IS GOD LISTENING?! Am I? (Guest Blogger Ben Burns – www.gradguides.org)

I don’t know about you, but when my teenage daughter starts getting emotional, I start praying for the Second Coming.

One night she was very anxious about a test the next morning. She is a straight A student and worries a lot about her grades. She was making an A+ in this particular class and had been studying very regularly for the test. However, she was in tears that she might fail the test, which in her mind is anything below an A.

As she was crying, I was thinking, “Are you kidding – you’re a straight A student? It’s just a stupid test and you’ll probably ace it anyway. C’mon. This is, like, so Junior High. Just snap out of it, will ya?”

She could tell I wasn’t listening. She could also sense what I was thinking by the look on my face. That not only made her pull away from me, it now added shame to her feelings of anxiety.

How do you think God listens to us?

Do you think God really listens to our prayers, or do you think He skims them the way we skim blogs, listening for the big ideas? “Okay, what do we have today – ‘new job, ‘need patience, ‘lust control’ – I got it.” When David fumed about how much he hated his enemies, did his honest emotions make God uncomfortable? Do you suppose the Lord was thinking, “David, asking me to crush someone’s skull is not a very nice thing to say, so stop it.”

I think God wants to hear all our honest emotions. I really think He listens not only to what we pray, but to the emotions behind what we pray. Just before Jesus raised Lazarus from the dead, John tells us that He saw the tears of his sisters and responded to their pain. The text tells us simply, “Jesus wept.”

What’s astounding to me about that passage is that Jesus knew He would be resurrecting Lazarus in a matter of minutes, but He still identified with their feelings. He didn’t say, “Ladies, believe in my sovereignty,” or “Stop your crying and trust Me,” or “Now, now, everything’s going to be okay.” He cried because they were sad.

He wasn’t reacting – raising Lazarus was part of His original plan; it’s why He waited until Lazarus was dead before He returned. He wasn’t manipulated – the sisters’ grief was genuine sadness and even anger at His tardiness. Rather, Jesus was attentive to their words and tears. He listened to their emotions and was moved.

I want to become a man like that toward my daughters, my son and my wife.

M. Scott Peck in his best-selling classic, The Road Less Traveled, said that the greatest way we can show love to others is by listening to them. John Gottman amplifies that thought in his book, Raising An Emotionally Intelligent Child. He says that our kids pick up our values the most when they see how we tend to them when they are experiencing their worst emotions: anger, fear, anxiety and sadness.

I would put it another way. Our kids develop their view of God by how we attend to them when they are emotionally vulnerable. Their understanding of the gospel is largely shaped by their experience of the gospel through us. We show our kids what God is like by how we listen to them.

When my daughter gets emotional now I find myself not praying for the Second Coming, but for Jesus’ example of listening to become real in me.

Ben Burns encourages High School Students to stay strong in the faith – check out his website for more details and for how you can invite Ben to YOUR school! www.gradguides.org

DIFFERENT DREAM – PARENTING (BOOK by Jolene Philo)

The exciting news that “you’re going to have a baby” comes with great anticipation and joy in most cases. BUT….when you hear the news, “Your child has special needs,” there is simply no way to describe the devastating thoughts, feelings, and worries that go through your mind and heart all at once.

Perhaps some of the most difficult thoughts going through the minds of parents when first hearing those words are:

  • What are we going to do?
  • We know nothing about raising a child with disabilities. How will we know who to contact for help?
  • What are the steps needed in his/her development to get them to where they can be at their best potential?
  • How do we talk to doctors, teachers, etc. when we don’t know the “lingo”?
  • Will there be someone to walk us through how to make contact with agencies that can be of help to us?
  • How will the siblings handled things?
  • Is there a way to prepare for schooling for my child and the meetings that are needed?
  • How can I handle all the paperwork that is required for hospital stays, doctor visits, and therapy appointments?
  • What if this child dies? How will I handle the emotions, the grief, the planning of a funeral?

For many of us, whose child with special needs is grown, there was little “out there” to address any of the above questions. It took many phone calls, trial and error, asking hundreds of questions, talking to other parents, and many hours of hard work to get the answers we needed.

Jolene Philo in Different Dream Parenting addresses and answers each of the questions above and so many more. Her book is a resource that will cut down your time and effort because of the homework she did for you. She deals with facts and feelings, equipping and education, has researched so you can be organized and productive, introduces you to great resources, and leaves no stone unturned as she brings the reader from chaos to calm. If you desire services, governmental programs/assistance, encouragement, resources, education, church related help….well she’s covered it all.

