Showing posts with label public school system. Show all posts
Showing posts with label public school system. Show all posts

Monday, December 1, 2014

Another One That's A Bit Overdue

Another One That's A Bit Overdue



 I know,I know, I have been slacking yet again. Life just gets so busy you know?! Colton started school in early September. I'm sure I had more stress and anxiety about it than he did. It has actually really been a great benefit to him. I've seen massive growth in his vocabulary and attitude towards other children particularly ones his age. In mid October he started extended days which has been tough because it wears him out and I feel as if I have even less time with him. I did quit my job at the end of October so I have actually had weekends with him which has been really great. He's starting to become really interested in letters and numbers and is just so very bright. It has been so exciting to watch him learn and light up when he gets things right. Our biggest issue lately has been potty training. 


Potty Training 


This has proven to be probably one of our biggest challenges yet. Colton is very interested in the concept of using the potty. He knows the routine and is open to books and movies about it. However when it comes to actually just sitting on the potty he flat our refuses and if the issue is pushed he has a meltdown. I can't figure out why he is so against it. He doesn't seem to be afraid of the potty and the idea of underwear is very appealing to him but he knows he must successfully use the potty to get those. If only they made Star Wars or Angry Birds themed potty books. I could see those helping. Perhaps it's time for me to get crafty! Now on to some positive things. 

Holidays 


For as long as Colton has lived he has been freaked out by holidays. This is the first year he has been excited for them and we have truly been enjoying it. He loves Halloween and everything that comes with it. We were able to take him to a carnival! He still wouldn't wear a costume but he was okay with seeing others in them. He is obsessed with Santa and he was actually able to sit on his lap and tell him what he wanted for Christmas (Chewbacca toy!). I can't wait for Christmas celebrations with him this year. 

Making A Friend 

 Colton has managed to make a friend of sorts. There's a little boy at his school who is similar in a lot of ways to him and they actually "play" together. By play I mean games like chase and hide and seek but this is a huge step forward for him. He likes to share with him (another big step). I am so happy to see this and very proud of him. 

In Closing 

Colton is making a lot of progress. So much so that I have people telling me all the time "Oh he can't be autistic" or "See, he's normal". Well that is the goal of loads of therapy isn't it?! I want the world to not see my son as a label but I do want them to realize that he is different but that it's ok. They don't always see what I deal with, the meltdowns,the extreme rigidity, the major prompting and planning that we do everyday to get through what we need to do. For example I always tell Colton the "rules" before we do anything. Such as we are going to a place to eat and here's the rules: we sit in our seat,we use quiet voices and we listen to Mama and Daddy. He repeats these several times to himself before and during and while it doesn't always work he needs that repetition to make it through. People never know what you go through with your life period. Don't make judgments about what others tell you. We are only trying to be open and fair to our son. We didn't ask for the autism but we accept it and we work with it and in some ways we enjoy it. I wouldn't have Colton be anything but himself. 




 Maybe next year he will smile for his Santa picture but hey at least we got one!


Wednesday, August 27, 2014

Way Overdue

It's really been far too long without an update. I could ramble off excuses:I had surgery,started working more often,vacation etc etc. However I just really haven't pushed myself to sit down and type. Anyways on with the updates. 

In June the day before Coltons 3rd birthday he had his last sessions with Birth To Three. It was a sad but happy moment. Colton has come so far in the last year. It's hard to believe that a year ago I had a child who did not talk and had extreme sensory issues. He still definitely has a lot to get through but Birth To Three was a godsend. I will forever be grateful for getting him into Early Intervention Services. I know those who go without these services can have a much harder time making up for them. Let me backtack a bit.  

In May Colton was tested to see if he would be going to developmental preschool. He was accepted into the program and will be starting school September 10th. I have a lot of anxiety about this. How can I be able to put my 3 year old on a school bus by himself and send him off to school? How will he deal with another person changing his diapers? How will he feel when he realizes he is alone? I'm sure I am overly worried about this but it's tough. Most parents get to have their kids at home until 5. I feel like I am having to go through this way too early. As with everything I know our family will persevere. It's just going to be a really hard adjustment. I worry that Colton will struggle with some reverting type behaviors.I worry that they won't understand him when he tries to talk,I worry he may not talk at school at all. All I can do is hope. I've been riding on hope this entire journey and I don't suppose that will change,ever. Now to talk about something great! 

