May 6, 2015

Word up


I have had a lot of friends lately posting about their kids cute words and comments about things. I love to read them, kids really do say the darndest things! However, it makes me a little sad because Chance is nowhere near talking. I think if he swore or told me to shut up or something, I wouldn’t even be mad because I would be so excited that he said it haha I have blogged about Chance’s speech before. This post will be an update and some back info, incase anyone else is going through the same thing.

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Chance’s expressive language is about the level of a 8-12 month old (He is 21 months old). He has started babbling more and making a few different consonant sounds He says dad and dog but I don’t know if other people would know what he is saying. The word that I’m going to consider his real first word is “ball.” It’s more complex than “da” and could be identified by a stranger.

We sought help from Kids on the Move. I was very frustrated. They told me to do things that I have done his whole life (read to him, talk to him constantly, encourage speech, etc). They did all sorts of tests on him. They were not able to find anything wrong with him. This was a relief but frustrating. If there’s nothing wrong with him, why wont he talk? I honestly felt that since they couldn’t find anything wrong, they started to attack my parenting. We had been doing a few signs with him. They told us to increase our vocabulary and sign everything that we say/communicate to him. This was overwhelming for us. We tried to learn as many signs as we could. He was somewhat receptive but not as much as we would have liked (or kids on the move would have liked).

Upon further visits, they stressed signing everything to him. I didn’t feel good about this approach. I didn’t feel that it was right. Chance loves to sign, which isn’t a bad thing, but we need to encourage speech at this time. He started to refuse to learn new signs.

Grasping for straws, his speech pathologist decided that he lacked oral stimulation and suggested I get a device that he could chew on. It sounded like a baby toy/dog toy to me. And I didn’t feel that this was right for him. I had felt uncomfortable with her methods and lost sleep over it. After the last visit I cried for over an hour! How could I do so poorly as a parent? I have 2 degrees, if he really has all of these issues, how have I not noticed them before? I felt terrible. I expressed my concerns to Travis. He was done with it all and he canceled service.

Right now we are just working with him, basically continuing to do what we have done his whole life.  He shows no other signs of delay and is actually advanced in everything except speech. He continues to sign some words but has transitioned to some sort of word/sound for the things he used to sign. We have talked to many people who have had kids (seems to always be boys) that have had delayed speech that are intelligent and have no problems later in life. If Chance nears age 3 and hasn’t improved considerably, we will likely seek professional help through a private avenue but for now we are just celebrating his successes and encouraging him along the way.  It’s so easy to pick someone apart and focus on what needs work rather than what they are really great at! And Chance has MANY things that he is really great at! He makes me a proud Mama!

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People have the misconception that if someone can’t speak, they are unable to communicate. This is not the case at all with Chance. He sends and receives non verbal messages all day every day! This is actually quite advanced for a 21 month old. He can read emotions and acts accordingly. I rarely notice that he doesn’t talk because we communicate so well.

I realize that this is such a small and insignificant trial as a parent. However, I did not anticipate having a child with this random issue. It has taught me patience and made me realize that there is only so much you can do as a parent. It ultimately lies with the child. I think this is good for me to realize now, before Chance is even 2.

Sorry, this turned into quite a lengthy post but I want to document our experience and let other people know that they are not alone.