Hello again. Following up on my post earlier today with a couple of other questions....the day before our daughter L was hospitalized, we spoke with her psychiatrist, who said that the main reason for L to spend some time in a hospital or residential setting would be so that she would be in a safer and less stressful place while her providers tried a medication change. My impression is that she thought that L would be able to work on ERP and any other appropriate therapies while living at home (perhaps in a PHP) if/when her condition was a little more stable, and that we should be looking primarily to medication changes to get us to that point. Certainly at the moment it does not seem like she would be ready to deal with ERP now. What do those of you with relevant experience think about this? Certainly it will also be easier to find her a residential placement if we are not specifically looking for one with a specialization in OCD.
Another possibility is that she might go directly into a PHP without a period in residential. L says she at present would LIKE to have a residential placement where she would have less freedom to make bad OCD-driven choices, but she may have an idealized picture of what that is likely to be like. I'm struck that there seem to be a lot of bad reports about residential programs (although perhaps more about programs for teens with substance abuse disorders rather than adults with MH problems) and am somewhat concerned about her going into one, and especially if it is too far away for us to see her often.
On the other hand, three possible advantages of residential placement are that (a) if L's symptoms get even worse while changing meds, that could be overwhelming for my wife and me, (b) given the nature of L's compulsions, being in a residential placement would provide a significant level of "response prevention" even without explicit ERP--she would not be able to take herself to the ER or urgent care, she would not be able to check her blood pressure or O2 saturations repeatedly, etc. (We might be able to provide some of this if she is at home--e.g. taking Uber off of her phone, getting our BP cuff and pulse oximeter out of the house--but it would likely be more difficult and more stressful for us.) (c) more generally, as parents it is difficult for us not to accommodate or reassure L when she is in distress, even if we all know that this is bad for her in the long run--this should be much easier for care providers who are not family members. We'd welcome any thoughts about how much weight to give any of these considerations from anyone with relevant experience (or professional knowledge.) Thanks.