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Showing posts with label auditory processing. Show all posts
Showing posts with label auditory processing. Show all posts

Thursday, August 25, 2011

I Need Eleven!

Have you ever been baffled or surprised by something your child says? You may be certain that you heard the words correctly, but they don't make sense. Having children with learning struggles, I often found that I needed to clarify both what I said to my children and what they were communicating to me. With a combination of ADHD (attention deficit hyperactivity disorder) and auditory processing difficulties, communication was often a challenge. First, I had to obtain and keep my child's attention long enough to convey a message. Then I had to determine if the message had been accurately received. If distractibility and impulsivity didn't interfere, we could have a good conversation.

Children with learning disabilities often have unusual ways of expressing themselves. My son Josh had some word finding difficulties, so he would refer to the ankle as "that wrist part of your leg". Likewise, the elbow might be "the knee of your arm." Once when Josh wasn't feeling well I asked him to describe his symptoms. He often used vague and nebulous words to tell me what he felt. I felt like a detective who needed to ask just the right questions to get my suspect to tell me what I needed to know.

One time, though, Josh told me his throat was sore and described what he was feeling in this way, "I feel as if my uvula has been acided off". (I like the "uvula" part - true son of a speech therapist!) This description, although no doubt atypical for most children, painted a clear picture of the location and degree of Josh's discomfort and indeed it turned out that Josh had strep throat. "Acided" may not be a real word, but it sure got the point across. Josh usually sailed through illnesses with little response to pain, so when he complained I knew it was serious.

When children are infants, we fret because they are not able to tell us what is wrong or where they hurt. We think how nice it will be when they are able to talk and tell us more exactly what they feel. If a child is a late talker, nonverbal, or has difficulty with expressive language we have to continue interpreting possible meanings to whatever communication attempts our child is able to produce.

My daughter Beckie was a big talker, and it was easy to tell that when she wanted "lunch fries" she meant "french fries" and that her "Valentime" was a "Valentine". Since she had auditory processing issues, she said things the way she heard them and I continued in my role as communication detective to determine what Beckie was trying to convey. This was somewhat complicated by the fact that Beckie chattered a lot and was not always looking for a response but rather was processing her experiences by speaking out loud.

When she was a preschooler I noticed a frequently occurring phrase, "I need eleven!" Eleven what? I tried to figure out if she was trying to practice her counting skills, trying to collect something, or was just repeating something she had heard. But where had she heard it? Beckie was always a cuddle bunny, and was frequently snuggled up in my lap while we read books or talked. I tried to become aware of the context when she "needed eleven", but couldn't narrow it down. She said it contentedly when she was climbing onto my lap or getting a hug. She said it when she was physically hurt and when her feelings were hurt. When I asked her if she wanted to count to eleven together, she happily replied in the negative and wrapped her arms around me for a tight squeeze.

One day Beckie had been visiting one of her best friends for a play date, and I went to pick her up. She and her friend were sad to have to part ways, and the other child's mother offered comfort by asking her son if he needed a lovin. I realized that "Do you need a lovin?" was a common phrase in that household, and in Beckie's young mind had been translated into "Do you need eleven?" It had nothing to do with numbers, but had a strong connotation to comfort and the expression of affection. Since I had responded in ways she needed despite my lack of understanding about what she was saying, Beckie was inadvertently effective in her communication with me.

This is just one more reminder that love can make up for so many things. We all make mistakes with our children. We realize after the fact that we erred in our approach to teaching some students. We feel the pressures to convey the right amount of information at the right times while helping our struggling students develop skills to help them be successful. Our curriculum isn't always a match for what we need. Our children may not be progressing at the rate we desire. We lose it. We yell, we apologize, and then catch ourselves being impatient again. We feel inadequate to meet all the needs we face on a daily basis. The stakes are so high.

You've heard it before but it bears repeating. What our children will remember the most is the relationship we have with them, not the specific things we deliberately taught or the strategies we used to help them learn. I blew it with my kids sometimes, and I knew it. I truly believe that my relationship with them is more important than any school subject and thus needed remediation before we could proceed with our official homeschooling. I find it very humbling, yet restorative, to apologize to my children when I have wronged them. They have always been very forgiving and amazingly resilient, a picture of God's grace to me.

