Showing posts with label special education. Show all posts
Showing posts with label special education. Show all posts

Tuesday, September 23, 2014

School, Teachers and the Special Needs Child


This day certainly seemed like a better day in theory than it is turning out to be, however.....maybe we are just getting all the yucky parts out of the way early and the rest of the day will be bright and sunny! Yeah....I don't make a very good Pollyanna do I?!

I really wasn't sure what I was going to post about today as David is doing pretty well. We have got his seizure meds adjusted and he seems to be in a better mood now. We also have his Physical Therapy(PT) underway and he is doing very very well with it. There is really not much new here in Davidtopia to discuss, and that is a good thing. Therefore I was feeling at a bit of a blog loss....when I got a message from a lady telling me about her young son who among other things has seizures and she is having issues with a teacher taking this seriously. My blog just wrote itself at this point.

Not all special education teachers are created equally!!!! If you are a sped parent.....please commit this to memory. In the course of your child's education, you will have teachers that are simply amazing and teachers that you wonder how or why they ever even became teachers. David has had both and honestly and fairly, he has had more good than bad, however.....the bad ones do seem to overshadow the good ones. Sad...but true!

When your sped child starts into school, they usually will start early. David was started at 3 years old into the Early Childhood Education program at our school. At the time, they had mixed classes with sped kids and gen ed kids. The program was amazing because the teacher behind it was amazing. The belief was that if you mixed the kids early, gen ed kids would grow up around sped kids and there would be a greater understanding of disability for the gen ed kids. It worked as kids have always been very accepting of David and this is shone in their kindness and gentleness towards him even 11 years later.

Any classroom is only as good as the staff!!!! Something else that parents must commit to memory. Sped classrooms are made up of a teacher, para's and support staff such as PT, Occupational Therapy (OT), Speech and sometimes even a nurse depending on the physical severity of the kids in the room. If this team doesn't work together as a well oiled machine and have the best interest of the kids in mind, then this classroom is a fail right off the bat. Usually the teacher is leader and sets the stage for how efficiently the classroom is run. Uninvolved, under educated or out of their element teachers can make for a very long year for the other staff and a very unhappy year for the students....not to mention us parents.

Sped kids are not easy and even in a small class room of possibly 8 or less kids, there can be a multitude of different diagnosis's, personalities and physical issues which all fall under the head of special education and quite often they fall under one teacher. There can be higher functioning kids, lower functioning kids, seizure kids and kids with oxygen and feeding tubes all in the same class room. This is why para's are so important. They are the constant companion of these kids and it is their responsibility to know when that kid is just acting out or if there is something really wrong, but in order for this to happen, the teacher has to make sure that the staff is properly trained. The only way this can happen is if the teacher makes it his/her business to know the kids inside and out and has a thorough background on each child. How does this happen? By listening to the parent!!!!

Granted, I know for every great sped teacher, there are always those parents who live in denial of their child's diagnosis, refuse to cooperate or simply are too overwhelmed to deal with it all. However, for every sped parent who is involved and fighting for their child's best interest, there is at least a handful of teachers, para's and specialty therapist who never should ever  be in a room with a sped child, let alone work with them. Because of this, sped parents have to be ever vigilant and always ready to fight for their child's best interest.

In David's 11 years in school, I have had several fights over staff and trust me, the schools do not like to back down. It takes work, research and a willingness to see the situation to the end, but usually....the best interest of the child wins out because I can wear someone down if need be. David will always come first and his best interest will always be served and quite honestly, from the beginning I was told that I would always be David's voice and his biggest advocate. I was told that it was not only my right but also my duty to stand up for David and to fight for him when his needs were not being met, he was not being treated right or his health was at risk. I took this very seriously and because of this, I am not the best liked parent in the district, but they know my concerns are never frivolous and if they are hearing from me, then there is a "real" problem that will be fixed. Even in my small town, I am not interested in being liked by the school district and staff, I am interested in my sons needs being served and I will do whatever that takes.

If you are a beginner sped parent, prepare yourself. You have to be involved with your child's education. Make it your business to know everyone in your child's classroom and on their team. Make sure your concerns are listened to and if your child has a feeding tube, seizures or other issues, you personally need to educate the staff on how to care for your child. They may have your child in their classroom, but absolutely no one knows your child better than you do. By setting this standard from the beginning, you help to promote the best school environment for your child that is possible. You also give the staff a subtle reminder that you are a constant presence in your child's life and that little gets by you so if something isn't right......you will both know it and act upon it. Also, show up at your child's yearly IEP meetings and find your voice. You may have been a live and let live kind of non-confrontational sort of person before you had this child, but those days are gone. You need to give your child and his/her diagnosis and condition a voice. Without it, they may not be getting what they deserve in school nor even what they need. As their parent....you owe them the very best and sometimes that requires going to the mat for them.

