MJ’s IEP meeting is coming up in a few weeks. Now that he’s 15, the IEP meetings are different and he can now be included during the actual meeting. Nothing much has changed in terms of his current teacher.
She still does not communicate.
She still sends home homework that she￼ neither looks at or grades.
She still sends homework that is completely inappropriate for his comprehension level and oftentimes has no clear instructions😡.
She is one of three teachers at his high school that teach the special needs kids that are in a self-contained classroom. I tried getting him switched to another room at the beginning of the school year and was told, “we tried, but that room is the best placement for him because he is considered higher functioning etc.” Still, Mj is happy and enjoys going to school. He has many friends in that classroom and most of them travel with him to the same aftercare. I really don’t want to take him away from his friends and familiarity of his school and environment. ￼￼￼￼ I am both dreading and looking forward to this meeting. All of these issues must be readdressed and resolved￼￼.
MJ deserves better than what he is currently receiving academically. ￼￼
I will post an update after his meeting.
Thanks for reading.
Well, our summer has officially come to an end. The kids started school today. MJ is now in the 10th grade and Morgan is now a seventh grader! Today’s morning drop off was great. Both kids were super excited and I know for a fact that my daughter didn’t sleep too well! When I got to the front of the school to drop off Mj, I was relieved to see his friends, all of the aides, and the ESE specialist waiting to greet all of the students! Though I’m not totally happy with Mjs current teacher, I am being optimistic about this school year. Here we go!
On the left my son is almost 15 years old. However, I still see him as the little boy on the right🤷🏽♀️. Yes, it’s unrealistic, but there’s something about my Scoompy that makes me want and need to protect him forever. I’m so grateful to God for every milestone he has reached and every obstacle he has overcome. We were once told that he would never speak clearly and didn’t know if his writing would ever be legible. MJ continues to learn and grow. And through the process, I continue to do the same.
I recently received this alert saying that I have been blogging for 3 years! I honestly cannot believe that it’s already been that long. I remember how nervous I was to begin blogging. Where MJ is concerned, I tend to be a little bit more private than I normally would be. MJ was ending his 5th grade year and hadn’t even started middle school yet! Boy was I anxious!!! As the days and months go by I continue to write and read other blogs and learn so much from other special needs parents. The knowledge and support that I have received has been truly wonderful. I’m looking forward to many more years of blogging 😁.
My daughter’s birthday is coming up. This year she wanted to do something different so I mentioned Disney and of course she was totally excited about it! I immediately went online to try and find what weekend would have less crowds. My daughter’s birthday is Presidents Day weekend and I knew that would be a nightmare for MJ ( heck, for all of us)! After researching I found that February 8th-11th is a non peak weekend and therefore would work well for us. When we do visit Orlando, we only focus on one theme park. There is no park hopping over here. MJ would never be able to tolerate that. My daughter decided on Animal Kingdom this time. I was pleased because MJ loves animals and I knew he’d enjoy it too. We always pack the essentials: gold fish, Caprisun, apples, headphones, portable DVD player and his tablet. Im so relieved that he does well on road trips. He is relaxed and mostly looks out of the window while occasionally asking, “are we there yet?” When we first get to the hotel we settle in and then walk around and check out the resort. Then it’s time to eat! They always have his favorite (nuggets and fries). Next up is always the arcade. It’s so nice to see the kids playing together and not getting on each other’s nerves (yes Jesus)! The next day is our theme park day. I prepared MJ by showing him videos of Animal Kingdom with the attractions and rides. We also reviewed a map of the park and the hotel we’d be staying in. When we first got there we immediately went to guest services for their “disability access service” which allows MJ to go on attractions a little faster, in order to avoid meltdowns. After that it was time to explore the park! MJ was a bit hesitant when we got there. He walked slowly, with his head down, and looked aggravated. Hubby had to hang back with him for a few minutes while I went ahead with Morgan. She was thrilled with all there was to see and I could tell that it bothered her that MJ was less enthused (insert prayer here). It took about 30 minutes for him to ” warm up.” We had fun on Kilimanjaro’s Safari, and on rides in the Dinosaur area. The Festival of the Lion King show was great! Unfortunately MJ slept through the entire show which was really a bummer because I knew he’d enjoy that (One of his favorite TV shows right now is The Lion Guard). Six hours flew by and I could tell by the look on his face that it was time to go. We are always sure not to over do it with him. After Animal Kingdom we had dinner then the kids enjoyed the resort pool for the rest of the evening and the next day. We had a wonderful time and though this trip was really all about Morgan, we can never really go anywhere without planning for MJ.
The only picture of All of us together that we took:
Ain’t this the truth!
Courtesy of @bloomingwithautism
Am I the only autism parent that believes some behaviors are not directly related to autism?
Am I the only autism parent that actually believes that early intervention is key-That we have to begin teaching our kids early on?
Am I the only one who believes that our kids can learn to say please, thank you, and excuse me etc?
Am I the only one that believes we need to teach/discipline our kids when we know that they are purposefully being defiant or disrespectful?
Am I the only one that expects her 11 year old child to know now that it is inappropriate to throw things across the room.
Am I the only one who has to teach her child not to yell at adults when he doesn’t get his way?
Am I the only one that didn’t take her child to church/ restaurants because there was no way he would be able to sit through a church service or meal; and refused to take him until he was ready?
Sometimes it is difficult to know if the behavior is related to autism or if the child is just being defiant. In my opinion, it is up to the parent to know their child and to know the difference.