Showing grace and respect runs both ways in a relationship. It builds character and will outlast the school years as a child grows into an adult. Have you been focusing so much on getting the school work done that you've lost sight of the importance of relationship? Don't let standards and benchmarks keep you from seeing the individual child who is right in front of you. Teaching a child is a great aspiration, and teaching in the context of a relationship is powerful. Children may not remember everything you've taught them, but they will remember you. Do you have the kind of relationship you want to become part of their lifelong memories? Let's give our children lots of "elevens" and protect our relationships as they grow.

Monday, June 20, 2011

A Mom Like You

In the last six weeks, I've had the opportunity to speak at three different state homeschool conventions. At each conference I attend, I share information about learning disabilities, Attention Deficit Hyperactivity Disorder, Sensory Processing Disorders, and Auditory Processing Disorders. More important than the facts I pass along are the real-life stories from my own family experiences. I share what didn't work as well as what worked at least some of the time. I share some of the failures and frustrations as well as our hard-won achievements.

When my first two children graduated from our homeschool in 2006, we declared our school colors to be black and blue. We were the homeschool of hard knocks! Not only did my children struggle with learning, but I struggled to try to find better ways to teach them. One of the biggest benefits for those attending workshops for children with various special needs is to look around and realize they are not alone. There are others striving to teach children with challenges, and others who understand the difficulties families face when their child has to work harder than most for every small gain they accomplish.

What has always amazed me is how God has prompted me to share some of the hardest, most unimpressive movements of my life and that is what people are blessed by in my workshops. Sure, I offer lots of tips and practical strategies, but what people connect with is hearing a speaker who admits to not having it all together but never gave up trying. My son is a young adult now, and he comes to conferences with me. People look at the two of us as survivors, who dealt with a lot of learning challenges and came out intact. Now Josh can share his perspective, and give parents insight into why their children may act the way they do.

I've never had all the answers to the challenges my children faced. What I did have was a commitment to help them grow into the unique individuals God intended them to become, equipping them as best I could. Sometimes I was out of ideas for how to teach a given topic, and my kids still weren't "getting it". All I had to offer was reassurance that I would keep trying to find ways to help, and would not give up on them. I would be the knot at the end of the rope that they could hang onto. The message was: Mom doesn't have all the answers but Mom will always be there with you, coming alongside until we figure something out.

Don't underestimate the power of just being there for your children. You don't need to know all the answers, but your kids need to know you haven't given up on them. It's in the safety of knowing your love is unwavering that your children find the courage to try again, fail or succeed, and try some more. Our children are far more than what they can or cannot do, and they each have something to offer. This overall supportive attitude has a far greater impact than the best teaching strategies in the world.

Years ago I had a man in his 30's come up to talk to me after I presented my workshop, "Helping the Distractible Child". I don't remember which conference it was, but I will forever remember what he said to me. He explained that as a child he always had difficulty paying attention, and was constantly getting in trouble as a result. He thought he was smart enough, but couldn't sit still and had trouble completing assignments. He tried hard to comply with the demands put on him, but always felt like he was a disappointment to his parents no matter how hard he worked. "I wish I'd had a mom like you," he said. "One who could see the strengths and work with me."

One day all of our children will be adults. I challenge you to be that Mom, the one who never gives up on her kids no matter what. Be that Dad, who is consistently there for his children regardless of their struggles. Be that husband or wife who sticks around during the hard times. Be that person, so that one day your adult children will be able to say, "I'm so glad I had a Mom (and Dad) like you."

Thursday, June 16, 2011

My Beckie, Homeschool Valedictorian 2011

1993 was a monumental year. It was the year I started homeschooling and the year that my youngest child, Beckie, was born. Beckie was the kind of baby who quieted as soon as she was picked up. She always seemed content just to be with people. As an infant, Beckie was perfectly happy with attention from any adult or child. By the time she was a toddler and on the move, she enthusiastically joined in play with other children.

Her brother and sister (Josh and Beth) were crazy about her and wanted to include her in all their activities. They loved to teach her about whatever they were learning and when we were out and about Josh would hold one of Beckie’s hands and Beth would hold the other. Beckie was a very versatile playmate. She loved tea parties, dress-up times, Legos, and playing in dirt. Josh says Beckie is the best little brother he could ever have wished for.