Hot off the press from Discovery House, this book will answer your questions, encourage you in your parenting, and set you up for success. Few books will guide you like this one will!  More valuable information can be found through: www.DifferentDream.com and you can purchase the book through Amazon, at the Barnes & Nobles website, via christianbook.com, and the publisher’s website www.dhp.org. It “delivers”!

Inclusion Fusion!

UNEXPECTED JOURNEY – When Special Needs Change Our Course

Authors: Joe and Cindi Ferrini

(Articles, books, access to interviews at the end of this article)

 MARRIAGE MATTERS-and so do other relationships!

Imagine five people lying side by side on the waterbed, Lavoie said. If one person moves the whole family feels it. “If there’s a special needs child, that bed can really get moving.” A learning disability can also create discord in a couple’s marriage, he said. The divorce rate in the U.S. is 50 per cent. But in families with a learning disability it’s closer to 70 per cent. (Authors note: and since then some say, 80%)
Sarnia Observer (Ontario), 11/8/05
 

Because of these statistics, many are single parents, but whether single or married, we need the support of others.

Building a strong marriage needs to be done in all aspects of that marriage:  emotionally, physically, and spiritually – and its hard work! This short blog will share some tips that will also coincide with the INCLUSION FUSION Nov. 3-5. A “stay at home” conference with Key Note speaker Chuck Swindoll: http://drgrcevich.wordpress.com/2011/09/07/announcing-our-keynote-speaker-for-inclusion-fusion-2011-chuck-swindoll/

In order to make marriage work, Joe and I have had to Divide and Conquer! That would mean splitting up and one of us accomplishing something while the other “mans the fort”. It’s not always our first choice, not fun, but it’s what works! The idea for YOU, is to consider how this technique would work for you. Here are a few ways we made it work: 

1-      In the early days, one of us would go to church. The other would stay home with Joey (and our girls, sometimes). The one at home would bundle up and pack up the car with the children, meet whoever was at church and trade places. That worked during those years when we could have Joey with us IN church and when there was no place to put him AT church.

2-      If Joe was asked to speak somewhere or meet with someone, I’d be the one to manage things at home, and he would do the same for me when I’d have opportunity to go out.

Additionally it’s important to Pamper Your Marriage!  We can’t do life as usual for very long without some kind of relief from the pressures of caring for another’s full-time needs. You can join at INCLUSION FUSION for the full topic, but here are a few ideas to make marriage work when one is caring for another with special needs:

 Plan intimacy

 Take time to sit and talk, hold hands, take a walk

Grocery shop together and make a recipe together.

Plan a weekend away when you have opportunity. Just don’t forget to come home.

Talking Things  It Out is crucial to a marriage. That takes time. Here are a few ideas (more will be shared at INCLUSION FUSION) that will help you think what might work for YOU:

 Write out “care issues”

Talk through decisions until mutually coming to an agreement (working through smaller pieces of the decision rather than the big chunk)

Offer solutions without judging or jumping to conclusions

Show respect for each other’s ideas

FAMILY RELATIONSHIPS certainly include extended family – the children we have and our own siblings. This relationship can be tricky because we to accept help but not take advantage of those who offer help.

We wanted all of our own children to be treated the same but knowing there are some things the person with special needs would need that they won’t. Because of that, we were careful not to ask or expect our own children to care for our son unless we asked them to do so like we would of a babysitter, and then followed through with also financially compensated them. We never wanted them to feel obligated all the time to care for their brother.

We made sure to have family rules, which included the Golden Rule in Matthew 7:12, “Therefore, whatever you want others to do for you, do so for them” and Mark 12:31, “You shall love your neighbor as yourself. There is no other commandment greater than these.” If we could follow that, we thought we’d be able to set a good example for our children, neighbors, teachers, etc. Also, we always desired to work as a TEAM (Together Each Accomplishes More).

Family meetings and goal planning were always tops on our list as a family, so we knew we were all on the same page, and no one could say they felt left out or unimportant. Everyone had a “say” at our meetings!

