This is part of the 31 for 21 Blog Challenge!
Pre-Tessa, I had heard of Physical therapy, speech therapy, and even OT wasn’t completely lost on me. However, Developmental therapy (DT) is a totally new concept.
We get DT once a month, but now that Tessa is sitting, we will increase to once a week in November-ish. A developmental therapist is kind of like Tessa’s first teacher. She works with her on intellectual development – concepts like “in and out,” cause and effect, object permanence, all that fun stuff. During sessions, we play with toys and watch to see how Tessa interacts with her environment. In the beginning, we worked on getting her eyes to track objects and to show interest in faces, then toys. Our DT also works with our family to get us connected to the Down syndrome community. We talk about our own emotional development, our concerns and frustrations… I don’t know if this is in her job description, but Shannon has been a bit of a social worker along with Tessa’s DT. 🙂
Right now, our major hurdle has been Tessa’s startle response. When anyone (besides Ellie, that is) laughs loudly, Tessa displays the same kind of reaction that you might see in a child who was just given a shot. Sweet little pouty face, big fat tears…. She has the same reaction to dogs barking. Other loud noises don’t affect her at all. We sit right next to our Praise Team (essentially, a band) in church and she has no negative response to the music. When we play peek-a-boo with her, she often cries when we reveal our faces. Some strong smells bother her as well. I know that many people who interact with Tessa feel bad when she gets upset. However, it’s important for them to know that we would rather teach Tessa to react appropriately than to create an environment in which she doesn’t have to deal with this stuff.
Sometimes, children with Down syndrome can have a sensory processing disorder that causes them to struggle with different types of input. We don’t necessarily think this is something that Tessa is dealing with, but it’s certainly part of our conversation about her development. It’s something that we will continue to work on with her DT and also in occupational therapy.
Soon, Tessa will be at four therapies a week. Sometimes, that can feel like a lot. Right now, two therapies (Speech/OT) are at daycare and two (PT/DT) are at home. We just recently changed her Speech time so that I could potentially be there to help out with that. Recently, she hasn’t been able to get through a session of speech without crying uncontrollably or shutting down and going to sleep, so we hope that my presence will help her manage her feelings better. So far, it has worked. I don’t know if it is realistic to think that front-loading all of the therapy will help her in the long run or not, but if nothing else, the consistency in our weekly routine is nice. Plus, the therapists give some really great tips for working with Ellie, too. She is more work than her sister most days!!
Still cute when she cries.
Pumpkin. I just want to squoosh her. Peanut gets DT, too…about every other week. Funny enough, I’m not quite sure what it entails, but every time her DT leaves, it’s like she’s unlocked a li’l section in Peanut’s brain and she does something wonderful a few days later. Should blog about it. 😀
Isn’t that funny? The same phenomenon happens with us – it’s like Tessa is just waiting to be told what to do and she does it. Or, she hears us “threatening” more therapy work and decides to step it up to avoid working so much. 😉