I can still picture Beckie’s beaming smile as she grew up, and remember thinking how very loved and confident she always looked. More than once I thought I could have aptly named her “Joy” instead of Rebecca, because she typically seemed so joyful and brought it to others. It was hard not to smile when Beckie was in the room.

Like her brother, Beckie has dealt with attention challenges (ADHD), sensory processing difficulties, and an auditory processing disorder. Despite these struggles, Beckie has faced them with grace and determination and has experienced success. Today she is a second degree black belt in karate and at the time of her high school graduation she has already completed her first year of college.

Beckie has grown into a lovely young woman. She is compassionate, optimistic, funny, and strong. Her sense of humor and quick-witted observations are delightful. Beckie’s enjoyment when she is with animals and children is contagious. She is a loyal friend and a defender of the underdog. I think Beckie is amazing, and it has been a privilege and a blessing to be her teacher and Mom.

Beckie graduated from our homeschool, the Family Home Academy, on May 22nd, 2011. Congratulations, Beckie!

Monday, June 14, 2010

The Answer is Yes!





Yesterday was a big day for my daughter. She graduated with honors with a B.S. in Education from The Ohio State University. She hand embroidered Jeremiah 29:11 on the top of her cap, and I am very proud of her accomplishments and her perspective about her future. Since I homeschooled Beth all the way through high school, I have been asked by many people through the years if homeschooled students can go to college. Fortunately, with the growth in homeschooling we are not considered to be such a fringe element of society anymore. Many homeschool students have found success in a variety of venues. Beth's graduation from college answers that question with a definitive "yes". College is not for everyone, homeschooled or otherwise schooled. But for those who wish to seek that additional education, homeschoolers can hold their own in any setting. What a joy to celebrate Beth's success!


Of course, it seems nothing goes without a hitch when there's a big event and multiple people involved. Beth's graduation was held outside in the stadium at OSU, and the heat and humidity were both high. Both of Beth's grandparents came to see Beth graduate, but grandma doesn't do so well in the heat. Just after I got a text from Beth saying that she wasn't feeling well and felt dehydrated, grandma passed out in the bleachers. We were able to eventually find the first aid station and she is fine, but we were shook up and spent time in the first aid station while waiting for Beth's turn to get her diploma. With a graduating class of over 8,600 students, it took a long time. We did leave grandma with the medics, at her insistence, and popped back into the stadium to see Beth officially graduate. Because there were so many students, instead of calling their names they tolled a bell that sounded like a funeral dirge the entire time students were receiving the diplomas. My two sensory/auditory processing children were beginning to twitch from the relentless ringing.
Next we drove to a restaurant of Beth's choice, The Cheesecake Factory, but they didn't take reservations and there was a 2 1/2 hour wait. We hunted around for other restaurants in the area, but all had long waits so we headed back home. I had potato salad, a fruit and yogurt parfait, and graduation cap cookies on hand, but that hardly made a meal for eight. So we got carryout to go along with it.

My son, Josh, is an author and he broke out of his usual sci-fi writing mode to pen this "Ode to Beth's Graduation":
Ahem.

Rush so we will be on time.
Walk a mile and then we climb.

Hungry since we walked so far.
Left the food back in the car?

Seated up so very high.
Great view of that cloudy sky.

Now the band begins to play.
Half an hour til the parade.

8,600 tassels tall.
Did you have to name them all?

Graduates who have done your best!
Survive this day and pass the test!

Moving speeches, people sing.
Can anybody hear a thing?

Think it's time to go inside
Before this turns to suicide.

People get their PHD's.
Hangin' out with EMT's.

Additional speeches get carried away.
What? You mean we're just halfway?

More interesting show to watch:
Grandma versus the Red Cross!

Sunburn in the first degree.
People leaving. Wait for me!

Diploma time's a living hell.
Someone kill that funeral bell!

Over? Really? Now we're free!
To the Cheesecake Factory!

Two and a half hour's wait?
Fifty bucks for a piece of cake?

Everything else is crazy as well.
Ten miles around the Hilton Hotel.