OTHERS:Friends , teachers, aides, administrators, people at church (see: http://www.keyministry.org/  and http://www.joniandfriends.org/church-relations) are folks to keep near us for the well being and help in development and learning of our child with special needs. Our goal? BUILD BRIDGES rather than BURN BRIDGES. These people will give us help in getting to the next step of life. Not everyone will be able to help and be a part of our child’s journey, but it’s important to give as much help and advice (to those willing to learn) so they can be of help and assistance for YOUR life journey. Not all advice we will receive will be helpful, but we can accept it, try it, and use what works – disregarding the rest.

We look forward to being with you Nov. 3-5 at: http://drgrcevich.wordpress.com/inclusion-fusion-2011-speakers-and-topicsjoin us, will you!?

Articles by and Interviews with Joe and Cindi:

Familylife Today – 3 days of programming called Unexpected Journey from their book (2/09) UNEXPECTED JOURNEY – WHEN SPECIAL NEEDS CHANGE OUR COURSE

June 29, 2009 Dennis Rainey and Bob Lepine interview Joe and Cindi on FAMILYLIFE today radio. Topic: Facing a Painful Reality:
http://www.familylife.com/site/apps/nlnet/content3.aspx?c=dnJHKLNnFoG&b=3789887&ct=7133605

June 30, 2009 Dennis Rainey and Bob Lepine of FAMILYLIFE TODAY interview Joe and Cindi. The topic is: Embracing Life’s Changes: http://www.familylife.com/site/apps/nlnet/content3.aspx?c=dnJHKLNnFoG&b=3781143&ct=7048085

July 1, 2009 Dennis Rainey and Bob Lepine of FAMILYLIFE TODAY interview Joe and Cindi on the topic, “Love: A Day to Day Assignment”:
http://www.familylife.com/site/apps/nlnet/content3.aspx?c=dnJHKLNnFoG&b=3781143&ct=7133605

Online Broadcasts:

Start Your Family: Becoming Parents of a Special Needs Child: (An interview with the Ferrini’s)

http://www.startyourfamily.com/2009/05/becoming-parents-of-a-special-needs-child.html

Need Project: – UNEXPECTED JOURNEY: (Ministry NEED PROJECT)

http://www.needproject.org/casts/podcast1033.mp3

Focus on the Family

FOCUS ON THE FAMILY –Special Needs and Marriage – module of 1 overview and 6 articles in a series for their on-line magazine: http://www.focusonthefamily.com/marriage/marriage_challenges/special-needs-and-marriage.aspx

Excerpt Article from UNEXPECTED JOURNEY – WHEN SPECIAL NEEDS CHANGE OUR COURSE – one article in a series: http://www.focusonthefamily.com/parenting/parenting_challenges/parenting_a_special_needs_child.aspx

 

RADIO: Focus on the Family interview taped July 20, 2011 for airing January 2012.

BOOKS:

Unexpected Journey, When Special Needs Change Our Course – Dr. Joe and Cindi share their journey of caring for their son with special needs and their parents with Alzheimer’s.

Balancing the Active Life – an interactive Bible study for anyone of any age – the goal of this 13-week study is to challenge and encourage the participant to prioritize the activities they believe are the most important in their life, with Christ being the center and the focus of all that they do.

Get it Together – an organizational planner

‘Tis the Season – a Christmas planner to keep the holiday less stressful and more meaningful

Online Broadcasts: 

Start Your Family: Becoming Parents of a Special Needs Child: (An interview with the Ferrini’s)

http://www.startyourfamily.com/2009/05/becoming-parents-of-a-special-needs-child.html

Need Project: – UNEXPECTED JOURNEY: (Ministry NEED PROJECT)

http://www.needproject.org/casts/podcast1033.mp3

WEBSITE: www.joeferrini.com

                         www.cindiferrini.com

Email us via our website!

DON’T HAVE KIDS…..

DON’T HAVE KIDS IF YOU WANT:

A sleek hairstyle before noon – or realistically, until Sunday, and then don’t count on it!

Sleep – for a few years – OK, maybe even up to 20 years…hmmm….maybe more. It will depend on many factors.

Manicured fingernails and/or pedicured feet and nails even for special occasions.

Time of your own to do as you please – ever.

Clean clothes without permanent stains.

Money for you to pamper yourself.

A full conversation with your spouse, a friend or even with the deli-worker.

A clean and tidy home that is always in order.

Clean windows.

Calm and order.

To finish your thoughts.

CONSIDER HAVING KIDS IF YOU:

Like the “wind-blown” or “Au Naturale” look in hairstyles and clothing!

Can sleep with one eye closed and one open and call it a good nights’ sleep!

