Speech Delays


We’ve been working with a speech therapist. It is a slow haul. I wish I could speed things up. She has been coming every other week but each week we have to start all over each time because Roo is so shy. The first 30 minutes is spent warming up and then we can get started but then it’s time to finish up. I got frustrated last week and asked her to come once a week in the beginning to help build a better rapport with Roo. She is open to it and needs to get approval. I’m hoping that it will get approved and helps.

Roo still has only a handful of spoken words at 23 months.

Mama
Dada
Blue – boo
Woof
Baa
Moo
Pa – for my dad but sounds like ba
Ma – for my mom
Yeah – for yes
No!!! – she’s got that down pat 🙂
Vroom
Wee – for cars/wheels
Wawa – for water
Ball – sounds like baa

She has more signs:
DownKangaroo
Cracker
Rabbit
Thank you
Please
Music
Different
Again
All Done
More
Food/Hungry – she uses the interchangeably
Wet
Car
Horn
Help
Fish
Bird
Duck
Milk
Hi/bye

She also has really good receptive cognition too, which is a relief.

We were recommended two books, which I really like:

The Big Book of Exclamations, which helps engage kiddos through storytelling

It Takes Two to Talk, which helps me as the parent to learn to slow down in my own speech to encourage her speech development – great for parents and caregivers (but is pricey – I borrowed it from the library before investing in it)

I’m hoping that she will start to speak more clearly soon! She’s definitely interested in “talking” more with babbling.

What books are you reading with your kiddos with speech delays or on your own to help them?

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Worry. Not Worry. Worry. Not Worry.


Being the parent of a preemie has a different set of rules. Rules that seem to change on a monthly, weekly, daily basis. It causes me to worry than not worry than worry and so forth. You get the picture.

Roo had PT/OT on Thursday. We hadn’t seen her therapist for a few weeks because of Thanksgiving, travel, and a presentation she was giving. I was so excited because during the time we hadn’t had therapy, Roo was making so much progress. She was vertical, on her feet as much as possible and letting us support her to walk around.

Her therapist was also excited but because of those new developments was able to see something that she either didn’t notice before or missed. We knew that Roo has low muscle tone in her core and that was causing the delays in sitting, crawling, etc. But her low muscle tone issues are now being noticed in her legs and feet. And, could be affecting her mouth, which could be why she is delayed with speech.

Next week, we will do her 18 month assessment to see where she is developmentally. I have mommy brain and can’t remember for the life of me what it’s called – maybe one of the other preemie mommies can jump in. She has always tested incredibly high in the 85th percentile for her fine motor skills and in the 5th percentile for gross motor skills. After the assessment is done, the results are shared with us and Roo’s pediatrician, whom we see on January 7.

I know that we will be referred to a speech therapist. I won’t be surprised with that referral. But, I think people are going to start pushing us to see a neuro specialist to look further into her muscle tone and delays. I’m hopeful that this won’t happen but it is something that my parents (doctor dad) is pushing for and I’ve been very hesitant to pursue – for many reasons. First, I’m scared. Second, I hate subjecting my daughter to test after test after test. I feel like every other month she goes to a new specialist for something or other. In October it was the allergist. Third, I’m exhausted emotionally.

Do I want to be sure everything is OK with Roo? Of course, I do. If there is something wrong with her, I want to and currently do everything possible to intervene and help her. I’m just not sure if I can handle if there is something more wrong with my little girl. She’s been through so much and I don’t want to have to put her through more.

A big part of me thinks she will catch up – like she has in the past. She is on her own timeline. She meets all of her milestones – just in her own time. Do I push for more testing or wait and see? I know that early intervention is best but why intervene when she will catch up eventually?

The last three or four weeks, she’s done so well that I want to keep riding on this “normal” wave. Yes, she doesn’t walk or talk like all of her 18 month friends do but she communicates beautifully with us and crawls with such enthusiasm that she sounds like a rhino running through our house.

I just wish that I didn’t have to worry about my daughter’s development (or lack of) anymore. I want to be a normal mommy who worries about what mommies of children who don’t have developmental delays worry about like should I be looking into preschool? Yes, the moms in my mom group are starting to look into preschools because of waiting lists, etc. I haven’t even thought about it and will probably wait until she’s three because she’s so tiny, which is not until Fall 2015.

Moms of preemies, please help me. What do I do? Do I push for more testing and early interventions or wait it out? I’m so confused and scared. I don’t know if I can handle another diagnosis that requires more therapy and doctor’s visits. How do you get through it?