I have gained so much knowledge
after interviewing two teachers who work in Special Education. I explained that
my topic was autism, and they both offered plenty of information.
The first teacher who I interviewed
works with 3 and 4 year old children who have autism and works in a
self-contained setting. She believes that there are several issues in autism
which include diets, sensory needs, education, least restrictive environments(LRE),
communication, and transitioning.
She said that one of the
biggest problems she encounters is that the parents of her students do not
understand or remain consistent with the way that she approaches their child's
behaviors at school. As a teacher, she tries to educate the parents as much as she
can, but the district does not allow them to have home programs in which they
can help them in the home setting.
Another major issue that the first teacher
mentioned is that the clinic team that assesses and places students does not
seem to have a good grasp on what her classroom is all about. She actually has
been getting some students that could have benefited from a less restricted
environment but she cannot tell a parent that when a child enters her room. The
only thing she can do is bump up their skills and send them on to an early
childhood class the next year.
The first teacher who I interviewed believes that the LRE is most
important and concerns her. Students are being diagnosed with autism more and
more, and she’s not quite sure they need to be diagnosed so early unless they
are not getting early intervention services without it. When a student turns 3
it's important that the clinic team knows what goes on in each classroom in
order to determine the best placement for that student. The teacher has spoken to the administrator
about having the clinic team observe in her room so they get a better idea of
what her classroom entails so that LRE is discussed and students are placed
appropriately
The second teacher who I interviewed
works with 5th-8th graders who have autism. She feels
that the most important thing for people to remember about autism is that there is not a
cure to it, but those affected with Autism can grow, improve and progress. She
understands that not all students will progress the same. Not all students will talk or be able to move
out on their own. She feels that one of
the biggest issues with autism is the misconceptions. She thinks that it is sad
that parents think that vaccines cause Autism.
There is no proof of this and no study to confirm this. It is important for doctors to educate their
patients and parents of children on this misconception and the importance of
vaccinations, especially in our modern, global society in which we exist. Next, she thinks that it is essential that
parents understand the necessity of getting their child into therapy or school
as soon as they receive a diagnosis for Autism.
It is essential that all parents get their children screened at two or
three years old to help catch any disabilities.
Finally, she thinks that one of the most important topics people need to
know more about and be educated greatly on is how to deal with behaviors. She believes that parents need to be trained
on this, work hand in hand with counselors, social workers, teachers, anyone on
their child’s team, to create a cohesive and structured behavioral plan to help
the child learn what are appropriate and acceptable behaviors and what are
not.
The second teacher feels that some of
the biggest issues are helping parents understand how to deal with Autism, how
to deal with behaviors, and how to find help for their children. There are so many quacks and “heal Autism”
gimmicks out there, that parents do not know which way to turn. She also believes that parents need more help
on knowing how to deal with negative behaviors.
More trainings should be offered and insurance should help cover any
therapeutic needs for students with Autism.
There are so many parents that fight for their insurance to cover
things. And it is difficult and time
consuming to receive free help or there are many institutions that put parents
on lengthy (years and years) waiting lists to receive any free help.
.
These
interviews helped me tremendously! I already knew which topic I wanted to chose
because I am so passionate about it. However, there is so much more that I
would like to learn before I put an advocacy plan in place. The first and
foremost thing that I want to focus on is the assessment and placement process.
This is extremely important, not only for the children, but the teachers as
well. It’s only fair to place the child in the correct classroom so they can
receive the proper education. Both teachers seemed very concerned with making
sure the parents receive the proper trainings and gain knowledge about autism.
The other issue is funding. Without the proper funding, it is hard for parents
to get the help that they deserve.
After interviewing both teachers, I’ve
decided to focus my paper on autism. Three additional topics are Assessing/Placement, Family Resources/Educating Parents, and Funding.
Questions I have for my colleagues
related to this area of interest are:
Does anyone work at school that assesses
and places children? If so, how do you feel their accuracy is? Do you feel that
an hour evaluation is long enough to determine the fate of your child?
Does anyone know of any good resources
for parents of children with autism?
Where could these parents go for help
with their home life? How can they reciev additional services if they can not
afford it?