Home at last. What a day.
Now we get to eat parfait.

All is over, and I'm glad.
...just what year is Beckie's grad?

Collapse.






Thursday, January 07, 2010

Turn Your Recorder On

My son, Josh, and my youngest daughter, Beckie, both have auditory processing difficulties. Although when they were officially evaluated by an audiologist they had some differences in the auditory tasks in which they struggled, they both demonstrated poor working memory. This means that although their hearing acuity is fine, they process the incoming auditory input in an atypical manner and they are unable to hold information in their minds long enough to remember it all and act on it. So they might remember the first thing they heard, or the last thing they heard, but if it's a long segment they are likely to lose information. I used strategies like pairing visual information with auditory information, and I utilized gestures and demonstrations nearly all the time. I had them look at me before I gave them directions. I had them repeat back to me what they heard so I would know if they were not complying with me or if they never got the information in the first place. This is an important strategy for parents and teachers, because you should not be disciplining a child for not doing what you've asked if he never received the information completely in the first place. I also did activities specifically to work on improving auditory memory and attention. One activity I did with all my children was have them repeat back exactly what I said to them, increasing the length of the segment a little at a time. For example, I would say something like, "The cat walked to his bowl." We would practice that until they could say say it verbatim. The next sentence would be, "The white cat walked to his empty bowl." The next sentence might be, "The white cat slowly walked to his empty bowl, hoping to find it full of food." This stretched their attention span and challenged their auditory memory skills a little at a time. I also reminded the children to make a mental picture about what they were hearing, since the internal visual cues would help them remember details. One day, while doing this activity, I noticed that Josh was tapping himself on the temple every time I started with, "Ready? Listen to this." I thought to myself, "Great! Now on top of the AD/HD, sensory processing difficulties and auditory processing problems, I've given this kid tics!" I wasn't sure I really wanted to know the answer, but I finally asked Josh if he realized he was tapping himself on the head every time it was his turn to repeat something. He promptly said, "Yes! I'm turning my recorder on!" My little hands-on guy could relate to pushing a button to record something, so he had implemented a tactile strategy for himself. (Whew! Big sigh of relief for me since his head tapping wasn't caused by tics after all and I hadn't done anything to cause them or mess up my kid!) Once a child comes up with their own strategy, we can use it knowing that it makes sense to them. After Josh showed me that he identified with "turning the recorder on" I generalized that strategy for other listening tasks. When teaching any subject, I would prompt Josh to turn his recorder on because the next point was very important. Before giving him a multi-step direction, I would prompt him to turn his recorder on and picture himself doing the task. His strategy became my strategy with him, because Josh taught me something that worked for him.

Wednesday, December 30, 2009

Hello Again!


Hello friends! I haven't blogged for awhile, but I'm back now. I've been feeling like the deflated lawn decorations in this yard so I thought I'd take a picture to give you a nice visual symbol as you read. I came down with a cold on November 25th, and it quickly turned into a sinus infection, ear infection, and lung infection for which I've taken numerous medications and...I'm gradually improving but still not over it. My right ear drum perforated and I've been like the auditory processing struggler who says "Huh?" for the past several weeks. I've decided to try to get back to some of my regular activities and hope that full recovery will happen ANY DAY NOW. There's never a good time to be wiped out of commission, but I think the month preceding Christmas was especially inopportune. This is the first year that I've ever been unable to get Christmas cards sent before Christmas. I started my gift wrapping the day before Christmas and recruited my family (okay, "coerced" would be a better word) to help with the wrapping and food preparation. Did you know you can wrap gifts for someone with AD/HD while they are in the same room as long as you put a movie on to watch? I did very little shopping other than online, and am very grateful for Amazon's selection that allowed me to shop from home. When Christmas Day arrived, I felt a bit like Dr. Seuss's Grinch proclaiming:
"It came without ribbons! It came without tags! It came without packages, boxes or bags! (Or Christmas cards from the Borings!) " And he puzzled three hours, till his puzzler was sore. Then the Grinch thought of something he hadn't before! "Maybe Christmas, " he thought, "doesn't come from a store. Maybe Christmas...perhaps...means a little bit more!"
Well I know that Christmas means a whole lot more, and I hope that my Christmas traditions never overshadow the birth of Christ. How comforting it is to know that nothing I do, or don't do, can stop Christmas from coming or minimize its gift to mankind in any way.
It was wonderful to spend time with family. Even our rescued dog, Slapshot, did great being in a new place with new people. I used to worry about how my kids would do with the relatives, and this year I was worrying about how the dog would do. He was very subdued and calm, I suspect due to the Christmas sock he had eaten, but he made a very positive impression on his new extended family members. And so, though I coughed through the Christmas season like Dicken's Tiny Tim, I join him in saying "God Bless Us, Every One!" and may your 2010 be filled with peace and joy.