Like a mani or pedi that lasts for 2.5 weeks – AKA chipped nail polish.

You are willing to give of your time, talents and treasures, because kids will take it ALL….all through college. Remember: The sucking reflex is common to all mammals at birth.

Like vintage clothing (AKA garage sale specials, hand-me-downs, and thrift shop deals…) for YOU, not just them.

Can consider the fingerprints on the windows as part of the art collection you wish you could afford for your focal point wall.

Can get into the groove of chaos and commotion – AKA “hold on for the ride!”

Know you and your spouse will need to “talk later” and can postpone that conversation indefinitely!

Don’t care about finishing a sentence, a thought, a sandwich, a meal, a book, folding a full basket of laundry, emptying the dishwasher in one attempt, having a full phone conversation, getting a once a week date night, etc.! (Once you hit menopause, it will all blend together and you will simply forget what you started or simply not care. Trust me.)

You want GRANDCHILDREN…because then, you just start it ALL OVER, and you will be amazed at how much fun it is….AGAIN!

BOW TO THE VOW!

Whatever happened to keeping ones marriage vows?

I watched the less than 3 minute answer Pat Robertson gave when asked: “My friend’s wife has Alzheimer’s and does not recognize him, he is seeing another woman because of this, what should I tell him?” You can check out the link to hear his full answer. It won’t take long: http://www.cbn.com/media/player/index.aspx?s=/mp4/BIO_091311_WS

Robertson gives us plenty to think about in his short answer, but I believe if we take our marriage vow(s) seriously, we will bow to the vow. Sacrifice, yield, commit, bow to the vow(s) we shared. Pat Robertson talked about how hard it was to care for “someone like this.” It’s more than hard. It’s self sacrificing. It’s exhausting. It has little reward because the person you care for doesn’t have the potential or capacity to give anything in return. Anything. I watched Mom care for Dad for over 6 years along with my 2 sisters and I. We lovingly sacrificed our “own plans” and spent countless hours changing dad’s diapers, giving him haircuts, staying at his side during numerous nursing home or hospital stays, feeding him, trying to make sense of non-sensible thoughts and words, yet always choosing to bring him home to where he seemed to be most calm (i.e. less agitated and frustrated. Less being the operative word). The home that accommodated my dad, the family care-givers and a night time care-giver – so Mom could sleep – was remodeled to accommodate his hospital bed, walker and eventually the wheelchair, and other needs.)

Accommodate: To make fit or suitable; to adjust; to provide with something needed; obliging. To help understand “accommodation” as it relates to Alzheimer’s is rearranging your whole life to help someone besides yourself to be comfortable and well cared for.

While I don’t agree with much of what Mr. Robertson said, I do agree that it’s hard. The person “isn’t there” most of the time, but sometimes they are, and when they are, you grasp that moment and savor it. We didn’t stop caring, helping, or visiting just because there was little to no response from Dad – or because it was inconvenient, hard, or wasn’t fun. It was never convenient – it was always hard and it was seldom fun. Picture changing an adult diaper; picture an elderly person throwing a temper tantrum and food or objects. Picture yourself helping. Can you do it for the long haul? Even if the long haul includes daily visits to a care facility that can help you?

I suspect Mom’s 6+ years of care-giving may have precipitated her early death (heart attack at age 69)….Dad giving up and following his bride in death just 5 days later. But each of us did what we did because of one thing: LOVE – which when sincere and genuine carries with it a commitment. It was hard. Very hard. But love was stronger than the challenge. It always is. Robertson’s response takes me by surprise given his years of ministry. I understand the bible to teach that (true) love never fails…is patient, kind, does not seek its own, bears all things and hopes all things…to share a bit of I Cor. 13: 4-8.

As difficult as those years were, we were somewhat prepared having cared for our son with special needs (who is now 30). Would we walk out on him? Not a chance. God never said it would be easy, fun, or comfortable. Less than a year after my parents’ deaths, Joe heard the doctor say, “Your Mom has advanced vascular dementia.” We had a new, but not so different choice to make: stay in the game, sit on the side lines, or leave. It took but a moment to catch our breath and get back in the game. AND….wouldn’t we all hope that our spouse would desire to stay in the game and care for us…for BETTER OR WORSE – and bow to the vow? I know I do.

©Cindi Ferrini, www.cindiferrini.com

LeBron and the “R” Word….

BOSTON (AP) – “LeBron James says he’s sorry for using the word ‘retarded’ in a postgame news conference.”

