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SPECIAL NEEDS, SPECIAL LIFE

Welcome to a mom's blog about life with her special needs daughter, Angela Maria. This is a unique blog for you to explore and hopefully gain insights into living with and caring for a child whose needs go way beyond normal. My name is Carol and I'm ready to share our story of 43 plus years in the hope that it will help you. 
 

Angie's life story is really a huge part of my own story and through the experience of caring for her, I have gained a much better understanding and greater insight into how to live joyfully and happily in the moment while at the same time coping with a great number of challenges. I'm delighted to have found a platform where I can post my story and share my passions, thoughts and experiences with you, my loyal readers. I'm writing this blog with the help and support of my sons and family. Read on, and enjoy. Feel free to ask question too.

Newer post Are at the the top so if it's your first time here start At Angie's STory

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WHY NOT ME..

  • Carol Weidner
  • Dec 1, 2018
  • 2 min read


12/5/18 The next step in treatment became a series of castings. One therapist would position her feet as close to neutral as possible with their hands, while the other one padded and wrapped her feet with plaster cast. The casts were changed regularly to prevent pressure sores and to gradually stretch her muscles. Through all this Angie was a trooper. She didn’t cry. She watched. I hoped. When they removed the casts, her feet pulled in as before. She went through series casting for quite a long time, but in the end, her doctor and therapists decided that the only solution was surgery. So off we went to see the orthopedic surgeon. Meanwhile, my parents offered continual support in day to day activities. My friends and family also supported us by inviting John to play groups while I took Angie to therapy and UCP Preschool. One day a week I took John with me when I took Angie to preschool because the hospital in Cincinnati is very near the Cincinnati Zoo. John and I wondered around the zoo as often as possible (We had a yearly pass!). Later, he used to tell people that he went to the zoo so often that he knew all the animals by their first names. We were happy. I had support from my parents and extended family, my church and my hospital friends. In addition, a group of mothers from the hospital had formed an organization called “Mothers of Special Children.” Mothers of Special Children was wonderful. It was the place we could talk about our “special needs” kids with people who really understood our situation. It was the place where I got to meet parents of children who were older. As a group, we planned fun events for our children and for our whole families, we had fund raisers for projects we cared about, and we had small gatherings at people’s homes where we could chat informally. I remember one such meeting where our hostess shared the story of her ten or eleven-year-old son’s grave condition. He had a condition where he would die before he became a teenager. This story was heartbreaking, but from her sharing, we all had the occasion to discuss ways to cope and ways to think differently about parenting our kids. I’ll never forget this day because it was here that I was challenged to stop asking, “Why me?” and start asking “Why not me?”
 
 
 

1件のコメント


gretchenmbohman
2018年12月13日

What an incredible read. Thank you for being transparent and raw in sharing your family story. I cannot wait to read more!

いいね!
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