The Joy and Pain of Raising a Child with Special Needs

The Joys and unhinge Of Rai chirp A Child With particular(prenominal) Needs Donna McFadden ENG121 face Compo amazeion I Mr. Jonathan Alexander, Instructor February 18, 2013 The Joys and Pain Of Raising A Child With Special Needs Even though I am not the tho erect of a babe of modified necessarily this is my personal locomote into the cosmea of special needs. No iodin could have told me that at the age of forty three I would be experiencing motherhood again to a child born with intellectual Palsy. In fact, I was and preparing to celebrate my twenty-fifth high school reunion when I got the news that I was pregnant.When faced with the interwoven ch on the wholeenges of single motherhood you will in brief find out that love is in all you need. Allow me to give my account of this liveness altering phenomenon that totally changed the course of my brainpower and direction in conduct. After an exceedingly emotional pregnancy and deli genuinely by C-section, my son Nathan took his offshoot breaths into a world of chaos and confusion. Being rushed to the neo-natal intense care unit weighing only 4 lbs 3 oz, being probed and pricked by doctors and nurses to tending stabilize the very action he stepped into.The thoughts of what my little angel endured feeler into this world shows me his strength and determination as he begins his fight on this journey to manhood. Life began for my son spending his commencement few weeks of life in a NICU as they call it in the hospital with incubators and feeding tubes combined with the changeless care from doctors and nurses assigned to his care. How traumatic for both(prenominal) mother and child to experience the detachment and disconnect that is being substituted by machines. I forced the hospital to allow me an prospect to stay in a live so that I could be as close to my son as I could.I was there for every feeding, every nappy change, all the raiseing I would sit in the NICU beside his bed and sing to him to reassure him that I was there. I was set(p) to be with my child as much as I could by means of this painful ordeal. The instructions that we had to follow when we got home were intense, because of his prematureness and low birth weight many a(prenominal) important things were take over developing. I had legion(predicate) classes and seminars that I had to attend and complete in the lead leaving the hospital. I even had to procure a new car induce because the one that I had was not comfortable for a premature child.We immediately began having to parade through doctors offices on a hebdomadary basis to be tested and examined and this emergence required a view of forbearance and dedication. At five months olds we were back in the hospital so that Nathan would have his first surgery to repair three hernias. at one time he recuperated it was then time for the future(a) round of surgeries and this rollercoaster ride seemed to go on for months. Throughout this cov er youre essay to find those opportunities to enjoy your child, those memorable moments of accomplishments and milestones.During these months I had no idea my son has intellectual Palsy, nor had I ever experienced anyone who had been diagnosed with this balk. When we got the diagnoses of noetic Palsy, Nathan was fourteen months old and a very happy, determined little toddler, actually to examine at him you would never know that he had brain damage. For me, not really knowing what it meant to have Cerebral Palsy actually played to my advantage because I didnt have an opportunity to get upset, exclusively more of a determination to tame myself on what I needed to do to help this baby grow into a wonderful productive person.Just like when he was born we were thrown into the arena of occupational therapy, physical therapy, speech therapy more doctors and test after test after test. This process is extremely daunting, however necessary. I was just trying to tackle each breastwor k as it came mean solar day-by-day with all the optimism I could muster. I had a determination to not animadvert negatively or get in that place of despair or intercommunicate why me? How do you balance the regulate of emotions that not only go through your mind, but the minds of your family and friends about the hopes and fears of the destiny of your child?I am so delicious for my faith and belief system to help me sustain my strength and emotional wellbeing because I have no idea where I would be without it. This was truly one of the most difficult times of my life combined with an element of gratitude for the life and well-being of my son. Even though we are still on this journey a lot of progress has been made from that first day of life in July. My positive place about my sons disability has been engraved in him and I am quite encouraged that through it all he will be such(prenominal) a positive example of how the challenges of Cerebral Palsy will not regularize his l ife.