Guest guest Posted October 3, 2003 Report Share Posted October 3, 2003 Hi, I read this today and thought it may be encouraging to some of you too. Though it is talking about cerebral palsy, I believe it applies to all of our children too. Have a blessed day! Melony My Struggle . . . My Blessing? By Suzanne Keffer, Writer, Creative Ministries As a child born with cerebral palsy (CP), I questioned God many times. Born nine weeks early, I weighed only three pounds and four ounces. My dad affectionately referred to my lowest weight of two pounds, twelve ounces as just eight sticks of butter, " and my mom dressed me in doll clothes for two months. However, it would be several years before they knew I had a problem. The fact that I failed to walk until two-and-a-half signaled the first warning. The next alarm flashed when I walked only on my toes. I can still hear my mother's voice echoing, " Put your heels down. " But no matter how hard I tried, I could not walk like the other kids. I longed to run the bases at recess, to flip off the diving board, or just to climb the stairs at school without losing my balance and falling down. Most of all, I begged God to let me walk flat-footed so that the other children would not make fun of me. God's Word said He loved me and promised to bless me, so I knew that He could cure my cerebral palsy. Surely, if God loved me, He would grant my prayer. At night, I knelt at the side of my bed asking God once again to take away my CP. And in the morning, I climbed onto the bus feeling the cruel stares pierce through me another time. As a first-grader, I did not understand how my lack of oxygen at birth deserved Brad's insults at school. He performed his daily routine at lunch in the school cafeteria, walking high on his toes mimicking, " Look at me, I'm Suzanne. " And everyone did look, including me. I wouldn't let them see my tears. I only showed those to my mother. In Psalm 56:8, the Lord reminded me that He kept my tears in His bottle. And I said, I know, but why haven't you granted my prayer? " Every day, my mom encouraged me to believe God's Word over Brad's taunts. Though she didn't quote Psalm 139, she often showed me that I was " fearfully and wonderfully made. " I still remember the collection of brightly colored shoelaces she bought me when I had to wear a dreadful pair of black and white corrective shoes with steel-plated soles (which eventually snapped). My Dad never let me use my condition as an excuse. He expected me to do my best and saw beyond my limitations, exhorting me to develop the gifts God had given me. My older brother valued me, helping me onto the bus and scowling at Brad all the way to his seat. As I grew physically, the Lord also matured me spiritually. Through my family and His Word, He abundantly proved Psalm 84:11, " No good thing does He withhold from those who walk uprightly. " (NASB) He taught me how to deeply depend on Him and to value how He made me rather than how I walked. I learned at a young age to let my identity rest on Christ rather than on my abilities or disabilities. And Brad's ridicule gave me the gift of compassion, a treasure I might never have received without him. In the sixth grade, God brought me another good thing. I had never heard of Texas ish Rite Hospital for Children, but they had heard of cerebral palsy. These volunteer doctors had perfected a procedure to lengthen Achilles tendons and hamstrings by partially severing them. Just as a nicked rubber band stretches to a longer length, my muscles would lengthen and rebuild themselves when they were cut. At my pre-op appointment, the smell of fresh popcorn filled the waiting room as the spinning spokes of bicycles whirred above my head. Two prosthetic-wearing aviators pedaled a blimp furiously through the sky. I wondered if I had missed school to go to the hospital or the fair. Just then a clown with shoes uglier than mine honked his horn at me, making me laugh. Children with metal-braced legs creaked stiffly toward the pink-haired clown to get a rainbow balloon. A five-year-old boy in a wheelchair clapped his hands in delight as the circus mime skipped toward him. Though I could not understand his slurred words, his smile said it all. A little girl with plaster legs rolled herself toward me. " My name's Jenn. Do you want some popcorn? " " Sure, " I answered. " Do they hurt? " " My legs? Sometimes, but this surgery hurt way less than the other four. I only have two more to go. " " The other four. Two more to go? " I thought, trying to hide my shock. " How many do you have to have? " she asked. " One. " " Wow, you're really lucky. You'll get to go back to regular school in no time. " When I returned to Sam Houston Elementary, I felt like a poster child with two full-length plaster casts and crutches. As I watched my friends play kickball, I wondered if Jenn was getting to play outside that day. My four-legged status certainly gave Brad more material for his daily routine. But when I remembered Jenn, his words didn't sting as much as they had before. On my last post-op visit to the popcorn fair nearly two months later, the metal saw reminded me of a supersonic pizza cutter as it smoked its way through my plaster legs. The powder haze irritated