Saturday, September 19, 2009

To Tell, or Not to Tell?


I've met many parents who are pretty sure their child has AD/HD or some other learning challenge but they are hesitant to make it official by having their child evaluated and diagnosed. The fear that a label may limit their child, be inaccurate, or be used in discriminatory ways is valid. When my son, Josh, was approaching school age I thought about the advantages of private schools with smaller class sizes. Several people suggested that I go ahead and enroll him without telling the school personnel about his AD/HD diagnosis so they couldn't turn him down. That was before we knew he also had an auditory processing disorder. I was assured that once he was enrolled in the school, they couldn't kick him out just because he had a diagnosis and they would be forced to work with him. Wow! For one thing, Josh was pretty easy to pick out of a group as being different than his peers. I'd give it 5 minutes tops before things became unavoidably noticeable. So basically I would have had to keep him out of sight until school had officially started. Then there was the whole idea of the people he would be spending hours with each day being tricked into having a student that they weren't prepared for and apparently didn't feel equipped to deal with in their classroom. That made me feel sorry for Josh and for the teachers, since having someone who was "forced" to work with my child because I had hidden some vital information from them just didn't sit well with me. I loved that boy, and the thought of sending him somewhere that he might not be wanted didn't make sense to me. I had the same dilemma when it came time for Sunday School at church. I didn't want to bias the teachers against Josh by telling them all his struggles, so I coached him on the way there and dropped him off like all the other parents with their children. The Sunday School teachers, bless them all, are volunteers in the church and most don't have training as educators - and for most kids that's just fine. But to do the "drop and run" with a special needs or challenging child is not a good idea, as I came to realize. Every week, the other parents would pick up their children and happily leave. When I came to pick up Josh, I inevitably got pulled to the side and told, "I need to talk to you about Josh." Then I heard, week after week, a full litany of complaints from frustrated and bewildered teachers who were describing things that were not unusual for Josh but were not typical for most children. For example, Josh was not adept at sitting still for long. He was not deliberately disruptive and was never disrespectful, but his need to stand at the table while coloring his page instead of sitting in a chair like everyone else was considered problematic. His sensory issues led him to sit at the back of the group on his carpet square, and everyone else was huddled together and bumping into each other which Josh was carefully trying to avoid. But that meant he wasn't "with" the group because he had made a row of one - just himself! And the list would go on and on until I was finally allowed to leave with my miserable son who knew that somehow just by being who he was he had screwed up again and people were unhappy with him. Those experiences led me to advocate more and be preemptive with anyone I left Josh with for any length of time. When there was a sub or a new Sunday School teacher, I made a point of telling them a bit about Josh and strategies that would help them, and I was careful not to dwell on the negatives. I shared Josh's strengths, too, for I found that if I became negative about my son others felt free to share every little thing they saw as being wrong or weird about him. I was well aware of Josh's struggles and it served no purpose other than to discourage me when others felt the need to complain about him. All this, and he wasn't even doing anything "bad" on purpose! When someone was going on and on about all the things Josh did or did not do, I learned to quietly point out something that he had done right, or I'd share something that Josh had enjoyed learning in their class previously. This seemed to derail some of the negativity some of the time. Just as with our kids, nothing works all of the time but something will work some of the time. We need strategies for working with those who are in a position to care for our children, and hope that something will work some of the time. Whether you are a natural advocate or a reluctant one, if you have a child with a learning difference or special challenges, you must be an advocate unless and until your child one day develops the skills to advocate for himself. In my experience, being deliberate in my advocacy was hard but preferable to what happened when I just waited and hoped things would work out for the best.