Keri,
As one who has never sought the services of a developmental pediatrician, and also lives in Los Angeles County, I have been extremely happy and thankful for the services we have received over the past six years. I know of several other posters on this site from California who would say the same. I cannot speak from a biomedical standpoint, since it is not an area I have ever explored, and if that is what you are looking for, then the above member may very well be right, but if it is school district services you are asking about, which is the impression I got from your post, then I think you will find that California is near the top of the list, though it may fall just a bit below New York, which from what I understand is the best. What we do have to offer, which no other state has is Regional Center, which provides a myriad of services for individuals with developmental disabilities. Generally you will find that what the school district doesn't provide, Regional Center does. The real biggie here is that they pay 100% for social skills therapy (with a Regional Center vendor, of course
Also, I have been very happy with Los Angeles Unified School District, though it was a bumpy road for the first few years following our diagnosis. Like most SD's, they will attempt to take advantage of what you don't know if makes dollars and cents to them. Once I went through the mediation process, though, I have found the going a lot easier. Not only am I much more familiar with my rights, but they recognize that I am not someone they can take advantage of, and the relationship has been much more mutally rewarding
Hi, Keri. Not to put a dark spot on some exciting plans, but if you're counting on California being as progressive as the northeast in autism programs, you might be surprised, especially based on the big talk schools tend to standard-issue out to parents about how focused they are on each child's individual goals, yadda, yadda (I'm pretty sure they all get it from the same script).
I'm in about as progressive an area of CA as can be--in Los Angeles County--and believe it or not, I have yet to run into a single professional, including STs, OTs, special education teachers, school principals, pediatricians, our neurologist (I sh*t you not) AND EVEN Blue Cross/Blue Shield of California, who have even HEARD OF a developmental pediatrician. ETA: No, wait. That's not right. I remember that our neurologist had heard of this but didn't personally know any recommendations, and our former OT knew about them because she read about them in a book (might have been "Daniel Isn't Talking," I don't really remember now).
Maybe my experience was unique but I tell you I grilled every professional I could drum up for four solid months of several-times-a-week phone calls to attempt to unearth a single developmental ped and apparently nobody has...heard of one. Sigh.
I don't know about New York, but New Jersey is typically rated among the top states for autism awareness in education and in accesibility of programs. Are you sure you guys want to move?
Property taxes will be a little lower here. On your significantly higher-cost-for-the-same-size house. So it's six in one, half a dozen in the other. Let's not also forget that sneaky little tiny 8.75% sales tax.
I'm not saying don't move to CA. I noticed you want your husband to work shorter hours and frankly, no matter where one decided to live, including the moon, that would be HUGE for a special-needs family. I know because my husband now is gone from the house 12 hours a day (here in CA)...because of that tiny little 3-hour-daily commute so that he could get a job that would pay parallel to the northeast, but be in a house that was *less* than 0K for two average or three small bedrooms...I'm sure you're getting the picture here...
It's not all roses.
The weather is nice. Not having seasons sucks, sucks huge. The people are really nice and cashiers pack your bags for you and ask if they can help you out to the car with them, even if all you bought was a light bulb and a carton of tampons. People tend to be very polite. Bear in mind that I'm not in the city. I don't know how polite other areas might be.
Whatever you decide, good luck, and again, not trying to dissuade you; just letting you know that *some* (not all!) of what you're seeking here won't be as easy to find as you might think. Of course you *can* get services, etc. I have found that, by comparison to family members and one friend I know in NJ, it has been exponentially harder to do so here in CA than the time they're having over there. Also, depending upon the school district you're in (we're in the Bonita school district even though we don't live in that district because of a special program), the school might describe to you various programs and various models (ABA, TEACHH or what-have-you) but once you're standing there in front of them with your child fiddling with his Pull-Up and you nervous and your husband with big hopeful eyes, they might say "Oh, this won't serve your child's needs" and it will take you 12 months, 100 phone calls, a lot of tears and a lawyer to figure out why...much less pursue it more actively).
