Anonymous wrote:PP with the AB 1424 form.
It certainly can't hurt to complete it just to have on hand for your own documentation -- then maybe pass it along if the police or care team seem open to receiving it. I know my son wasn't/isn't in a headspace where he can tell anyone what meds he's tried, did they work, where/when he's been hospitalized. And if he doesn't authorize anyone to reach out to us, they'll never know these details that are so helpful in a crisis. Sigh...
Anonymous wrote:PP with 22yo son here. I can open my own form but for the life of me can't track it down on my own county's website. In CA it's called an "AB 1424 Form" and a lot of counties use the same one, like this:
https://docs.google.com/file/d/0B1mjz02FtuU_UGc3VWxjQ2pjRzg/edit?resourcekey=0-ENvwYqyhSvmidQKZQybLdA
My own county has what I think is a better form and I'll keep looking for it and will post it when I find it.
Sending virtual support to anyone going through this. It's brutal. Our son finally called us yesterday, after 5 days of being MIA in the system. So at least we know where he is. So hard.
Anonymous wrote:I found with the last round of hospitalizations (2 involuntary hospitalizations at three different facilities - there was a transfer partway through one) that staff would not even accept our calls after my kid said no contact and they would not provide the staff and doctors names so we couldn’t actually even share information. We couldn’t even share medication information or outpatient provider information.
Oof. I get it from their perspective since what is happening is very real to them, and of course HIPAA rules are there for a reason, but it's still so hard. Mine will talk to my husband but I am barred from contact for whatever reason. As a mom, it's really hard. We're on the third hospitalization but second facility, so our hope is that they can review last year's records for some sort of baseline.
We're living two lives right now; our younger kid is about to graduate from HS, going to the prom this weekend, very excited for a trip with friends this summer, moving across the country for school in the fall -- and then have all of this going on at the same time. Cosplaying a happy family is exhausting and we get to do it all weekend for a visit from elderly extended family who will not understand our situation or think that heavy application of prayer or organic vegetables will cure everything. We live in a really gossipy community and I know we are a topic of conversation. I feel so deeply for everyone here who is going through it; it's a lonely existence.
Anonymous wrote:
If he said he was ok, what made you think he wasn’t?
I found with the last round of hospitalizations (2 involuntary hospitalizations at three different facilities - there was a transfer partway through one) that staff would not even accept our calls after my kid said no contact and they would not provide the staff and doctors names so we couldn’t actually even share information. We couldn’t even share medication information or outpatient provider information.
Anonymous wrote:Just found it -- it's actually the same but their letterhead makes it look nicer. Anyhow! I do think it's helpful to give to a care team, particularly in a situation where your loved one isn't able or willing to communicate medical history etc. With HIPAA, a care team may not be able to talk to you, but you can pass information to them.
Anonymous wrote:Another parent of a kid who became psychotic as a young adult (21). The forms are a great idea. It’s not foolproof because we found hospitals still ask and my kid refused to allow us to get information and I can’t tell you how hard those periods are when you don’t know where your kid is.
Anonymous wrote:My 22yo had a psychotic break 18 months ago and it's been incredibly hard to pull him out of the psychosis. Currently on his third hospitalization/psych hold. We wish SO SO much we'd been a lot stricter in high school about him smoking pot. I think that was the gateway to everything that came afterward and it has such strong ties to psychosis. It seemed like this came out of the blue, but in hindsight there were signs of what was coming. However, we didn't know what to look for, or that we should be looking. We have no family history of anything like this. It's a living nightmare and something I wouldn't wish on my worst enemy.
The only piece of advice I have is to try to get your child to sign a release enabling you to speak with their medical care team once they are 18. We didn't have this in place and it made things so much harder. We couldn't get him to update it and have just been told it expired.