Life never ceases to challenge me. Just when I get cocky, (ya know…because I have my toilets scrubbed and laundry caught up for 5 minutes)….a curve ball is thrown my way. I think God does this just to knock me down a peg or two and more importantly, to remind me that I’m really not in control of anything.
We found out this week that our youngest son, Avery, has Dyslexia. We have been concerned since he entered school, but all of our inquiries have been met by teachers with dismissal. ”Oh he is fine. He’s just young for his class and needs time to mature.” I didn’t buy it! I think there is much to be said about a mother’s intuition and having 3 other children before Avery who have navigated their way through Kindergarten and First grade, I had a pretty good sense of what his skill set should be at each level. While I understood that Avery was indeed young for his class (he has a May birthday), I still had a nagging feeling that more was wrong than just a little immaturity.
After all, he wasn’t misbehaving in class or struggling with his social skills. His math skills were right on point. But he wasn’t learning how to read no matter how much we worked with him. And his spelling was even worse than the reading. It was awful! I’m not being mean here, I’m just trying to point out a couple of the umpteen warning signs that were present, but never noticed by a single one of the many teachers that have been in his life over the years.
The only clue we got was when I was talking to a friend of mine, who happens to be a teacher and has a son who is also Dyslexic, about my concerns with Avery. It wasn’t until her son was in 6th grade and still couldn’t read that he was finally diagnosed properly. Because of the struggles that this poor woman and her son went through, she recognized many of the “symptoms” I was mentioning to her regarding Avery’s academic struggles. She gave me a name, phone number, and website to find out more information. I stumbled away from our conversation feeling dazed, confused, and perhaps a bit hopeful…hopeful that I’m not crazy and hopeful that if we can figure out what’s really going on with my son, then we can deal with it appropriately. I am a firm believer that nothing is left to chance. That casual conversation was not merely “luck of the draw”. God speaks to us through many mediums…quite often through other people. That day…that conversation….God spoke to me loud and clear through the words of a dear friend.
Moving forward, I did my research and set up an appointment to meet with the director of the local Dyslexia Reading Connection. It was clear from the first 30 minutes on the internet that Dyslexia was indeed what we were dealing with….the meeting was just a formality at this point. So, we met with the woman this week and found out after going through a lengthy assessment, that Dyslexia is pretty much all it could be. There is a $700 test we can do to have an “official” piece of paper proclaiming its Dyslexia for sure, but she said with the high cost and ruling out all other options, there is really no point to it. She mentioned that if the official documentation from the formal test would get us anywhere with his current school system, then it would be worth it. Unfortunately though, his school is in no way equip to accommodate his needs. The teachers are not trained properly on how to teach to a Dyslexic child. After all, they were not even equipped to notice the warning signs, so needless to say, my faith is rattled considerably in their ability!
Which brings us to the next hurdle….where do we go from here?
Our options:
We can keep him in the school he currently attends. I can then run him to tutoring 3 days a week, year round, for a minimum of 3 years after school where he would then have to come home and try to get homework done on top of the 9-hour day he has already put in. And the cost for the tutoring is astronomical! Insurance won’t cover it because they claim it’s a learning disability and the responsibility falls on the school system. The public school system claims it’s a medical condition so they disown any responsibility to help either. It’s madness, and the only ones suffering are the kids falling through the cracks and the parents struggling to pay for the help their children so desperately need.
Our other option is to pull him from his current school and enroll him in a local non-denominational Christian school that caters to working with Dyslexic children. Its a “normal” school, meaning that many children without any learning disabilities attend, but all of their teachers are trained in Dyslexia and are prepared and willing to meet the proper classroom accommodations Avery will need as he goes through elementary school and even into Middle school. It is only 15 minutes from our home and they even offer the tutoring he needs built right into his daily schedule. This means that my little 7-year-old will only need to put in a normal day’s worth of schoolwork without the extra time after school for additional tutoring. This option seems like a no-brainer; however, the cost for tuition alone at this new school is double what we are paying where he currently attends. And on top of the tuition, we still need to pay the tutoring cost, but they do offer that at a substantial discount from the normal fees, if he attends their school.
Either option lands our world in a tailspin. I will most definitely need to get a part time job on top of the full time, stay-at-home job I already manage. We have many decisions to make regarding his care and very little time to pull the trigger on either option.
So, overall…I feel lost! I feel scared and sad for my son because all parents want the very best life for their children with the least amount of struggles. While I realize fully that this is not a death sentence for Avery…it is a life sentence.
He will deal with this issue forever and that breaks my heart. School will never come easy for him. He will always need to work twice as hard as the kid sitting next to him in class does. It pains me to know how hard he will need to work at such a tender, young age when all he should be worrying about is playing with his race cars and running around with the neighborhood kids.
And I will do my best to see to it that his world remains as it should…full of carefree wonderment. But deep down I know that there is only so much my love can do for him…there is only so much I can protect him from. This is apparently his cross to bear….as it is now mine too, and I will be by his side to help ease his load whenever possible. And when I cannot, I will fall to my knees and pray that God will step in where I must let go.
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PS I will be posting links to as much reputable Dyslexia information I come across so if you have concerns or want to educate yourself with the warning signs, the resources will be available to you.