understanding as to how God wants His servants to carry themselves during a time when remaining faithful to the teachings of Scripture is decidedly uncool.

I’d like to take this opportunity to invite as many of our followers as possible to join me at Martindale Christian Fellowship in Canton at 10:30 AM on Sunday, May 5th. Driving directions to the church can be obtained here. Hope to see you there!

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Key Ministry’s mission is to help churches reach families affected by disability by providing FREE resources to pastors, volunteers, and individuals who wish to create an inclusive ministry environment. We have designed our Key Catalog to create fun opportunities for our ministry supporters to join in our mission through supporting a variety of gift options. Click here to check it out! For a sixty second summary of what Key Ministry does, watch the video below…

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Chuck Swindoll talks about autism…

DSCN7741Among the free resources available on the Key Ministry website is a two-part interview Katie Wetherbee conducted with Chuck Swindoll and his daughter Colleen for Inclusion Fusion 2011. During the interview Chuck and Colleen discuss their experiences at length of living with Jonathan, Colleen’s youngest son who has been diagnosed with autism.

Chuck spoke at length about the impact of Jonathan’s disability on their family, how his presence in the family has been a blessing, and how Jonathan has helped him become more effective in his ministry to people with disabilities. Chuck also addresses the question of how seminaries can better prepare pastors to minister to families impacted by disability. Colleen has some great insights for leaders in the church on how to communicate sensitively with families of children with disabilities. Chuck and Colleen also spoke of the impact of Jonathan’s disabilities on the other kids in their family.

Chuck has been among the most influential Bible teachers and Christian leaders of the past half century. His teaching is broadcast on over 2,000 radio stations around the world in seven different languages. He is the author of over seventy titles, including The Church Awakening, Embraced by the Spirit and The Grace Awakening.

Chuck currently serves as the Chancellor of Dallas Theological Seminary, after having served as President of the seminary from 1994-2001. He continues to serve as the founding pastor of Stonebriar Community Church in Frisco, Texas. Stonebriar is home to a highly regarded special needs ministry.

World Autism Awareness DayChuck and his team at Insight For Living have had a longstanding interest in ministry to families of kids with special needs. Members of our Key Ministry team have had many conversations with IFL staff over the past six or seven years around areas where our organizations might collaborate. Stonebriar Church had published one of the earliest comprehensive guides to church-based special needs ministry (no longer in print). Chuck did a series of radio broadcasts years ago with his daughter, Colleen about the impact of his grandson’s symptoms of autism on their family.

Colleen Swindoll-Thompson serves as the Director of Special Needs Ministry at Insight for Living, where she regularly blogs, maintains an active presence on Facebook through the “Special Needs Ministry” page, personally ministers to parents and families worldwide struggling to raise kids with disabilities, and has assembled an array of resources for parents of kids with special needs.

Here’s Part One and Part Two of Katie’s interview with Chuck and Colleen…

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Key MinistryOur Key Ministry website is a resource through which church staff, volunteers, family members and caregivers can register for upcoming training events, request access to our library of downloadable ministry resources, contact our staff with training or consultation requests, access the content of any or all of our three official ministry blogs, or contribute their time, talent and treasure to the expansion of God’s Kingdom through the work of Key Ministry. Check it out today!

Posted in Advocacy, Autism, Families, Hidden Disabilities, Inclusion Fusion, Key Ministry, Leadership, Stories | Tagged , , , , , , , , , , , | 4 Comments

Commentary…CDC reports 20% of high school boys diagnosed with ADHD

Rates of ADHD diagnosisThe New York Times is reporting that the most recent U.S. Centers for Disease Control study of children’s health issues shows that 11% of U.S. children ages 4 and above have been diagnosed at some point in their lives with ADHD. The study also reports that 15% of boys have been diagnosed with ADHD, and that nearly 20% of high school boys (along with 10% of high school girls) have received an ADHD diagnosis and one in every ten high school boys currently takes medication for ADHD. The data was compiled by reporters from the Times from raw data on the CDC website from the 2011-12 Survey of Children’s Health Issues…a phone survey of 95,000+ U.S. households, with a minimum of 1,800 surveys from each U.S. state. Here’s a link to the full article in today’s New York Times…I would encourage you to read the article for the comments of prominent physicians quoted in the piece. Here’s my two cents…

