Now, congratulations to the winners of a copy of Lynn’s book, His Revolutionary Love. The winning commenters are:

Godchozn and Angela Sladovnik.

Please email your shipping address to me at: info@kellylangston.com. Thank you!

That creates a common situation where there is a neurotypical daughter, a sibling of an autistic brother. My own family is an example of this situation.

Six Ways to Build a Bridge to Your Girl’s Heart

Boys … how are they typically described? Rambunctious, loud, messy, insensitive. Then there are our girls. So often they are compassionate, strong, capable, even at times the backbone and heartbeat of our families.

Unlike you, I do not have a child who has autism, but my first born son did come with his own unique packaging. This has put my two daughters in places where they have had to step up and mature faster than I would have desired. Yes, God has used this to make them strong.  As their mom, though, I want to be aware of my girls needs. They need to be told they are beautiful. They need to be reminded consistently that they are loved. Like a plant in the hot Carolina summer sun, they need to be poured into on a daily basis so that they flourish and blossom.

This is no easy task, especially when we have another child who needs are much more apparent. Yet, friend, we cannot mistake the quiet stability of our girls as their lack of need. They need us to build a bridge to their heart; connecting our heart to theirs.

Here are six ways that you can build a bridge to your daughter’s heart:

1. Be informed.

   Be informed about what is happening in your girl’s world. What things make her anxious? A friendship? You know many times relationships with girls can be more complicated than boys! For over ten years I have been mentoring, speaking and writing to teen girls. Girls carry a lot of anxiety. They need to know being needy isn’t bad; that’s where God comes in! Much anxiety can be alleviated by simply by talking. Know your girl’s heart. When you do this, you say to your girl, “I care enough about you to learn your world.” 

2. Be approachable.
   

   Often what our girls need most from us is a safe place to talk. Recently, my daughter Madi was telling me about a friendship problem. I asked her, “Would you like me to just listen or do you want advice?” She said, “Just listen.”

   An approachable parent responds instead of reacts. We should be thermostats instead of thermometers. Thermometers tell us the temperature of the house, a thermostat sets it. By responding instead of reacting we are setting the temperature of a safe place to be yourself and be heard. 

3. Be available.
   

   Slowing down is important so we can be there for our children. Different kids will be more vulnerable and open at different times. Think over your life and your schedule. How can you arrange things so that you can be available to your daughter to hear about her world, her heart and the things she is going through in her mind?
   

4. Be vulnerable.

   Pouring into teen girls has been one of the Lord’s greatest gifts to me. These girls would say, “I wish I could talk to my mom like I can talk to you.” Or, “I wish my mom would tell me things about when she was growing up.” It is important to share with our girls the things we struggled with when we were their age. Of course, we need to do so as the Holy Spirit directs us and as it appropriate for their age, but our kids need to hear from us our struggles, our victories and our falls. When your child is struggling have you shared some of your stories with her? Does your child realize that you, too, struggle? 

5. Be her discipler.
   This is our chance to share with our girls what the Lord has done for us by going through His word with them. This can take place in two ways: informally and formally. Informally, I look for opportunities to tell my kids what Jesus is doing in my life. In the car, going for a walk or having a snack, I share how the Word helps solve problems.

   Formally, when my kids are eating their breakfast, I read God’s Word to them. I also have a small group for my youngest daughter and five of her ninth grade friends. Every other week we get together to do a Bible study and learn more about Jesus and his love for them. By following a formal format, I am reassured that we will have a pre-set time to read and study His Word together. 

6. Be willing to speak truth. 

   When your girl is looking in the mirror and lamenting over that zit on her forehead, remind her that Jesus says in Psalm 45:11: “The king is enthralled by your beauty.” When she feels rejected because everyone else has a boyfriend and she doesn’t, speak that truth “I am my lover’s and he is mine!” (Song of Solomon 2:16). When she wishes for a bigger chest and a smaller waist, speak to her, “You are altogether beautiful my darling and there is no blemish in you.” Your girl needs to know that the love she needs can never come from a guy – they just don’t have what it take; but Jesus has all she needs and then some!  

Remember:

You are the vessel, my friend, that the Lord can use pour the truth of unconditional love into your girl. Fill up and then pour out!

Lynn Cowell is a speaker and writer with Proverbs 31 Ministries. She lives in North Carolina with her husband of 24 years and her three teenage children. She has just released of her first book “His Revolutionary Love: Jesus’ Radical Pursuit of You”; a study for young women. She loves sushi, well worn sweatshirts and anything that combines chocolate and peanut butter. You can access free resources for you and your girl at www.LynnCowell.com.