In July we took a family road trip to California. This was huge,we never could have done this before. Yes, it wasn't perfect but it was better than I ever could have hoped. Colton made it through amusement parks full of people,noisy environments. He slept in a bed that wasn't his. He had his entire routine thrown off and made it through it like a champion. My son is truly my hero. 

I truly hope that I can get back on this. I feel awful for not "blogging" more considering this has been almost like a form of therapy for me. I also think it's important to tell Coltons story, and to share updates with friends and family. As always thank you so much for reading and for your support! 








Monday, February 10, 2014

Ups And Downs

Roller Coaster Ride 

 

 The Downs

I may as well start with the negative so as always I can end on a better note. I guess I will start with the school tours. 

Public School 

So we went about a week ago to visit the public school Colton would be going to in the fall.Keep in mind I really went in there with an open mind however what I found was difficult to process. First off the classroom is in a portable. It isn't even a real classroom. Then let's look at teacher-child ratio. There are two aides for twelve kids. It's okay but certainly not ideal. While it seemed that it wasn't a horrid place I will be honest. What I saw was chairs with restraints and what appeared to be a school dedicated to keeping these kids in special education not helping the ones who have potential get eventually integrated.Of course I am being a little biased, I truly have no real experience with the public school system and their developmental delay preschools but I just left there feeling sick. I dislike how the public school system defines my child as low functioning when I know he is very high functioning, almost a savant in some ways.  I also don't appreciate that he would be only 3 years old and in school five days a week for six hours a day.

ABA School 

One week prior to our public school visit we went to tour an ABA school. Not only is this a school where Colton would receive all of his behavioral therapy but they are guiding children to be able to get into regular 1st grade. They divide them up by ability not how they fall on a "normal" scale. In short they would be teaching my son to read, not strapping him to a chair. Also the teacher-student ratio is three teacher/aides to one child. That in itself is amazing. Here comes the negative news, our insurance of course does not cover behavioral therapies including ABA,not only that the school doesn't even work with our insurance company brand. Oh and did I mention it's $1,600 a month if you are self pay like we would be?! Yeah well we are pretty much back at square one. 

Upcoming Surgery 

I found out recently that a surgery I've been putting off can no longer be put off. It could be as easy as just three incisions and two weeks of healing or it could turn into a much more major surgery with a recovery time of ten weeks or so. This of course means it will be very difficult to deal with my toddler especially because he is so attached to me and doesn't comprehend other peoples feelings or pain (essentially like many with ASD he lacks sympathy). Thankfully my husband will be able to take some time off but I'm just having a hard time picturing how this will work out for my son or I. Albeit without this surgery things could be so much worse for everyone so I'm just going to go in with positive thinking, it's all I can do. 

 The Ups 

 Colton continues to be bursting with new words. He is responding so well to therapy at this point my expectations and hopes increase each day. I am so proud of how far he has come and how hard he works. He is really into spelling lately. If he sees a word he spells it out, I could listen to him do that all day! He has started to become more confident in himself as well. I believe that he is meant for some truly great things. He has started to create real bonds, maybe it's only with adults but it's definitely a start. Raising children is hard work, raising one with special needs is indeed a journey but I wouldn't trade it for anything! What's normal anyways? :) 

In Closing 

 Again thank you as always for reading and for your continued support. Autism awareness has come a long way but we still have a long road ahead but I truly believe that someday things will be so much better, more informative, easier. I also truly believe the key to this is education. Every time I encounter a "non believer" or a "skeptic" I do get upset but I also choose to take it as a chance to educate. Let us not forget that some people are just ignorant, what they don't know they fear, they don't understand. We as parents of special needs children are warriors, so are our children. Together we will fight their fight, even if it seems like an endless battle it is worth it! It will always be worth it.