  • Assuming the data are accurate, we have a serious societal problem if 20% of our high school boys have a condition that by definition requires functional impairment in at least two settings and “clear evidence of interference with developmentally appropriate social, academic or occupational functioning.” We need to consider the possibility that the demands and expectations of the environments where our kids and teens spend much of the time are a big part of the problem and question whether we need to rethink our expectations for academic productivity and the design of the learning environments where our kids spend much of their day.
  • I’d hypothesize that too many kids are getting a diagnosis of ADHD without an appropriately thorough assessment from a physician or other professional with the proper training and qualifications to diagnose. One immediate observation I made when reviewing the graphic from the article (above) is that many of the states where the prevalence of ADHD is highest are states where the shortage of child psychiatrists is most acute. If I had one takeaway point for parents from this discussion, I’d encourage them to make sure that whoever they take their child to for assessment or treatment of ADHD takes the time to do a comprehensive assessment including separate interviews with the parent and child, input from teachers and other adults from outside the family involved in the child’s life and a thorough review of the child’s educational records, including report cards and standardized testing results. Some of this may be a byproduct of physicians (the majority of whom are now employed by large clinics and healthcare organizations) pressured to see too many patients in too short a period of time.
  • I’m a big proponent of free speech, but I wouldn’t have any problem with Congress passing a law to prohibit “direct-to-consumer” advertising of prescription drugs to the general public. Back in the day when I spent much of my time involved in physician education it became obvious to me that for all too many doctors, the path of least resistance was to give patients what they asked for, especially if their experience or communication skills made it difficult for them to explain concisely why a specific product or treatment may not be in the patient’s best interest.
  • We need to examine the possibility that medication is being used as a substitute for effective psychosocial treatments in our publicly-funded mental health centers, or as a replacement for appropriate assessment and remedial education services in public schools in impoverished areas. Rates of medication usage are significantly higher among kids covered under Medicaid compared to private insurance.   While some of this discrepancy may be due to genetic loading (unplanned pregnancy rates are higher among persons with ADHD, divorce rates among parents of kids with ADHD are double that of families in the general population up to age 8), medication may be the only option in situations when high quality counseling or effective educational interventions are unavailable.
  • Finally, I wonder if the explosion of technology available to kids may be fueling our ADHD epidemic? I did a brief Medline search looking for high-quality studies demonstrating an association…the available data is muddled and doesn’t adequately control for kids who seek out technology as an escape from academic frustration or because they already have ADHD and computer games provide gratification mediated through dopamine reward circuits in their brains. Experientially, I’ve found that I crave more new information and have a shorter attention span after spending too much time with social media. We do need well-designed studies to look at the impact of texting, social media, smartphones and video games on traits associated with ADHD.

Those are my thoughts…What do you think?

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ADHD Series LogoCheck out Key Ministry’s page on ADHD and Spiritual Development! The page features links to an extensive blog series, expert tips on teaching kids with ADHD from Karen Sunderhaft, links to a video featuring Dr. Russell Barkley explain brain mechanisms in children and adults with ADHD, and links to the American Academy of Child and Adolescent Psychiatry’s Resource Center on ADHD. Feel free to share the links with church staff, volunteers, friends and family members.

Posted in ADHD, Controversies, Families, Key Ministry, Mental Health | Tagged , , , , , , , , , , | 3 Comments

Autism Awareness Month…New blog series and more!

AS_12-LIUB-Twitter-IconApril 1st marks the beginning of Autism Awareness month…as we have in previous years on the blog, we’ll use the blog to draw attention to autism-related topics.

Last year’s featured series for April examined the impact of Asperger’s Disorder on spiritual development in children and teens. This year, our focus will be twofold.

First, I’ll be doing a miniseries on The Evidence for Complimentary and Alternative Treatments for Kids With Autism Spectrum Disorders.

Throughout April, we’ll be featuring guest blogs from several fathers of children with autism. We’ll also be featuring resources on the Key Ministry website to help churches more effectively support families of kids with autism spectrum disorders.

Here’s a little preview…While not yet posted in the Inclusion Fusion video library, here’s Dr. Cara Daily’s presentation from Inclusion Fusion 2012, Do I Have to Have Surgery to Open My Heart to Jesus?, in which she discusses strategies for presenting the Gospel to children with autism spectrum disorders

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Accessibility Summit 2013Our Key Ministry team will be hitting the road to be part of the 2013 Accessibility Summit, hosted by McLean Bible Church in suburban Washington D.C. on April 19th-20th. This year’s Summit features Emily Colson (daughter of Chuck) As an artist, author, and speaker, Emily is passionate about inspiring others to persevere through their challenges and appreciate life’s gifts. In her book Dancing with Max, she and her late father share the struggle and beauty of life with Max, Emily’s son with autism.

For more on our Key Ministry presentations, click here. For more information on the Summit and registration, click on the Summit logo to the right.

Posted in Autism, Key Ministry, Resources, Spiritual Development | Tagged , , , , , , , , | Leave a comment