I was eager to see if there would be a follow up broadcast to that comment. Indeed, LeBron later apologized for using the “R” word saying, “If I offended anyone, I sincerely apologize.” I’m pretty sure I can stand in the front of the line with many whose children have special needs and say, “It’s not IF you offended anyone.” You did.

When that word is spoken, those of us in that “circle” try to be gracious to spare others embarrassment -  but we hear it. And we heard you.

The apology would have been better phrased, “To those who care for the special needs population of the mentally disabled/challenged (mentally retarded), I am very sorry for my insensitive comment. I understand my comment may not be understood by those who are challenged mentally, but I do understand that I have deeply offended those who care 24/7 for those with special needs of this kind.’

Furthermore, I would love for LeBron (and others who use the “R” word) to offer public service to those who are mentally challenged, to learn what the special needs world of “effort” looks like. Those who have trouble learning, speaking, holding or throwing a basketball or baseball have likely spent hundreds if not thousands of hours in PT (that is Physical Therapy), OT (Occupational Therapy), and SP (Speech Therapy) only to get to a less than hoped for outcome after many years of hard work. These therapies are not working out to better prepare an athlete after a sports injury, rather these therapies are helping the patient to learn to do some of the very things we take for granted. OT helps those who are mentally slow to learn to use their fine motor (fingers and hands) skills for something as noble and simple as feeding themselves. PT was very helpful in teaching my son to balance because he couldn’t sit up on his own – that took a good year and a half to accomplish that one skill. ST was something that took some 12 years in the making to get my son to a point where he could make and form words. Just 12 years.

Yes, all those things took place at the rapid speed of what Webster calls retarded: “slow or limited progress.” Many who are “mentally challenged” or “retarded” have worked like an athlete to achieve little to no recognition; instead they’ve earned the cheers and applause of their parents, siblings, teachers, therapists, (and some family and friends), as they accomplish the mundane.

I could write on and on, but everything else has already been written in the book my husband and I authored: UNEXPECTED JOURNEY-When Special Needs Change our Course. If LeBron is man enough to ask for it and brave enough to read it, I’d send a copy to him free.

“SHARE” this message and let’s see if he’ll ask. Until then, I commend and applaud those caring for those with special needs. May you “go the distance” with grace and dignity - because I know it’s not with ease or comfort!

And JFYI – I’ve waited 30 years to write this – and it’s written with hope to initiate change in how the the “R” word is used.

One who knows,

Cindi Ferrini

www.cindiferrini.com

Get A LIFE!

Get a LIFE!

I’m often tempted to say that! I want to say that when:

  • When things aren’t going my way I think, “Wow, if I could just get a life!”
  • When frustrated, I sometimes say, “This is life?”
  • As a young mom changing diapers I’d catch myself thinking, “This is not what I thought children were going to be all about. I wonder when I’ll get a life.”
  • When our son wasn’t developing on schedule and we’d be doing the same therapy for the trillionth time, I’d sometimes say, “I just wish someday he’d get this, and get a life.”
  • When others don’t get in line with our wishes we sometime say, “I wish they would get a life!”

I guess it’s true that the grass is greener in someone else’s yard, but do you ever feel stuck in yours?

It would be such fun to be able to pick up and take off – to the other side of town for dinner – without calling on someone to care for our 29-year-old with special needs. It’s not an easy task to find someone to “fill that bill.” A teenage (boy or girl) would not be appropriate to watch our grown son. A “service” to bring a stranger to care for our son (who would not be able to tell us if anything went wrong), is not a comfortable option.

I’d love to be able to travel with my husband like we had dreamed when we were younger. But if a night out is hard to accomplish, a week is not much easier. And it would be such a treat to say “yes” to friends who are going to see a movie or go to a play – last minute!

Oh…If I could just “Get a LIFE!”

But, while the grass is often greener on the other side, I face the fact that life is different for us than for some of those around us and that we have choices to make. And for us (and you) choosing what we feel is right means choosing what we value. It’s that simple and it’s that complicated.

In our society we want to fix things so life is not interrupted or inconvenienced. If we could take a pill to make everything perfect, we would. Because no pill can cure us from challenges and struggles, we have to decide what we value because that’s how we’ll decide what we’ll do. For us the reality and choice was valuing and caring for our son, and the knowledge that doing so would last a lifetime – either his or ours.