I suggest that from the beginning, you get an advocate for your child and your family. An advocate can be a tremendous source of information for programs and assistance to help with your child's development and if you do have to battle your way through situations, an advocate should always be on hand. Davids advocate is through Rainbows United, but every town and state should have a Developmental Disability Organization in which sped kids can sign up and go through, throughout their lives. Early acceptance into these programs can assure space for them in programs later in life as there are years worth of waiting lists to get into some groups, programs and even funding.

Special needs kids don't come with a owners manual. Each kid is different as are their personalities and their diagnosis's. They require more attention, more care and parents that aren't afraid to fight for them in any situation necessary. While the life of a sped kid is not easy, the life of a sped parent can also be a bit challenging. However, at the end of the day.....I wouldn't trade a minute of David's life or what he has brought to mine, for an easier, less confrontational road. David is amazing and after all......he is the Incredible Mr. David! And there just ain't no topping that!!!

Wednesday, September 10, 2014

An Update and An Opinion


Yes, once again I am painfully aware that it is Wednesday and I am just as painfully aware that I have no projects or even real accomplishments to show for this week......unless of course you consider going through 3/4 of a tank of gas running around to different appointments an accomplishment. If that's the case then I should get a gold star for my efforts!!!! However, since I missed blogging about David yesterday because I was running and all, I figured you all might like to hear about him instead of how many gallons of gas I used in the last two days! Your welcome!

Yesterday was David's first official physical therapy appointment. To say I am over the moon with this new therapist would be an understatement. This girl is very good as David let her work with him the entire time without getting upset at all. There are two definite reasons for this. The first one is she is a little tiny girl who is just gorgeous. Definitely Davids type. And the second and probably most important reason he behaved was because she knows how to distract kids from the task at hand. She played on Davids love of balloons and gave him one of those really thick balloons with the rubber band attached. He played with that the entire time as she stretched him and manipulated his muscles. She and the entire staff were also huge on praise and as he walked with his walker through the gym. The other therapist and office staff came out to high five him and tell him how great he was doing. It was the push he needed to continue. Yes, David does now, and always has, worked well for praise.......and candy!

After the PT thoroughly checked out his strengths and weaknesses (and there are still a great many weaknesses), she came up with a plan. This plan she assured me would ensure that his weakness would be improved upon greatly. Under this plan, David will be seeing her twice a week and then seeing the swim therapist once a week. With all of that and horseback riding therapy (HIPPO therapy) too, we should be seeing some great changes in David fairly soon. I am excited....not just for the change, but also for how he relates to this therapist. I feel like we are finally headed in the right direction!

As if that wasn't amazing enough, before his therapy yesterday, David had his yearly IEP. While I can't tell you what those letters stand for, I can tell you that it is a meeting with myself and all involved with him at school. It is to check on past goals and set up new goals for David scholastically. It covers his basic educational needs, while including all of his therapies. If you remember, last year I spent the year very unhappy with school, but this year, it is a night and day difference. There are many new faces in the mix and some fresh ideas balanced by some impressive experienced ones. I am so pleased with all I have heard and seen at school this year and although David is still adjusting to getting back in the swing of things.....he is also thriving. I am a happy momma so far!!!

So we are all moving forward. Now if I can just keep that nasty virus that is going around away from him. THAT has ER/hospital visit written all over it. I did tell the teacher yesterday that if kids start getting sick with this, I will be keeping David home for a few days to avoid contact. I know I can't protect him from everything, but from this wheezing nightmare.....I will do my best.

Finally, I would like to say a word about the young special needs child who was trying to be a part and participate in the ALS Ice Bucket Challenge. Some other kids, as a prank doused the child with urine and feces instead of ice. My question is....why? Why would someone think that was funny to do to anyone, let alone an autistic child? This young man was 15 years old and he thought he was doing something good and being a part of something special. Instead, he was deliberately humiliated, I'm sure embarrassed and bottom line....bullied.

It is my understanding that the kids responsible have been identified, as celebrities such as Drew Carey and Jenny McCarthy (who has an autistic child) put their resources to work to help find the offenders. So should these kids be punished? Should charges be filed against them? Here's my thoughts...... The offenders should be first and foremost made to publicly apologize to the young man. THEN, these kids should have community service in which they have to spend a period of time working with special education kids and learning about them. Then they need to be put into a position where they have to educate others on special kids and finally.....maybe the punishment should fit the crime. Maybe they need to have an "ice" bucket challenge of their own and have it filmed so that they too can have a taste of how this young man felt. Sometimes the simplest punishments are the best. These kids need to know that what they did was wrong and I do sincerely hope that whatever punishment comes their way....it is one they learn from and take that lesson through the rest of their lives.

Well there you have it....an update and my opinion! Boy you lucked out today!