Showing posts with label autism in families. Show all posts
Showing posts with label autism in families. Show all posts

5/28/2015

Happy Birthday Grandson Ty!

As more and more children get diagnosed with autism, the field opens up to continued
hypothesizes of what causes it and the best ways to treat it. These include the practical to the outrageous.  I am astounded by the reactions of the public, in particular by those untouched by the diagnoses directly. And I must admit, frankly I was in that class as of 4 years ago. That was until the advent of my darling grandson Ty Ryan’s diagnosis in 2011.  Now, as he celebrates tomorrow his sixth birthday, May 29th, we honor not only his birth but his advances with his therapy.

Herein lies a boy whose parents were told he would never speak. And yet, one day I will never forget, his mother proudly called me to tell me she had placed him in his car seat. As she was driving down the road and dodging traffic, she clearly heard him say Mommy, not once but twice. 

This is a boy, who though autistic children are often times incredibly difficult if not impossible to potty train at a reasonable age, has been trained at an appropriate age.

Most autistic children will not make eye contact with strangers. Ty will most definitely do this and in addition to smiling says hello when prompted.

The list goes on and on of accomplishments of this astounding little boy.  I think it is due to parents that are steadfast in their devotion to pushing him the extra mile, getting him the best therapists and also getting great therapy. And I also believe he is gifted. 

The last but the single most important element in this soon to be six year old’s life is the presence of God.  He is surrounded, at all times by Christians, friends that believe in the power of prayer.  They believe in prayers for him, his family and for praying for continued progress on his journey.  His milestones show that the prayers and faith are working.  Also we all know that due diligence and positivity matter.

As a grandmother of one of these very special chosen children of God, please no longer ask me what is wrong with my grandson.  Refrain from asking me if my children did something to provoke this condition I  find this question offensive actually.  God makes things in life happen for a reason. I did nothing to provoke cancer and they did nothing to create the condition of autism. Let us celebrate his life! 

Do not look at my grandson with anything but joy.  Do not reflect on him sadly. He enjoys his life and so should you. Children pick up on others perceptions of them. It is wrong to label him anything but a child.

 If you see me, my children or anyone else struggling to control a smaller child, do not stare, nor be judgmental.  Kindly look away.   You are not always aware of the child’s condition, what the parameters are. 


I recall being at the Zoo Easter Hunt in line to enter the event and my grandson was upset. Everyone in the line was staring at him. This does nothing to aid the situation, not for him or any child for that matter.  What is the purpose of staring?  It simply embarrasses the child and he is receptive to feelings also. Please don’t embarrass autistic children; they have feelings just like everyone else. Give them their privacy when they are uncomfortable. 

I am in awe of the progress Ty has made and of all the hurdles he has climbed. It feels like he is continuing to defy the odds set before him.  Please continue to pray that better forms of therapy will arise and more research dollars are funded to continue the effort for this special population. May the next 6 years of young Ty’s life be even better than the first 6! 

Love,

Your proud beaming Grandma

Birthday Video for Ty Click here to View




10/03/2013

Autism Changes Like the Seasons


 Fall is somewhat like spring in the north.  Forget about sweatshirts down here; you can still wear flip flops outside. Heck, in the south folks wear them year round, right through the dead of winter.  And on Sunday, the end of September was one of our typical beautiful days that make me fall in love all over again with middle Tennessee.


Last year we spent a wonderful day at Lucky Ladds Farm with the grandkids and their parents in Eaglesville, TN just south of Nashville.  Just when I thought it couldn’t possibly get any better, this year it was just fantastic! One more year of intense therapy for my two autistic grandsons, Jake and Ty Ry and the changes are unbelievable. I am not sure, sometimes they are even recognized as being ‘special needs’, especially our youngest one Jake. 

I smiled with pride as I stood back and watched them both on the Farm.  I snapped away with the camera every chance I got.  My friends, the Lameys say I am like a foreign tourist with my picture taking! With these kids, I want to show the world what a happy family looks like with autism in their life.  My son’s family refuses to let a diagnosis stop them from living life to the fullest.  

As we entered the farm, surrounded by a sea of pumpkins and people, my two grandsons walked on their own this year, no longer shy or having reservations about going someplace new  There were no meltdowns, no heads bent, nothing of the kind. They were as excited as every other kid in line waiting to begin their wild Sunday adventure.  Jake was taking it all in, saying a few words and sentences, at the age of three, much like some of his peers.  Ty was giggling and laughing, just like the happy boy he usually always is; he adapts now so much easier to change.  

Lucky Ladd Farm is stock full of things to see and do. There are farm animals fenced in to feed, a petting area, slides, corn maze, rides and other things beyond this.  Ava, the big sis, in one year’s time has dramatically improved her language skills.  Now she is keeping pass with her kindergarten class that we weren’t so sure she would be in last year.  She easily expresses herself, in no uncertain terms, like every other five or six year old emotional little girl. 


Oh, we stand back and try hard not to laugh, as her parents find ways to lay down the law to their strong willed daughter without breaking her spirit.  But, as grandparents, we cave in. “You want a horsey ride? Here is $5.00, pick out a horse to ride honey, and go for it! ” What are grandparents for? 