So how does that look today? As a woman who now has grown children and one grandchild, I thought I’d have outgrown this saying, but sometimes I find myself seeing others in retirement doing what we’d hoped, and hear myself saying, “I wish I could get a life!” But on good days – and most of them are, I realize that all of us have times when things don’t go our way, and we all have to “grow up” and learn to go with the flow. I occasionally get frustrated, or feel sorry for myself, but see many of my friends do too – their frustrations are just a different flavor. And, we all look back on those mundane days of childrearing – doing the same thing over and over again with much fondness, and sometimes with a secret wish to return to or re-do a few of them!

I realize I do have a life. It’s one that includes caring for our son who has brought so much to our marriage, family and life. It’s about being tethered to home more than we thought we would, but being able to look out over our beautiful wooded back yard and say, “I’m pretending to be on vacation today,” while reading a book and sipping my Café Vienna, or actually traveling somewhere but keeping in mind the pace will be very slow with Joey at our side. It’s about being thankful for a sweet handful of family and friends who stand in the gap to care for our son when we have opportunities to speak at conferences or for ministry. It’s about recognizing we’ve met wonderful people that we wouldn’t have, had Joey not been given to us. It’s a romantic dinner for three, which still means I don’t have to cook!

Yes, I’ve come to realize that while we all want to “get a life,” we wind up finding that the phrase just needs to be reworked: “This IS our life!”And it’s really pretty special.

Fidgeting in Prayer?

Philip Yancy writes in his book Prayer: Does it make a Difference? “Why does prayer rank so high on surveys of theoretical importance and so low on surveys of actual satisfaction? What accounts for the disparity between Luther on his knees for several hours and modern prayer fidgeting in a chair after 10 minutes?” He goes on to explain, “In former days farmers prayed for ends to the drought. Today we await the weather forecast. In the former days ill children were prayed for by their parents as they cried out to God. Today we call the ambulance or phone the doctor.” He asks, “How can we ask the Lord to give us this day our daily bread when we have a pantry full of a months’ supply of provisions?” He comes to the conclusion that we need to see prayer as a privilege and not simply as a duty.

Perhaps you have learned as I have, that prayer is conversation with our heavenly Father, and we have the privilege to communicate with Him whether on our knees – reading the bible and praying, or while driving around town and running errands. There are times where focus and attention must be direct and purposeful and I am called to be quiet and listening and other times, I can be “thinking” and praying at the same time, but not with the same kind of attention as in my quieter moments. I know God wants to hear from me at all times, and He is always ready to listen. He also tells us that we should:

  • “pray without ceasing” (I Thess. 5:17)
  •  Sometimes we pray in secret (Matt. 6:6)
  •  Other times He asks us to pray publically
  •  Pray for one another (James 5:16)
  • Pray for those who suffer (James 5:13)
  • Devote ourselves to prayer (Rom.12:12)

 

How we are doing at what He’s telling us to do? Do you know someone who needs prayer? Let’s get busy and stop fidgeting!

WALK A MILE IN THEIR SHOES

 As many of us embrace February for the “love” factor, I’d like to spur our thoughts in the direction of what we do to make “love” happen – especially in the framework of those whose lives are often dismissed, ignored, disregarded, neglected, slighted, snubbed – those with special needs.

 Perhaps you, like I, have missed the opportunity to show compassion or love to someone simply because they have special needs and we don’t know and don’t seek a way to connect with them. Perhaps we have no idea how to engage in conversation with them or their caregivers – no idea how to, well, walk a mile in their shoes!

 When our son was a few years old, my husband was finally able to express his fear and disappointments regarding the handicaps and challenges that were a part of our every day existence and of concern to us and our sons’ care. It wasn’t easy for him to share his heart, but did so through tears, only to hear the cutting words of the listener, “I thought you were tougher than that.” That was the last time he shared anything about our son with that person, and for that matter, with few others for many years.

 If we truly walked a mile in other peoples’ shoes, we’d quickly understand what they have to deal with. We’d become aware of the hot button issues that tick them off, and we’d become sensitive to what makes them tick. We wouldn’t have all the answers.

 We wished we could have had people to talk to when our son was small.  The people we reached out to were probably not equipped to mentor or help us. For that reason, we desire to mentor couples with young children, to listen to their challenges, to cry with them, and to encourage them.  Sometimes listening to their struggles is difficult because we relive in our minds the complexities of our early years; however, the positive outcome is that with the help of the Lord in our lives, we make it; and in turn we can give them help and encouragement to make it too.