I am very pleased to have Jaime Rafferty, author of Finding the Right Piece: Using Laughter and Faith in the Puzzle of Life (Crossbooks Publishing), share this precious post today about letting go of our own dreams for our children only to discover the thrilling life that God intends for them.

Now for Jaime’s post:

Could the first part of the title of this post possibly be any more depressing?  I might as well have called it, “A Visit from the Grim Reaper”.

Growing up, I don’t really recall the desire to be a mom. It was because I wasn’t sure I would be any good at it… and low and behold, some days I am not. (Smiles.) Poor Beau and Brynna, my children, but thank God for a wonderful Daddy…YOU GO PAUL!

Although I didn’t have this longing, the elation I had when I found out we were pregnant with our first child, Beau (as well as the 2nd time with Brynn), took away any doubt about my reservations of becoming a parent.

If I am honest, when we have children (by birth or adoption), we sometimes impress our own dreams — dreams that have gone by or been lost — upon them.  If we are “lucky”, they may carry the passion for something that we did in our youth, or perhaps go in a direction that amazes us and surpasses anything we could have dreamed up for them or ourselves.

For some parents, though, it seems that some of our dreams go unfulfilled in our children. I know that must sound selfish, right?  Please bear with me.

When Beau began showing signs of autism, both Paul and I had more emotions than we knew what to do with.  When he was diagnosed, although it was a relief to put a name to his perplexing behavior, we realized that many of the dreams we had for our son may never come to fruition.

Some thoughts that haunted us were:

Will he fit in with other kids? 

Will he have trouble in school?

Will he ever play sports?

Will he have the ability to learn?

Will he ever be potty trained?

Will he graduate from high school?

Will he be able to go to college?

Will he get married?

Will he ever be able to work full-time?

Will he be able to live on his own?

Who would take care of him if something should happen to us?

Some of those questions may seem petty, however they were very real feelings for us. Perhaps a dream that you once had was not in God’s plan for your life, and if so, then you completely understand what I am saying.

I have had the absolute honor of speaking with a young mom, Whitney.  She and her husband recently had their third child (another BOY!!). This joy has been somewhat clouded by issues they are facing with their oldest son. When we spoke for the first time, our stories were eerily similar…tantrums, peculiar behaviors/quirks, lack of social skills and so on. Although her son did not have a diagnosis, I was pretty sure by her description that our sons shared the same fate: autism. This was confirmed when he received a formal diagnosis. I wish autism on no family!  Paul and I know the struggles and heartache it can bring.

For me, I honestly try to find the blessings. As Beau’s mom, looking for the unseen blessing in autism helps me cope with the reality of dreams unrealized: often times societal dreams parents may have for kids.

I know that were it not for autism, I may not have the love and compassion for many other things. It is from our experience with Beau that I can say that.

Paul and I truly have seen LOVE, nurturing and so much more out of that diagnosis.

This love comes from the people that have worked with Beau, from Beau himself, from our families, and especially our sweet girl Brynn. (Smiles.) Have we seen the stares, heard the ugly comments and felt a lack of understanding?  Yep, we’ve seen all of that.  However the good has far outweighed the bad!

When Whitney told me of their diagnosis, though I was saddened, I knew it wasn’t a death sentence.  The news could be so much worse. It took me back to the way Paul and I felt so many years before. Whitney had a right to grieve this news. That’s her baby!! We, too, had our share of feelings of anger and confusion (and sometimes we still do)!

It’s almost like we mourned the thought of a “normal” existence for Beau, and for us, too.  The thing, at least for right now, is that Beau’s existence is completely normal to him. He is a 10 year old, often blissfully happy, fun-loving little boy.

We are the ones with crazy dreams for him. (Smiles.) He hates sports, and it would be cruel and unusual punishment for us to make him even try them. This summer while on vacation, Beau approached the sales rack at a Nike store and picked up a shirt he knew was made for him, it read, “You are a sports blooper

waiting to happen.”  Praise God that we can laugh over some of these thoughts now, 6 years after our diagnosis.

I don’t think I ever prayed that God would take autism away from Beau.  Paul may have, but I’m not sure.  The reason I wouldn’t is this:

We could all learn a few lessons from Beau Rafferty. 

Beau is honest (to a fault…LOL), he makes no judgements (at least he doesn’t verbalize them), he has an amazing sense of humor (WOO-HOO), and he is a WONDERFUL big brother to Brynn (and she likewise is a terrific sister!).

After seeing all those wonderful attributes,
what more could Paul and I have dreamed for our son?
Though autism wasn’t something Paul and I planned for…God did!

