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.
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.
ReplyDeleteCindy, 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!
ReplyDeleteI 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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