So some of you might remember that our pedi suggested going to a development pediatrician and looking into early intervention for DS. He was not making some milestones at his 15 month wbv and was showing deficits in some areas.
We went this morning and the dev. pedi agreed (( More or less diagnosed him with Pervasive Developmental Disorder, which from what I understand is on the Autism spectrum.
He recommended early intervention - which we already had an eval. set up for anyways - and a lot of it...probably 10-12 hrs a week. So they'll hopefully go to daycare and home to work with him. His main areas of concern were communication, play and social reciprocity - 3 biggies.
Tough news to hear, but DH and I were sort of prepared. From everything we know, the most support the earlier you get it is wonderful and the doc this morning said that he was very hopeful that with a lot of support, DS could make a lot of improvement and hopefully by age 3 or so will be making awesome progress and the autism will "disappear" for lack of a better word.
Just wanted to let you know - your support means a lot!
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Re: update about DS - (autism related)
Ginny DX 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia
Charlie DX Specific Antibody Deficiency & ASD
Sorry the news you got wasn't all positive but so happy to hear there is a plan in place to get your LO where he needs to be.
It sounds like you and H are handling this well. I hope you see improvement quickly.
wow - that suck sand is awesome all in the same breath. It sucks that you and your family have to go through this, but it's great that you have such a head start on the therapy and a professional who has such a high hopes of a full 'recovery.'
H's cousin has a son who was diagnosed with autism at age 2 1/2. He started therapy right away and is now 8. He continues to see someone and does have a few 'ticks', but he is in main stream school and will hold a conversation with almost anyone! He has made such amazing strides and is so very smart. I personally feel that he wouldn't be where he is today without that early intervention.
GL to you guys!
I'm sorry- that's got to be tough to hear. But thankfully he's very young and getting help already which will help tremendously I'm sure!!
Refresh me- what things was he behind on at his WBV? What have you guys noticed?
Some of the things were that he "forgot" the words he used to use, he doesn't point, doesn't consistently respond to his name and doesn't communicate that well - like if he wants something he won't point, show us, bring us there, sign, grunt, etc. We just kind of guess. Eye contact isn't great, not affectionate (to some extent).
My little man at 0-1-2
Ah watermellons - I'm guessing you're feeling a mix of sadness at what the developmental pedi said but maybe a bit of relief to know you weren't just being an overanxious parent. Good to you and your H for pushing your fears forward and getting Brody some help.
Early intervention can really be amazing so I'm hopeful that we'll get an update from you in a few months about B's progress.
Creepy internet hugs for you guys

BFP #2 5/27/12. EDD 2/1/13. m/c and D&C 6/21/12.
It's so funny, I was literally just thinking of paging you this week to ask what was up.
Pretty much what everyone else said: it sucks and is good all at the same time. But hugs. I know it's hard to hear there is a problem. I really hope everything is looking up from here on out.
I'm sorry to hear you're dealing with this, but I'm happy that it sounds like he'll be getting the support he needs. One of my best friends has two sons who are on the spectrum and having a good therapist has done amazing things for them...not to mention helping my friend understand how to communicate with and help her sons better. I hope your results are similar.
::big hugs:: and wishing you and DS all the best of luck on the road ahead!