October 16th, 2005
Unifying Genre: Email Exchange
To: soccermom05@email.com
From: judybrooks1977@email.com
Subject: son with verbal apraxia
Samantha,
Hello, my name is Judith Brooks. This week my son Matthew was diagnosed with verbal apraxia. My friend Carol told me that your son was also diagnosed with this and he just recently finished his last therapy session. I've been reading about verbal apraxia and I know that it's also called Developmental Apraxia of Speech and that it makes it difficult for a person to speak and in Matthew's case, the longer his sentence is, the worse he sounds.
But I really don't know what to expect to happen when Matthew starts
going to therapy. So I was hoping you could tell me some of the
things that your son went through while in therapy.
With much appreciation,
Judith.
From: soccermom05@email.com
To: judybrooks1977@email.com
Subject: re: son with verbal apraxia
Judith,
I'd love to tell you about what our experiences are in dealing with verbal apraxia. Sammy (that's my son's name) required therapy 5 times a week and each session took 30 minutes. This lasted for about 8 months and then we only had to take him twice a week and each session was 45 minutes long. Sammy was in preschool when he started it and he absolutely hated the intense therapy. But as time went on, he began to tolerate it and would sometimes even be excited after particularly a successful session.
After about 5 months everybody who knew him could tell he was improving. My husband and I both wanted him to be able to say his name and he did just that after 13 months of therapy. He went from saying "Na-Naa" to "Shammy". He can now clearly say "Sammy" with no hesitation.
It's hard to be patient when it's your child that is suffering but just hang in there and eventually you'll see improvements. I found something that helped us was to keep a box or folder of everything we learned and did while in therapy. It was a great way to keep all the information together and it really helped Sammy to see how far he had come.
Keep me updated on how Matthew is doing and please let me know if there's anything I can do to help.
Sincerely,
Samantha
To: soccermom05@email.com
From: judybrooks1977@email.com
Subject: update on matthew
Hi Samantha,
I just wanted to let you know how Matthew is doing so far. He did his fourth therapy session today. He isn't the most thrilled kid in the world to be going to therapy every week but he does like his therapist. I get to watch him from behind a mirror and you were definitely right about it being rough to watch him struggle. He won't do too bad as long as he only has to say one or maybe two words but anything after that, the poor guy falls apart. I always feel like running in and hugging him but I force myself to sit and just watch the therapist help. She's really been a lot of help so far. That's not to say that Matthew's made any major accomplishments but at least now we know how to work with him at home in between therapy sessions. You probably had to do most of these things when Sammy was in it but now we do a lot of songs and practice on sentences that we use a lot.
I also wanted to tell you that I took your advice on saving everything he did and what we've learned. I suggested the project to Matthew and he was all for it.
The first thing we did was to keep all the information they had given at the clinic, such as a pamphlet on DAS and iformation from a PowerPoint Presentation (to be added) Matthew and I went to.
I spoke to a student named Chris Stout who's going to Marshall University to become a Speech-Language Pathologist and he told me that he has a weblog with a few links to information about DAS. Chris happened to be observing Matthew when I met him and he was kind enough to let me see what he was writing about on a form.
Matthew has also been writing about how therapy is going in a journal and he wrote a poem using the letters from "APRAXIA." I couldn't help but cry when I read it the first time. It just breaks my heart that my little boy is going through so much pain and I can't just step in a make it all go away. I didn't let him see me cry because I was afraid I'd upset him or think I didn't like it. He's really proud of that poem and he loves the idea of doing this little project. As soon as we get home from therapy, even before he eats, he writes in his journal and puts his speech homework for the day in a folder.
Anyway, I just wanted to let you know how it's going so far and to thank you again for helping us out. I promise to keep you updated on his progress.
I'll talk to you soon.
Judy