As I become closer to the Lord, I have seen and used many verses in our blog, in our book and in our life, but when I think of rearing our children, only ONE comes to mind.  I’m thankful because God uses this verse with Paul and I whenever things in our life, as it relates to Beau, become difficult for us to handle. Today I share this favorite, a verse loved by many:

For I know the plans I have for you,” declares the LORD,
“Plans to prosper you and not to harm you, plans to give you hope and a future. 

 – Jeremiah 29:11 

I now realize that it’s not for Paul or me to know Beau’s plan — we will leave it to the One who created Beau.

Here is a little something that blessed me whenever I am worried about Brynna or Beau: I inserted both of their names where it says “you” in Scripture: ”For I know the plans I have for you, Brynna, declares the LORD….” Talk about assurance!

This verse is often used as a reassurance for our own lives and walk with God, but I have chosen to also use it when I worry about the “lost dreams” for my kids. The verse reminds me that there is NO such thing as a lost dream!  There is a plan at work — a plan to prosper them (spiritually) and give them MORE than any earthly parent could ever dream!!!!

Just because Beau has autism, Paul and I still have the responsibility, as followers of Christ, to plant the seeds of faith through our daily living. It is up to me to know what Beau understands and what he doesn’t. It’s God who grants wisdom through understanding.

I don’t have a crystal ball and don’t need one as a child of God!  His word speaks my future when I remain in Him. His word speaks a future for my children if they remain in Him also!

It’s the death of our old dreams (without Him) that is exactly what must happen for us to get one step closer to the fulfilling life that He has in store for us!

I pray for you today: Perhaps there have been dreams that have died in your life or in the lives of your children. I insert YOUR name into Jeremiah 29:11 and let HIM reassure you.  Though trials will come, our hope lies in the overall plan for our future. When we LET him, we can live a life far more blessed and peaceful than anything we could have ever “dreamed” up. (Smiles.)

About Jaime: 

For as long as I can remember, a poem has been hanging on my refrigerator; I read it every morning before I grab my apple. It says:

“Blessed are you who stand beside us
as we enter new and untried ventures,
for our failures will be outweighed
by the times we surprise ourselves and you.”

    It is in human nature to judge a book by its cover: to underestimate those for whom we have formed preconceptions. I have learned throughout my six years of being a volunteer counselor at Special Camp for Special Kids to defy this universal truth. In an environment where everyone is viewed equally, regardless of intellect, physical ability, or emotional stability, I have matured in many ways far beyond my years. As a spokesperson for this particular camp, I preach acceptance, optimism, and the ability to look beyond the “book cover” of a child who might be physically or mentally challenged or both.

My younger brother, Jim, was diagnosed with autism at age two. I didn’t quite understand what that meant when I was younger, all I knew was that he had  “helpers” come in every day, got to take longer baths than me, and our mom would read books to him before he went to sleep years after I was reading Harry Potter on my own. I never quite understood why people would stare at the grocery store; make comments in passing at the park, or request different classrooms at school.

Our world is laden with abnormalities; who is a stranger to judge what is normal and what isn’t? My brother is one of the happiest, smartest and most carefree people I know- last time I checked those were qualities to be desired, not judged. Some refer to Jim as the “human GPS”, for he can give you directions to the middle-of-nowhere Arkansas as long as he’s been there once in his lifetime. Others call him “The Mayor” to honor his passion for social greetings.  His autism doesn’t change anything, and as he enters his sophomore year of high school, he has developed into a brilliant person. I always have and always will love my brother and see him as an equal, but the rest of the world won’t, just because his brain functions a little differently.

It wasn’t until the summer before my 8^th grade when my family discovered an environment where there was no “judging a book by its cover” theme: Special Camp for Special Kids. From that summer on, Jim and I would participate in camp for a week, me being a counselor and Jim a camper. Each counselor is paired up with a camper with special needs. Sure, it is a week where normally functioning teenagers give back and help the community, but most of the counselors know that they’re the truly fortunate ones. Special camp is merely one week, yet it has the potential to build memories that will last a lifetime. I look forward to that one week every year, and I will continue to do it far beyond high school.

Programs like Special Camp and Best Buddies have greatly influenced what occupation I wish to pursue in the future. Special Camp for Special Kids has challenged me to be the most accepting and patient person I could ever be, to ignore the stares of judgmental people and most importantly, to realize that a wheelchair or medical diagnosis doesn’t inhibit one from doing anything they set their mind to.

Broken.

That’s what it was now, broken, with an asymmetrical flutter to wings that only moments before lifted the butterfly in a dance around the church lawn. Only a few seconds ago I had stood watching sunlight reflect off of its colorful wings as it bounced across the blades of grass.

