Silent No More: How an Early Intervention Program Changed Our Lives
After a routine checkup appointment with Max's pediatrician, she recommended we contact our state's early intervention program (sometimes referred to as Birth to Three) and have Max evaluated for any developmental issues that might lend cause to his lack of speech. It was her expert opinion he was just a slow talker, but the testing was free and could shed more light on Max's situation. We called, scheduled an in-home evaluation, and were off to the races.
Two women, a speech pathologist and a teacher, converged on our home and tested Max in a variety of developmental areas. The second half of our visit consisted of an interview with us, Max's parents, to get a better gauge of the case. In a little over two hours after they arrived, we had definitive results in our hot little hands: Max had a significant expressive speech delay, and minor delays in the areas of fine motor skills and self-help. It was recommended that a speech pathologist work with Max every two weeks for 6 months, at which point a reevaluation would be conducted.
If we had known about the statistic that 30% of twins and higher multiples have communication problems, and that boys are at 2/3 greater risk for delays, that might've saved some stress in the beginning of the whole process. Plus, being born four weeks early might've contributed, too. Regardless of the cause, we had the information and we were going to try our best to make a change.
Fast forward a few months, lots of in-home visits, and one speech pathologist who became a part of our family later, Max now tests well within range for expressive speech. All the singing, reading, stressing, reservations and researching was well worth the result: one extremely chatty boy. But, it doesn't end there. Had the outcome been different, his progress a bit slower, our local school system would've taken over after Max's third birthday and continued helping him in a preschool setting.
Bottom line: If you have concerns about possible delays, first check with your pediatrician. But, don't be afraid of discussing early intervention. The benefits could make all the difference.
It did for us.
About Sherry Pardy
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You bring up some important points about milestones. One of the biggest difficulties in being a new parent is the unknown. We are inundated with information as the proper progress of our children, and when they don't fall in line, which they rarely do, we freak out because we feel something is wrong with our child when in fact that is not the case. We suffer today from too much information
Thanks for sharing such a personal story. It's never easy, even when things are going well, there are always so many things to worry about as parents. It helps to talk to people, as you've pointed out. Nice work.
Our daughter was 18 months and still not walking without holding on to a finger. We got lots of helpful advice from friends and family like "oh, she was 5.5 weeks early, she'll catch up" and "she'll walk when she's ready" Lots of things that kept us from taking her to see someone. At her 18 month check up the DR recommended a physical Therapist evaluation. Two weeks later we were in her office.
They said Everything looked fine and our daughter was just being lazy (which is what we figured)so we decided to hold off on weekly therapy.The week after her evaluation she started standing up alone. The very next week she started walking.
Sometimes I think kids just need to know you're serious about the development stuff!! he he.
My son is 22 months and could barely talk. I got the same answers from my families. "Boys take longer..." Our pedia said wait until he is 24 months. But as a mom, I followed my gut. I contacted early intervention 2 weeks ago and they will meet with us next week. I'm pretty sure there is nothing to worry about, but an extra mile of research and a couple of professional intervention will do me no harm but peace of mind.
I will keep you posted...
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