Thursday, November 8, 2018
No Words
Sunday, September 16, 2018
When I Knew
NOTHING and EVERYTHING all at once, the perfect PARADOX
Today there is:
Juancho
Do you really need to hold 6 different stuffed animals at once and cry if one of the fall to the ground?
Why are you running back and forth on your tippy toes?
Are the sounds really hurting your ears?
No coincidences, just blessings in disguise. Just at that time. At that exact time. Time stood still for what seemed to be about three years and at the same time, Time: it just flew on by and all of these thoughts circulated for what felt like three seconds.
It is all making sense but I still don't get it.
What do you mean my son has autism? Wait, OK that is why I am here. I am here to tell you my son has autism. What IS Autism? What is our next step?
Whatever it takes.
WHATEVER it Takes.
WHEREVER it takes u.
I will make sure you fit in, all while standing out.
You will stand out. You were born to stand out.
After that day, I hugged him a little tighter and loved him more than ever.
Sunday, September 2, 2018
A Super Power
He is not lucky; he is blessed. Blessed that he can speak, blessed that he can hear, blessed that he can walk, blessed that he can eat and live a healthy and happy daily life of a child.
Autism does not inhibit him. Rather it inspires him and pushes him beyond limits that society has placed before him.
He did not speak until the age of three and half. He was at doctor appointment after doctor appointment. He saw many specialists. He also went to speech therapy and occupational therapy outside of school. He started Pre Kindergarten, in pull ups and not yet able to verbally communicate. He was placed on the middle of the spectrum and was given a label.
I am thrilled to say that he is high functioning and thriving! With LOVE and dedication, with hard work and determination and with acceptance, his world is one of joy without limits.
I often forget that he has an autism diagnosis. He is like every other typical child yet at the same time, so very unique.
If a parent does not want to admit or accept that their child has autism and does not seek out help, they are doing a disservice to the health and well being of their child. There is nothing to be ashamed of.
To learn of JJ's journey please refer to the archives where I have his stories posted.
Any questions or comments, please feel free to contact me.
There is still so much to share.
xoxo
Dany
Thursday, June 4, 2015
Yes, He Can
He is healthy. He can see. He can hear. He can walk and he can talk.
No, you won’t!!! Do not worry, you won’t catch it. Do not back away. Do not put your guard up.Autism is not a disease. It is not even a disability in my eyes, on my end of the spectrum. I can only tell you my from my point of view but I can speak for all autism mommies when I say that autism is not a disability, but rather, a different ability.
He needs room, he needs space. He gets easily overwhelmed. His senses can get overloaded. The lights, sounds, textures sometimes can be a bit much. But he is capable, he can do it, sometimes it will take a little more time and patience but I will never give up on him.
Yes, autism is a different ability. My son is not disabled. He can walk, see, eat, play and do many other things. I know I am not missing anything but that does not constitute as being disabled. He learns in a unique way but he does have that super capability to learn and therefore will be a different abled boy because the world is obsessed with titles. That is my title for him.
He listens at the same time he is in his own world. I wonder what it is like, what goes on his mind. It must be so vivid and colorful, at times to much to handle and process.
Like many others on the spectrum, my son has super abilities. Ability to grow, to shine and to even lead the way. Stop staring at him, you will not cure him. You do not have to be afraid. He may be flapping like that because he is super excited. How great is that? To be a child and to be overcome by joy over something that may seem miniscule to you. That is an outlet, an escape when one is overly stimulated. That may be the body’s way of responding to the outside world. Why would I want your cure anyway and why would a proud mommy want to cure a child who is beyond special. A child who knows how to love. It does not matter what doctors say. No, repeat after me, it does not matter what doctors say. Have faith in your child. That, that unwavering faith and determination will help your child in so many ways. It does not matter what the onlookers say, I know my son and he will be somebody someday. No, wait, let me say that he is somebody today and he matters, his life matters.
Our autism is a blessing in disguise. He is not a brat, he gets over stimulated and hyper focused. He is very sensitive and if you dare to enter a minute in his world, would you be able to handle it? Handle the stares? Handle the talk? He got this, we got this and God got us. That is what matters. He matters and autism does not, it is just a word to call something that people do not yet understand. Cause ya know, everything needs a label, right? So, don’t worry you won’t catch autism but if it were at all possible, you would see a world of infinite possibilities. And, that is not so bad after all, is it?
Autism is not just stim, stim, flap, flap..oh no, it is so much more than that. The joys it brings the doors it opens. Yes, I am happy that my son has autism. I am happy that on paper, at school, it states my son has autism. That is because he gets the one on one attention that he needs and deserves. His needs are being met through an IEP. That is what he needs, an educational plan that is individual to and for him as it should be. Many of his autism symptoms subsided. I have not seen flaps, stim- phew in a while but it may happen and I do not mind at all. He has one last appointment with his neurologist and then he will be dismissed due to not showing signs of being on the spectrum. This is great news, but I want my son to be autistic forever, especially on paper, in school where his special needs are met through specific educational goals just for him.