The butterfly, however, was not what had first caught my eye as I stood in line to pick up my son, Alec, from a day camp for special needs children at a local church in town.  It was the child — the boy with autism — that first captured my attention.  He was tugging on the arm of his caregiver with a brawny strength, roughly pulling her this way and that as they waited for his family to come for him.  The boy jerked the girl from spot to spot, physically unable to stand at a stillness.  The young caregiver gently pulled him back to a safer place, never losing her smile, each time he got too close to the parking lot or a passing car. She never let go of his hand.

As I watched the two in a strange dance of their own, my heart ached for the boy just as it does whenever I see a child struggling with autism. That familiar feeling rose from the pit of my stomach, the same one that I felt when I did not know how to reach my autistic son Alec in his younger years.  I will never forget how hard and long the days could be.

Lost in my memories, I was more than happy when the butterfly caught my eye. I couldn’t help but notice the tiny insect, darting from blade to blade with a seeming carelessness.  I was so entranced by its dance that I forgot the sun’s scorch on the 100 degree day.

I can only describe what happened next as a visual that still haunts me.  

As I watched this butterfly, the boy appeared from behind me, pulling his caregiver to where I was standing. In one quick swoop – and before his caregiver could stop him – his hand shot down and captured the butterfly in his clenched fist.  She pulled it free from the boy’s grasp and I watched fragile wings fall to the sidewalk. Now earthbound, the butterfly fluttered for a few moments before dying.

Isn’t it strange how something so simple can hit you so hard?  I could feel grief rising in the back of my throat, but I wasn’t sure what it was about the scene that hurt me most. Was it the brokenness of a boy who longed to touch something beautiful and carefree, only to crush the life from it?  Or was it the thought of how quickly something so lovely can die?

The vivid scene stuck with me all night. I prayed that God would help me understand why there is so much pain in the world.  I couldn’t shake the image of the butterfly’s falling wings from my mind.

The  next morning, I packed Alec’s lunch and we drove off for another day at this excellent day camp.  I parked the car and walked with my son up to the church.  I stepped onto the sidewalk right behind a little girl about 8 years old with Down’s Syndrome.  The sunlight bounced off of her golden hair as she skipped along holding her mother’s hand.  Without a care in the world, she sang a song and when I heard the words that she sang, I stopped in my tracks:

“I am a beautiful butterfly!  I am a beautiful butterfly”

With each light step, she twirled and sang this little song. A tingle ran up my spine as I realized what God was showing me.

Yes, Lord, I get it!  These handicapped children are the butterflies. They are full of beauty! Filled with grace and wonder, and even so, they are broken. But oh, how lovely and special they are to You, Lord, and how precious a gift it is to get to behold one single moment of the beauty that lives within them!

Graced.  We are graced to be touched by the beauty that exists in brokenness. There is a beauty beyond compare in brokenness. How precious it is to be a parent to one of these broken, beautiful butterflies, to be privileged to see God carry them through painful days by the strength of an encouraging smile.  To feel the loss of what might have been, the crush of overwhelming need, and the Divine Light that runs through it all and makes it worth our efforts.

Thank you, Sweet Jesus, for choosing me to love a child with a special need.

After I entered the church that morning, I noticed that each of the day campers wore a handmade name tag necklace tied with yarn.  Each child’s name was printed on a cardboard silhouette of — you guessed it – a butterfly.

Alec’s teenage camp buddy leaned down to greet my son with a high five and a smile.  Then I noticed something else. All of the counselors wore colorful shirts with the words “I am a New Creation” on the front. On the back of each shirt was the week’s Bible verse:

Therefore if anyone is in Christ, he is a new creature;
the old things passed away; behold, new things have come.

2 Corinthians 5:17

Finally, I understood!  Like the butterfly, we are all broken, but, praise God, there is great beauty within our brokenness. Better yet, we are new creatures with a future and a hope of eternity — unbroken — in Christ.  One day each broken body will be resurrected to a new beauty unimaginable in this life.

Forever restored, we will rise up to dance
a never-ending dance before the very throne of the Most High.  

Praise Him!

This book shares God’s blueprint for children to lead lives full of joy and potential despite autism. It’s the story of God reaching down into the darkness of our lowest moment and pulling us back into the light of His love to soar again.

Autism’s Hidden Blessings (Kregel Publications) will forever change your family walk with autism, allowing you to see your child not through the haze of autism, but through the eyes of an Almighty God Who has provided powerful promises to teach your family to soar above it to an adventurous life of joy and potential.