You'll get the basic services, of course, as quickly as you would get them anywhere else. You may find like I did that no matter what your child's cognitive level, speech development, amount of/degree of/amount of time spent on stims, seizures/no seizures, missing arm, three arms, no head, was originally a Martian, etc. they will invariably tell you (at least around here) that you're going to "start out" with "standard" ST of 70 total minutes a week, "standard" OT of the same and "the most FANTASTIC class, it's PERFECT for your son" which will invariably be the cookie-cutter-issue SDC class. My son's SDC class included children with "severe" autism, "mild" autism, no autism (one child diagnosed with apraxia of speech and no additional diagnosis), a child who did not have autism and was born with a chromosomal uniqueness but hey, he wasn't speaking as well as an NT child so throw him in there too, because a delay is a delay, right? It leaves you kinda wondering if a child were born with no tongue, would he also be shuffled to this "fabulous and perfect!" (and, by amazing coincident, cheapest at the local level and cheapest at the public school level) class because he wasn't speaking very well...
I think you're getting the general idea here. You can get *services*, you just might have to kill yourself trying to go crazy with, I don't know, two full hours of ST a week or something totally crazy and extraneous like that. I know my frustration is showing in these posts...but if I could do it over again I would not have moved...so I can't help but put up the warnings here for another special-needs family...though again, CA is a big state and I don't know what part you're planning on moving to. Here's a place where you can get lots of specifics on relocation and first-hand experiences: city data forums. I don't know if we're allowed to post URLs here but if you Google that you'll find it right away.
So in summary, services *can* be had, you just have to fight like a dog to get them. PM me if you want specifics. Not trying to talk down CA. Depending upon where you live in the state (it's a huge state!) it can be very beautiful here and there are lots of things to do. (I live in the San Gabriel Valley, in the suburbs. Next to San Dimas...home of Bill and Ted! A severely underrated movie.) Watch out for the smog index, though. (Okay, I'll stop.)
MyDear, I'm sorry you haven't had a good experience with California services. This has not been the case for me. Perhaps because my son was diagnosed when he was school-aged? Many of the services you mentioned are those that we have never asked for, simply because my son was too old, and had already progressed beyond that need at the time of his diagnosis. As far as Regional Center goes, it is worthwhile to note that not all RC's are the same as far as their willingness to take on a client, and quality of service coordinators. I'm with North Los Angeles County Regional Center, and they are fabulous. I've never had to fight for anything with them, and I've got a high-functioning Aspie. My sister, on the other hand, lives in the South Bay, and my developmentally delayed, epileptic nephew has been declined as a client! Go figure. It should be the other way around, but here we are
As far as school services for the OP's son, his existing IEP would have to be implemented until he is up for his annual IEP. At that point, it is conceivable that the new team may not agree with the services provided in his previous IEP. The only defense for this is to thoroghly research all the school districts in the area you are considering moving to, and to even go beyond that and research and visit the schools as well. It all starts with the school. Believe me, I know from experience. I made a point of staying in the the Los Angeles Unified School District when we were looking to buy a new house, because all my research told me to stay away from small school districts with shallow pockets. They will fight you tooth and nail to not spend money on your child. LAUSD will throw money at you if you know what you are entitled to and don't let them get away with pulling any crap, which they will try to do! You can't walk around with your head up your you-know-what. You've got to keep an eye on them, and jump in with a "Hey, you can't do that"! Every time I have done that, they have folded like a house of cards.
California is not a utopia for autism services. No state is. But I have found from personal experience, and the consensus of this board, that it is better than most. Again, I am sorry that you have had such a rough time. Move to the north San Fernando Valley! Every parent I talk to here is very happy.
Never mind. To the OP: good luck with whatever your decision is! Wishing you happiness wherever you wind up. You have been given some anecdotal information here and the rest is really up to you as far as research. You can PM me any time. Good luck![Edited out due to to Administrative reasons and at the poster's request]
Please note that this post was made at the same time that the thread was locked by another mod. Neither party had any way of knowing that one was posting while the other was locking.
We apologize for the inconvenience and hope to see no more flaming.
The Regional Center handles the special services a state is *already required* to provide if your child shows a certain degree of delays in given areas. *Anything beyond the absolute norm* that *most progressive states provide* is expensive and you will be dissuaded. For example, our kindly but absentminded (due to a stroke) service coordinator at the Regional Center is the one who finally got tired of my phone calls about ABA (and tired of remembering that she still forgot to even submit the paperwork for the IEP we had about it...months and months and months prior) that she at last stated to me that by asking for "additional" services (such as ABA), I was "basically telling C that (I) don't accept him" and that "that in fact can be what holds a child up from developing". After that phone call I dropped ABA. One year later this same woman called me to ask me *why I hadn't followed up further on ABA* and that it was *such a shame and pity because now they considered C "too old" and "beyond" ABA, so...oh well.