 Every time we feel as if we want to quit, we remember that we are called to this purpose and that God did not make a mistake. Maybe we can help others who have a similar life situation as we do but who are a few steps behind us in their journey, or perhaps we can simply be one who’ll provide a listening ear if we are not in the same life situation. We just need to be willing. Willing to extend the love and compassion that person needs for the moment.

 Ask yourself:

  •  Am I willing to be a listener to someone who has a challenge different than my own?
  • What would it take for me to approach someone with special needs (and/or their caregiver) and ask how I might help or pray for them this day?
  • Might I offer to assist in a “caring” capacity at church by watching a child with special needs (thus allowing the parents a time of uninterrupted time to sit in church together?)
  • Take a moment to observe what you see. What must their lives be like? Sit quietly and contemplate how you would “do” your life, given what you are observing. Then take a moment to contemplate the things you aren’t seeing (meal times, bath routines, temper tantrums, sleepless night, medical issues, etc.)

 

Remember that their work is not 9-5 but 24/7. We might just provide them with the love and compassion they need to keep them going…all because we took some time to WALK A MILE IN THEIR SHOES.

The EYES have it!

My husband had finished his requirements for graduation from dental school at THE Ohio State University, and was given a menu of options and opportunities regarding where he could spend some discretionary free time. He chose to work at University Hospital in Columbus, Ohio, doing dentistry for children with special needs. He was taught in dental school to look into the eyes of his patients to be sure they were not experiencing any discomfort (okay, pain) as a result of whatever procedure was being done. What he noticed when looking into the eyes of these children with special needs, was how absolutely beautiful, even captivating their eyes were. It wasn’t just the color of their eyes, or the fact that some of them couldn’t even focus their attention on something. It was just “that look”. For most of them, the only communicating they could do was with their eyes. It was fascinating to him to watch their eyes as he worked on their teeth.In the early years of our marriage and his dental practice, he worked in a few nursing homes whose residents were children with special needs. Dealing with drooling patients with flailing arms, squealing with uncontrolled emotion, was very sobering. It was challenging from a dental perspective as well as an emotional perspective. He was always thankful to come home where things were calm and “normal.”When our son Joey was born he seemed quite “normal”, but one night, Joe was caring for Joey so I could get some needed sleep. Joe scooped Joey out of the crib like he’d made a great football catch and took him into the family room to play on the floor for a bit. As he rolled Joey gently back and forth, even rolling a ball to him, attempting “catch” with his infant son, he caught a glimpse of Joey’s eyes that took him back to his experience at University Hospital. He knew “that look”. He picked Joey up and held him close, saying, “Oh God, not my son!” What Joe knew that night, I was not yet seeing. I noticed that Joey wasn’t doing the things others his age were doing, but the doctors assured us he’d catch up. But the truth was this: instead of catching up, the gap kept getting bigger in what he could do and what he should have been able to do. For Joey’s first birthday, a few of my gal friends and their children gathered at the home of my parents for a little picnic. All the other children were running around their property, throwing stones into the pond, and eating a kid friendly lunch by themselves. What a shock it was to me that Joey could do none of that. He sat is the high chair, had to be carried everywhere, and needed help putting food into his hand. A dear friend, whose son was a little younger than Joey, but running circles around him, privately chatted with my mom about the boys. She shared her concerns about Joey. Because she cared enough to share in such a loving manner, it prompted us to begin asking some difficult questions of the doctor and pursue testing. It must have been difficult for her to bring up her concerns, but what a loving gesture that was. She was often the one to call me at just the right times – when I’d gone through a rough day – listening to my concerns, allowing me to cry, and encouraging me.Sometimes we want to deny what we see. We want to close our eyes, and pretend what’s happening isn’t. We want to turn our heads the other way or even go to sleep. But denial won’t get the help that’s needed. We need to open our eyes, and move forward. Once we accept what we are seeing, we can begin to take the necessary steps to seek the right doctors and diagnosis – getting the help that will allow our child to learn all they can. The earlier the recognition and acceptance, the earlier we can get help, and the better chances the child will have to gain the kinds of skills and learning they’ll need to make it in this world.

I’ve been on this journey for 29 years and counting, so I’ve had many opportunities to look into the eyes of parents and children. What is very difficult and challenging in the early years, can indeed become a great blessing later on. Today, if I’d be asked to vote whether I’d take this journey again, I know I’d raise my hand and say, “The eyes have it!”