Showing posts with label special needs kids. Show all posts
Showing posts with label special needs kids. Show all posts

Monday, December 26, 2011

TWO BROTHERS AND A DOCTOR

Cade hangs with his brother in the waiting room.

You can count on one hand the amount of times I take my kids out of school for reasons other than illness.  Today it may appear I had no good reason to take Cade out of school.
His older brother, Anker, had a doctor appointment with the Pediatric Cardiologist.  Anker doesn’t often do well at doctor appointments.  He equates doctors with poking, prodding, and the need to fight for his life.  Growing anxiety is the way he prepares for the doctor.  The last time we visited Dr. Van Gundy, Anker was too anxious to sit on the doctor’s table.  So, the 6-foot something doctor bent his knees as he sat on the bare floor and invited Anker to lay down beside him.  Anker responded to this gentle giant, and lay on the floor, allowing the doctor to examine his heart.
I was touched by a doctor who understood our son’s increasing anxiety. Try as he may, Anker could not utilize the resources to successfully express his fear.  Dr. Van Gundy communicated compassion to our son, while offering us a great sense of relief. After all, it is no easy task taking a growing boy to intrusive doctor appointments…we have the bruises and bite marks to prove it.


There are two things about Cade which prompted me to take him along to this appointment.  Cade adores his older brother. In the fifteen years of his young life, he has loved his special needs brother with a depth of understanding and strength which blows any observant onlooker away. He gently guides Anker to try the things the O.T. or speech therapist, or optometrist request Anker to do. He models the task, and playfully and patiently invites Anker to follow his lead. Down Syndrome individuals respond well to peer role models, and with gratitude, we have a wonderful role model sharing life beside his brother.  Anker felt relief today, with his brother beside him.
We have experienced many doctors in our special needs journey: doctors who have little sense of compassion, those who lack understanding of our child’s specific needs, and those who are absolutely outstanding.  These outstanding doctors are the ones who speak with compassion as they offer respect and care to our child.  They are acutely aware of the specific special physical needs of our child, and are the very doctors we remain faithful to. Since Cade desires to be a doctor himself, we find great value in exposing him to the characteristics of these outstanding doctors. I knew Cade would offer support to his brother, while gaining an education himself.
Cade sat closely as the nurse examined his brother.  Anker began to shout with anxiety, and Cade talked gently to his brother.  Anker calmed down.  Dr. Van Gundy entered the room and carried on a conversation with Anker,  “You are growing whiskers, aren’t you, Anker?” He took time to visit with our boy. He took time to ask questions, and he gently examined Anker while sitting beside him, this time on the examination table.
Heart problems are prevalent in individuals with Down Syndrome.  Many are born with heart defects and require heart surgery. This is one statistic we have not had to bear.  But, Anker does have a murmur, which we must continue to watch closely. Dr. Van Gundy referred us to a Pulmonary Specialist to rule out sleep apnea issues, and blood tests to check for Leukemia, Diabetes, and thyroid–all medical issues which have a higher occurrence rate in individuals with Down Syndrome.
So, we take the yearly tests, and we continue on with life. We stop for a special milkshake topped with whipped cream and a cherry, then head back to school.  Anker asks to stay home with me–feeling a little too stressed to return to his afternoon classes.  Cade returns to his texts and tests; having gained a little more knowledge from experiencing a life lesson on character with his brother and an extra-ordinary doctor.

BONNIE CHRISTENSEN

Tuesday, September 6, 2011

A NEW DAY: Our Special Need's Summer Vacation - Part 2

Hume Lake 2011 - The Lord is good.