Yes, I am happy that my son has autism. He has paras, therapists, teachers, social worker, all for him. All for growing his educational experience and making it valuable. For that, I am grateful. The label is there but for the better good. It gives him the opportunity to have his education catered. To have opportunities that other children do not have, although may need. I like that he gets extra positive attention from school personnel. It is what he deserves as well as all children. It is too bad that classrooms these days are stuffed to the door, with over 25 kids and one teacher. Kids’ needs not being met, simply no time for everyone. Then, they fall behind. They lose desire and feel neglected. That is why I am grateful my son has autism..he gets what is meant to happen for all children, but he gets it and I guess you could say that is pretty special. He has special needs but all children are pretty special if you ask me. He is just lucky enough to have autism. It can be intense. It can be overwhelming at times – but most, if not all things that are worth it, are. So, yes, I am a proud autism mommy and no I would not change it for the world.
Please, keep picking my son up right at our door each school morning. No, I do not care that it is a small bus. They cater to my son, door to door service. Blessed he does not have to walk or wait at a cold bus stop or that we do not have to drive him all the way to school, on the other side of town – He has a bus attendant and also people that wait for him at school to help him off the bus. So now tell me how my son has a disability. It really is a super ability if you ask me. He has OT and ST services. So, please do not feel sorry for my son but rather let me as not only a mommy but a differentiated educator, tell you that I feel sorry for the kids who do not get the attention they so need in school, then fall behind and end up disliking school. I am beyond blessed that my son loves school. Beyond blessed that he has autism. So what, you won’t catch it. I am sure he could teach you a thing or three. So, what is this PDD-NOS you speak of? Maybe, if you really think about it, it is not specified anywhere else because it is not a pervasive developmental disorder. I do not care that my son did not speak until he was almost 4 years old. The important thing is that he does speak and he can and for that we are blessed. So what if he grasped things and hit milestones later that what the world expects him to. What matters is that he CAN and he WILL.
Wednesday, April 23, 2014
The Case of the Missing Tooth...
Jorge Juan lost his first tooth!!! Exciting time, yes it has been. The tooth was MIA for a day but we got it back in a ziploc bag! Awesome, we were waiting for it. For several weeks, Jorge's front bottom tooth has been wiggly. Every single day I would have to check his wiggly tooth (only after measuring his muscles and height, and yes this was an everyday thing). So, the tooth was super wiggly but I thought it would be at least another week or so before it popped out. So, the tooth came out two days ago at school. He came speeding off the bus exclaiming that his tooth came out. Wow, it was awesome to see him excited. He said the tooth was in his folder, but we could not find it anywhere. My husband even called his teacher. Mr. G said he would look for it on the playground but he told me Ms. P had the tooth. Anyway, Jorge told us he lost the tooth because he bit into his apple then he pulled it out and the other version was that he was on the playground and bumped something and his tooth fell out. Jorge gave the tooth to the aide...OK, so he came home that day with no tooth, kind of upset because he thought it was in his folder and he wanted to put it under the pillow so the tooth fairy could come and give hi some money. At first, he only wanted coins but that quickly changed. Anyway, Jorge came home with his missing tooth inside of a ziploc bag yesterday, it was in his folder. His teacher wrote a note saying that somehow it made its way out but anyhow yay!!! the tooth is here.
So we talk about the tooth fairy. He was excited and we even made up a song to sing so the tooth fairy would arrive while he was sleeping. We put the tooth under the pillow. We left it in the bag and taped the bag to his mattress so there would be no chance of him losing it another time, lol. So he said he wanted paper money. He quickly and eagerly went to bed and slept on his pillow. The Tooth Fairy snuck in his room, grabbed his tooth and put a 20 dollar bill in the bag. The Tooth Fairy was going to give him 10 but I guess there was no time to go to the bank. Phew, we made it. I believe we were just as excited as him about this. So..Jorge Juan wakes up at 6;30 n the morning calling me. So my husband and I jump out of bed, we knew what it was. He was so happy telling us that the tooth fairy had left him a dollar. Yes, he still thinks it is a dollar only because it is a single bill. It is too cute. So, while waiting for the bus, Jorge Juan told me that the Tooth Fairy looked like Cinderella with wings. Ahh..just as I imagined. And she even talked to him as he noted she told him he was being good and listening so he gets one cent. Too funny. So, the case of the missing tooth has been solved. And now it is n safe keeping.
Now, if I did not tell you, would you know my son has autism?
Children are innocent. Their innocence is priceless, magical. It needs no other labels. A "typical" experience for a "non typical" child. I love my indigo!! To be a child..To find happiness in every little thing. It is pure magic. They have so much to teach us. My best professor yet and I always get an "A" .





