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Re: I'm biting the bullet to put in the call tomorrow. (EI related)
And thank you! Your anecdote makes me very hopeful! My DH also said I should just wait to talk with the pedi first. This is me and classic impatience sending me into panic mode.
Justin + Laura 10.18.08
TTC #1 09.10/Dx PCOS 12.10/BFP #1 12.29.10/EDD 9.10.11/Missed m/c 2.3.11/D&C 2.15.11
“Ever has it been that love knows not its own depth until the hour of separation.”-Kahlil Gibran
Cycle #1 4.2.11 + Clomid = BFN/Cycle #2 5.9.11 + Clomid + Trigger Shot = TWINS!
Walter Allen and Eleanor Joan 1.15.12
Another baby on the way! 8.25.14
I really appreciate the kind words and encouraging anecdotes. Thanks for putting up with my anxious ass, guys. :-) I know I really need to learn to chill the fuck out sometimes.
Now that I've been talked off the ledge, I'm thinking I may just talk to the pedi again about it first and then call if he thinks thats the best option.
My son is 3.5 and if you look at all my back posts, I was in a similar spot like you a few years ago. One exception, my son walked at 13 months and had 5 words by 18 months. So, my son had more speech and was walking in same age time frame.---- but long story short--- still requires speech therapy at 3.5 and will for a very long time. He also has a combo of occupational therapy and physical therapy. He had gross motor movement that allowed him to walk and appear normal and fine motor movement that looked fine but it was not age appropriate. Example: he could play with toys, but still struggled at 3 to use a spoon correctly. His speech has slowly caught up but he suffers from a mixed receptive/expressive speech delay. Basically it means he doesn't understand speech at the level a kid would for his age.
I started out with a hearing test at 22 months (to rule out hearing problems as the cause), then he got evaluated by a private SLP and started speech, then got evaluated by EI to get a combo of services, then he got evaluated by a private OT that and started OT services with her. Then we got his vision checked after talking about how clumsy he was and we didn't realize how farsided he really was (+6 and thats really bad)
Please realize even if you start the process, wait times might be weeks if not months in order to be seen.
We have no one in our families with any sorts of delays. In fact, most of my and DH's families are college grads. I was caught between a gut feeling and people trying to convince me I was overreacting over little things. It is scary to seek out help. I totally get that. I was worried that they would tell me I was stupid as a FTM for thinking something was wrong, but I was also worried they would tell me he was autistic. (which right now he has red flags for but not currently DX) What looks like no big deal at 15 months can quickly turn into several other new things. For us, stuff kept cropping up that was odd. I am not trying to scare you, but please do not ignore it. Obviously something seems "off" or you would not have posted this.
Give your son the best chance and yourself piece of mind and get the ball rolling. The worst that could happen is that you spent a bunch of time getting him evaluated only to find out he was fine. I could literally write a book about all my experiences with my son. I will spare everyone the novel unless you have any specific questions for me
What's the hardest is that no one can tell us the outcome for him. I have him involved in as many therapies as I can and early intervention is really the best. If you ever have any questions in the future, the Special Needs board is a great bunch of ladies. Hopefully I won't see you there, but if I do, they are a great network of support. Its nice to know you are not alone!
My DD didn't have any words at her 18 month appt. I was concerned and wanted an EI eval. Her pedi disagreed and said that DD was a great communicator non-verbally and to give it one more month. At 19 months, she went through a crazy explosion and was talking in simple sentences by 21 months. She is now 2.5 and is super verbiose. A lot of kids are late bloomers.
That being said, anecdotes are anecdotes. I always think it is a good idea to get an evaluation for a few reasons. 1) They can put your mind at ease. 2) Even if a child does not qualify, the evaluators often give parents advice and strategies to help improve their child's skills. 3) If you child does qualify, starting professional intervention early makes such a huge difference.
I say this having gone through an EI eval for DD for her gross motor when she was an infant due to Torticollis. It can be scary, but at least you get an answer.
Good luck.
He how for his 15mo appt this friday, so I'll definitely be talking to the pedi and I'm sure he'll recommend an eval at this point.
Trying my best to be patient....but gah! Patience is hard!!