Last year, Ty was completely afraid of the animals.  His mom reminded me of this the other night.    This year, our courageous little grandson was amazing, a changed little boy. He was fascinated by all of the animals and could not take his eyes off of them.  He was engaging, feeding them and allowing his


daddy to hold him close so he could get clear access to their mouths and feed them from his hands.  Grandpa and I stood watching, forgetting most of the time to snap pictures.  We were in total disbelief. Where was our little frightened grandson? 

Gone are the two little boys who hated being near others.   This day, thanks to their parents and the therapists’ hard work, these kids mixed and mingled with everyone.  Whatever they wanted to do, climb or see, no one was going to stand in their way.  Anything they saw they wanted to do, they went for it. No tears, no fits, no whining. Even the highest slide was not off limits to these boys.  Each boy went down first with their daddy, my son, gently assuring them they were completely safe and could do it alone.  Next time, he sent them down alone asking them to help him count to three, and down they went!  Not a peep from either of them except as soon as they hit the bottom of the hill, round they ran to climb back up the hill for more.

There was a huge shelter area that had corn kernels in it.  Supposedly autistic children are funny about things on their hands, or people in their space.  Ah, Jake was in that area, front and center, dumping the bulldozer, filling the dump trucks and as far as being around the perimeter of the huge area, no he was not having that.  Even with all the children in there, he was determined to be dead center, and that is where he remained the entire time until I had to drag him out.   And I do mean physically pick him up to remove him because yelling his name did no good. He would ignore us and then respond occasionally with a “No Grandma” because I was not mommy or daddy so he knew he could get away with it!   


It was time for Jake to move out of the pit, so to speak and see more of the farm.  Slide time was now and his mother had instructed me his melt down recovery time had lessened and that he was not to always have his way. I braced myself. His fits in the past have been long and pretty loud and inconsolable. Well, Jake told me no loudly and started whimpering.  I promptly said yes to him, and walked in the middle of the corn pit, swiped him up in my arms, and told him we were going to the slide with mommy and daddy.  Those little feet and legs began kicking.  As soon as I said stop it, they did!  Wow, therapy really does work!  Shocked I put him down and off we went to the slide, with a smiling little guy with no tears to show any discontentment. 


Ty, once notorious for meltdowns, is now the calm little boy his daddy once was years ago.  When he breaks down in frustration, from being overstimulated or overly tired, he calms down quickly for the most part.  I have been instructed what to do and found out Sunday, it works right on cue.  On the top of the slide, I could tell he was getting ready to have a meltdown. When I tried to settle him down, he seemed more agitated with me. I could sense what was coming so did exactly what my son and daughter-in-law have told me to do in the past. I picked him up snugly and when he began kicking, swinging his head, and continued yelling,  I simply confined him up against my body tightly and walked him out away from everyone in a nice quiet area.  I put him down and he was immediately fine!  He literally looked up at me and smiled!  We walked over towards the swings and all was well with the world.   No more long extended meltdown.  What a big boy; I could not be prouder!

Standing out on the acres of Lucky Land Farm that was covered in gorgeous landscaped flowers and haystacks with scarecrows, it looked like a children’s and adult’s playground.  Gone were the worries of the world.  Also, gone were the labels that the world puts on children.    Those silly labels mean nothing; they are judgmental statements that need not apply. 

Please take a few moments and watch the video.  I made one last year also with my blog of the same trip.   It was to show the normalcy that exists in a family that, on the outside looking in, many people think is so different.  I also get asked a great deal how my grandsons are doing. This is an easy to way to let folks catch a glimpse of two very special boys and the loving family that is just as important to us as they are my two grandsons. Without the other three, those two would never thrive. 

This family, Mike, Rebekah, Ava, Ty and Jake have gone through tremendous growth this year. Major progress has been made in therapy. Ty who use to use some sign language, as he was told he would never speak, is defying the doctors. He is speaking some words now.    Hopefully, the images on the video reflect some of the changes in the boys.  Autism in the family requires this, continued work and continued growth.  It is a slow steady progress, with steps backwards, at times,  but more steps forward when things are going right.    It is a constant ever changing journey.

One of things I have learned from my family is that I can never totally comprehend what it is like, on a daily basis, to have autistic children in the home. The best I can do is try, try to understand.  If we all do that, as a family, as friends, as a church community and as a society, it helps. 

Recognize too, my kids never complain. They love their children and would not change a thing about any of them.  We would not, as grandparents, want to change anything either, not one hair on these darling children’s heads.  Our grandchildren are as God planned, like all children are. 

Many children do not have parents who can care and give them the alternative therapies these kids need.  We simply ask that others have compassion and pay attention to the legislation and the changes that need to be made to help these children, their families and the adults with autism to assimilate progressively to the world.  They deserve it.  Having proper therapy to be the best they can be and reach their full potential is imperative as a larger population is going to become an even greater segment of our adult demographics of the future. 



These children and their families deserve to feel like they do when it is a beautiful day in the fall and they are at a pumpkin farm.   Just like the video below conveys. At the end of the day, that is what they are.
                  
                                       CLICK HERE TO VIEW VIDEO
                              

Sister Bonds

  Having spent some time recently with my older sister, it reminded me of so many shared moments in our youth.   Those years were some of th...