The education of a special needs child begins at birth. First and foremost, a baby is a baby, no matter what their health status is. All babies need love and attention for proper brain stimulation. Read to your baby. Sing songs and recite nursery rhymes. But most important, give a lot of hugs, kisses, and "I love yous."
In 2004 the Individuals with Disabilities Education Improvement Act or IDEA was passed. It basically ensures that all children, regardless of their disability have the right to a free public education including early intervention. If you think that your child might require special education, you can request that your child be evaluated by your state's early intervention program. If your child is delayed 40% in one area or delayed 20% in two areas, he or she will qualify for services. You and the early intervention services will then create what is known as an Individualized Family Service Plan, or IFSP. An IFSP is basically a road map that shows where your child is and where you would like them to go. The IFSP will include goals for your child to reach, what type of services will be needed in order to reach these goals (physical therapy, speech therapy, etc...), who will be providing these services, how frequently will these services be provided, and where these services will take place. The IFSP is reviewed every year to make sure that the child is on track and if services need to be added or dropped.
At the age of three, the child will go through transition. Basically they will move from early intervention with an IFSP to public special education with an Individualized Education Program, or IEP. The IEP will include new goals for the child and how they will be met. The IEP is reviewed every year. Those present at the IEP meeting may include the parents, a general education teacher, a special education teacher, an administrator of the school, specialists in your child's disability (invited by you or the school), guidance councilors, and, if you wish, your child.
When making or reviewing your child's IEP, it might be a good idea to bring along a little packet explaining who your child is and what you think is the best direction for your child's education. Frequently the general education teacher and administrators at the meeting know nothing about your child. The only thing they know is that they have had their schedule interrupted to attend an IEP meeting about a child that they will probably never see in a classroom setting (the general education teacher does not have to be a teacher that your child has). Having a little booklet of information about your child gives them a story and a reason to care. You can include pictures, art work that your child has made, or even copies of their baby book pages. Let them know how wonderful your child is and how hard you are working to make sure that they are getting the best education possible.
If you ever feel that your child's goals are not being met, you have the right to call the administrators and remind them of IEP and its goals and how you think that the problem might be fixed. Not having enough money is not an excuse that the schools can use in defense if an IEP goal is not being met. They will have to find a way.
Making sure that a special needs child has the education that they deserve is up to the parent. You are your child's best advocate. Make sure that you know as much about your child's condition as possible and take the time to review your child's rights as stated in IDEA. You are your child's best hope for a bright academic future.
Published by MD Sparks
Native Tennessean with a passion for writing. View profile
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- Make sure that your doctor sends in a referral to your state's early intervention program.
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2 Comments
Post a CommentGreat article. I know you are right that the more involved the parents the better care the child will receive. My parents proved that with my little sister.
Thanks for this article. Both of my brothers were born with learning disabilities, but they received special education from a very young age.
Sophie