See this video for more information about why this book is different:

What people are saying about the book:

Kelly Langston offers a lifeline of faith to every parent who has ever wanted to drop down on the floor and throw a tantrum with a distraught autistic child. There is hope. There is help. There is a light at the end of the dark tunnel you are in right now. With compassion and wisdom, Kelly leads the reader through her family’s journey to help Alex. I highly recommend this book to every parent dealing with the confusing maze and emotions of autism.

Glynnis Whitwer, author of work@home, and When Your Child is Hurting.

“What a beautiful encounter. I am filled with tears of joy right now…and I have needed them so badly. I am wracked with fear that my little Nathan will not understand the things of God. Will he ever understand what Jesus did for him???? God is so much bigger than autism. His ways are so above anything. God Bless you!!!!!” (from Deanne)

“Sometimes, we don’understand why things keep crashing and spiraling downwards, but I believe, that’s God’s way of turning our faces unto Him so that we may focus on Him completely, and so that when He has His divine touch on Alec, we KNOW it has to be God”.  (from Jan)

“I found your website from NBC and it is wonderful. My son Tristan, now six, was diagnosed four years ago. I admire your dedication, determination and positive perspective in helping your son and other families”. (from Cyndi)

For more information and additional testimonials, and to find out where to purchase this book, see:

http://www.autismshiddenblessings.com

Ever feel like giving up?  Have you ever wanted to throw in the towel?  Most of us have. I know I have…even today.  Today’s promise gives us a reason to keep going, and promises a harvest … at just the right time … if we don’t.

This year, I will be starting a series of short videos focusing on the promises of God.  I am a strong believer in promised-based living.  Each of these short video posts will feature a single promise.  I will also be posting scriptures with discussion on why we can trust the Promise Maker.

Here’s today’s promise.  Rest on it today!

Promise Links: Galatians 6:9-10 (HCSB)

So we must not get tired of doing good, for we will reap at the proper time if we don’t give up. Therefore, as we have opportunity, we must work  for the good of all, especially for those who belong to the household of faith.

Galatians 6:9-10 (Message)

So let’s not allow ourselves to get fatigued doing good. At the right time we will harvest a good crop if we don’t give up, or quit. Right now, therefore, every time we get the chance, let us work for the benefit of all, starting with the people closest to us in the community of faith..

Galatians 6:9-10 (Amplified):

And let us not lose heart and grow weary and faint in acting nobly and doing right, for in due time and at the appointed season we shall reap, if we do not loosen and relax our courage and faint.

So then, as occasion and opportunity open up to us, let us do good [morally] to all people [not only being useful or profitable to them, but also doing what is for their spiritual good and advantage]. Be mindful to be a blessing, especially to those of the household of faith [those who belong to God's family with you, the believers].

Commentary: Matthew Henry

“We are all very apt to tire in duty, particularly in doing good. This we should carefully watch and guard against. Only to perseverance in well-doing is the reward promised. Here is an exhortation to all to do good in their places. We should take care to do good in our life-time, and make this the business of our lives. Especially when fresh occasions offer, and as far as our power reaches.”

Conditions:

The “proper time” may be in this world…or the next.  The condition of a harvest is that we do not give up.

God as Designer on a Molecular Level:

I remember looking at vivid slides of cells, proteins and molecules in a presentation by Dr. Elizabeth Mumper that were so strangely beautiful. Sitting there, I could scarcely breathe as the as I took in those images. They seemed …so…divine.

Human Neural Stem Cells
Credit: Corey Seehus, BrainCells Inc., USA

These cells are so small that a subcellular imaging system is necessary to capture their beauty. Who can create such a complex, intricate beauty on such a infinitely small scale?  GOD CAN.

God as Designer of the Universe:

The Crab Nebula
Credit: NASA, ESA, J. Hester and A. Loll
(Arizona State University)

The above picture of the Crab Nebula was taken with the Hubble Space Telescope, a project of international cooperation between NASA and the European Space Agency. Located at a distance of about 6,500 light-years from Earth, the nebula has a diameter of 11 light years. (A light year is equal to just under 10 trillion kilometers.) It expands at a rate of about 1,500 kilometers per second.

Do you see what I see?

He’s the Designer of All Things: Big and Small!

It is hard for my mind to grasp just how incredible God is.  God’s handiwork extends throughout the vastness of universe. And yet, He is present in the minuscule details on levels that we cannot even see or begin to fathom.  My expectation is that just as God has designed the immenseness of the universe, He is also the artist of infinitely small details.  Mankind will never be able to fully comprehend just how great God is!

The heavens declare the glory of God,
and the sky proclaims the work of His hands.

Day after day they pour out speech;
night after night they communicate knowledge.

Psalm 19:1-2