my eyes. The air smelled electrical-the way it did the first time Dad turned on the heat each winter. I had grown to depend on those plaster shells that lay lifeless on the floor My own legs felt frail without their plaster shields. Still propped on the crutches, I feebly took my first new steps. " Left crutch, right leg, right crutch, left leg. " As the weeks passed, I mastered bipedal walking again. But this time, I heel walked " rather than " toe walked. " Twenty years later, I still walk with an irregular gait. Now I have a hard time even standing on my toes. With my lack of balance and coordination, I would flunk a sobriety test sober. However, I consider myself fortunate to have had cerebral palsy. In his sovereignty, God used a birth defect to bless me. Through cerebral palsy, He taught me dependence upon Him, identity in Him, and compassion through Him. Most importantly, He used my CP to show me how to think of others rather than focus on myself. I thank my Father often that in His grace, He allowed me to be a " toe walker " for the first 12 years of my life. I also thank Him that He never took away my weakness completely because the day-to-day dealing with it drives me to rely on Him. My gratitude flows from my certainty of God's promise, " No good thing will He withhold from those who walk uprightly. " (Ps. 84:11 NASB) Your Child . . . Your Calling? If God has given you a child with special needs, you may find yourself asking why or praying for a miraculous cure. If the answers you desire don't come and the challenges of caring for your son or daughter continue, remember that the God of the universe has entrusted you with the amazing task of embracing a child that many people would reject. While it's not the baseball games or ballet recitals that you imagined, it is a divine invitation to nurture a " fearfully and wonderfully made " being. She may never hear your voice or say your name. He may thrash every time you hold him. She may have a four-year-old mind in a twenty-four-year-old body. They are God's creations. You are the steward He chose to care for the precious soul inside an imperfect body. No matter the degree of your child's disability, treat him or her with CARE: Challenge him or her to excel. Whether your child faces minor challenges or major obstacles, always stimulate his or her development. While distinguishing between red and blue or drinking through a straw may seem like a small victory to you, the confidence your child will gain is immeasurable. Even if he or she never masters a task, the time spent with you and others will benefit him or her. Affirm his or her value. Like all children, kids with special needs yearn to know their worth. When your child interacts with people like Brad who don't understand her condition, she may question her value. Be prepared to talk frankly about her developmental differences. Teach him to tell others about it when they ask. Comfort him when he hurts. Remind her that God made her. Offer him the opportunity to learn forgiveness as he faces others' jeers. Realize his or her limitations without limiting his or her potential. While you may need to assist your child in many areas, don't allow your help to become a hindrance to his or her independence. Guide him with as much freedom as possible. By empowering your child to do some things on her own, you give her self-assurance. If you think he might fail, let him try. If it takes her a little longer to dress herself, get up earlier. If her clothes don't match, don't worry about it. Encourage him or her to interact with peers and people in the community. Don t isolate your child from others in an effort to protect him or her. She needs to socialize, and you need outside support. Let her get to know other children-both kids with typical development and kids with special needs. Ask older kids or adult friends you trust to spend time with him. He should learn to relate to people outside his family. Cultivate an environment that will allow your child to bloom socially. When he stutters, someone may snicker. When she asks for help up the stairs, the first person may say " No. But the next " Yes " could be the new friend she never would have met if it weren't for the first " No. " When your child's skills do not allow him to function on his own, consider assisted care. As he matures, a special needs daycare can provide a social outlet. If she wants to live in a group home at eighteen, don't hold her back. If you CARE for your child well, your son or daughter will likely look beyond his or her needs to see the special kid you see. Her " Reasons I'm Special List " will include her Maker, family, friends, abilities, and challenges. Though your ideal family photograph probably didn't include a child with special needs, God's perfect portrait did. Just because your picture has changed, don't forget that God has given you a good thing. Desire the best for this soul that He placed in your life. You may never watch him hit a homer or see her dance Swan Lake, but you can focus on realizing new dreams with the extraordinary kid God has entrusted to you. .. Quote Link to comment Share on other sites More sharing options...
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