“Yes, boat”, our oldest boy said with a huge grin.  His eyes scanned each of ours as he awaited our response.
A glimmer of hope rose up in me, “Do you want to go on the boat this morning?”
“Yes, boat”, he said a second time.  It was our third day of summer vacation, and our boy with special needs was beginning to drop his guard.  He was slowly adjusting to the change in environment and opening himself up to fun activities.
We barely finished breakfast, but we all intuitively knew to take advantage of the situation.  No one bothered to put on their bathing suits or sandals, instead we scurried off to the boat house.  This time we avoided the creaky wooden dock and the rowboat which rocked so much it shook his footing.   I stopped to pick up paddles and life jackets while the boys walked straight to the kayaks—the red ones, because red is AJ’s favorite color.  It made him equally happy to adorn the red life jacket.
AJ cautiously walked through the muddy path, weaving in between the other boats, then awkwardly swung his leg into the kayak.  Dad held the boat steady while brother helped AJ sit down.  The kayak was a good choice.  He was able to sit securely on stable land while his Dad gently slipped the kayak into the lake.
The rest of us stood on paddle boards and glided alongside the kayak.  He was not protesting with the anxiety he displayed yesterday.  Quietly grunting to express his discomfort, he suddenly changed his tune. “Yea!” he yelled and then applauded his own accomplishment.   I dug my paddle through the water as my toes dug into the board.  Our other two boys stood beside me gliding through the lake on their own boards.
My youngest boy teased me and reached his paddle out to nudge my board.  My feet changed positions to regain balance, but down I went.  I crashed into the water with my skirt flowing up around me.  Thankfully, most of the campers were still eating breakfast and there were no other boaters on the lake.  With little grace, I crawled and slipped my way back on the board.  What a great morning.  We floated and laughed and enjoyed each other for a couple of hours.
This is a rare occasion.  Do you know how often some of us special needs families are able to enjoy adventures together?  Often times either my husband or I hang out in the hotel room watching Lion King with AJ while the other parent takes the siblings out for fun.  What a gift we experienced this morning; two parents together with all of our children enjoying the lake.
Carefree in the kayak
We pulled our boards and the red kayak ashore after a great morning of water fun.  The boys stripped off their life jackets when AJ requested, “more boat ride”.  So, out went he and his brother on a second adventure.  This time he was done after 10 minutes, but he was able to build one success upon a previous success.  The praise and the high fives and the gummy bears were flourished upon our boy for the happy choices he made.
The family was encouraged with progress while the heart gives credit and gratitude to our Lord. Thank you Jesus, for a carefree spirit in our boy today.  Please give us more. 
I’m going to pray this prayer relentlessly.
AJ enjoyed many moments of relaxation on vacation

BONNIE J. CHRISTENSEN


Monday, August 29, 2011

SPECIAL NEEDS, STRESS, AND OUR SUMMER VACATION



Slumped on the picnic bench, I sit disappointed as I listen  to our son say, “No” for the umpteenth time.  It is the end of summer break and we are on our one and only family vacation.  Our oldest son, who has special needs, is filled with stress and anxiety this morning.  “No” is the limited word choice he uses to express his discomfort.



We apply our behavior plan, but the negative behavior looms.  The rest of the family continues discussing the day’s plans as we sit around the picnic table.  My mind wanders away from the conversation, wondering if there are other tools we could use to coax our boy along.  Sinking my chin into the palm of my hand, I watch him as he eats and I begin to pray, “Jesus, please help him be carefree”.



We couldn’t have picked a more relaxing, stress-free vacation place.  Regardless of the calm lake and lazy schedule, our boy was stressing over straws for his cup, climbing into a rowboat or walking up a small row of stairs.  The anxious behaviors interfere with his ability to enjoy new experiences and relationships.



Our family of five responds to his needs like second nature.  We take paths of least resistance; avoiding stairs and carrying straws in our bag.  We plan to ignore negative responses; trusting the lack of attention will deflate some behaviors.  And we carry a “tool box” of high fives, praise and gummy bears for his great behavior choices.

Brother encourages brother on stairs
We have come to expect new situations will often create anxiety in our son.  A new place to sleep, a change in schedule, and crowds of people can throw off a normally delightful child.  This is the life of a special needs family.  There are times we respond to his behavior with our own erupting stress. More often we take deep breaths and dig deep inside ourselves to persevere and love and laugh, and sometimes cry, (speaking of myself).



Most of all, I pray.  Try as I may to be equipped with effective survival tools to empower my family, ultimately I have very little control.  I release our boy to One who loves deeper.  As everyone finishes their breakfast I silently pray, “Lord thank you for giving us tools.  Thank you for giving me a kind husband and compassionate sons.  But, I pray for a carefree heart in our boy.  He can’t pray it for himself.  I pray You’d work your Spirit within our boy…to relieve him of his anxieties…give him joy and rest.  Only Your Spirit can do that, Lord.  Do a mighty work.”



I’m going to pray this prayer relentlessly.



BONNIE J. CHRISTENSEN