Monday, September 14, 2015

Social Integration 

How we promote the social integration of students with exceptional learning needs can depend on our role in the school setting.  As a nurse in the school setting I have the opportunity to spend time in the classroom with students and speaking to parents outside the classroom on a routine basis.  Some children with ELN have continuous medical needs.  Because of this, I speak to parents often.  Not only do parents share medical needs, they share thoughts and feelings that every parent has regarding their child making friends.  My background is pediatric nursing for a children’s hospital.  Family centered care has always been a focus for me as a nurse.  Pediatric nurses must consider the needs of the entire family unit in order to provide the best care.  Family centered care definitely is a must when a child with ELN enters school.  As Jimenez and Graf state in Education For All: Critical Issues in the Education of Children and Youth with Disabilities, “families are the stable and constant force in a young child’s life and therefore play a critical role in the educational process.”(pg.44). 


I have found that outward appearances of students with ELN can sometimes be off putting to students and parents of typical peers.  By demystifying some the outward appearances of students with ELN, barriers can be removed to promote social integration.  Finding common ground between students and families helps to not only promote social integration, but helps to form friendships, bonds and a support systems.  In my school district we have 6 elementary schools.  Children often go to school, kindergarten through grade 5, with the same group of children year after year.  I can sometimes take down some barriers of social integration, through education.  I try to educate students when children immediately enter school.  I want to address differences and similarities with the children in the classroom and their parents outside the classroom.  When we have a student with ELN that may “look” or “act” differently, I may do education on a special disability or chronic illness.  I first speak with the family and teacher of the student with ELN for permission to talk about how their child may look a little different than other children.  My goal is to educate the students and families so there is no fear or exclusion of the student with ELN.  I like for students to be aware of needs and feelings of each other.  For instance, we have a new kindergartener with a trach and is in also in a wheelchair.  I spoke to the class about his “special band” around his neck and his wheelchair and why he needs them.  We also go around the room and ask what makes each student happy.  When it was this particular students turn, he shared that he likes to play with friends.  Since he cannot speak, he points to the friends picture on his wheel chair tray.  This opens the dialog that he likes to play with friends, just like everyone else does, but he just can’t say it with words.  I try to take away the fear of how outward appearances may be different, but on the inside we all have feelings.  We also send home information to families in the backpack.  This information is for family dialog at home.  If parents have questions, they are welcome to contact me. 

3 comments:

  1. Cindy, I agree that educating a class about a student who may “look a little differently” can definitely help demystify any questions or concerns students may have. In the previous school I worked at, we had a student with neurofibromatosis that also had a trach. He was an exceptionally bright student with an A+ personality. He started at my school when he was in kindergarten and last year when I left he was in the 8th grade. Previous to that he had gone to the integrated preschool at Fairhaven. The student was very comfortable responding to students who stared at him. One day while he was in the clinic, a younger student asked him what that hole in his neck was. He responded, “Don’t worry, I have it to help me breath”! He was very comfortable with his image and I attribute this to the education of his disability to the students at the very beginning. He also had wonderful attentive parents who helped foster his very independent attitude, (even though he wasn’t able to be physically independent. He had many friends and it was so endearing to see the young students in his class attend to him when he needed help.

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  2. Cindy, I could t agree more! Teaching our children to not "judge a book by its cover" at a young age is wonderful! I am a firm believer that humanity is uneasy about the unknown, and educationist our children at a young age about the "unknown" of different health requirements will eliminate some of the bullying that may occur later. I also LOVE that you sent home information to the families, allowing the families to teach acceptance and awareness to their children and staying connected to school. Awesome job!

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  3. I love the idea of education not just the parents but the students also on specific disabilities and allowing them to better understand why a child might be “different”. I think the most important lesson would be getting them to realize that they’re really not that different after all. I agree with you that communication with the family is important in this process. A suggestion for following through with this would be to use bibliotherapy. Bibliotherapy can often be combined with writing in order to promote social and emotional wellbeing!

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