Anonymous wrote:Anonymous wrote:Anonymous wrote:DS was there last fall. It wasn't bad, but, I'm not sure how necessary/appropriate it was in our particular case. He needed to have his meds adjusted, and the doctors only wanted to do it there. So if the therapy was or wasn't effective, it is hard to know. That wasn't what he needed.
Communication was an issue. We'd drop him off then pick him up, but it took days and lots of phone calls to be able to talk to the doctor about a treatment plan.
And months later we are still getting bills. Although Dominion will tell you what the hospital part costs and what is typically covered by insurance, you have no control over all the doctors who see your kid, so 3 months later get bills from people you have never heard from who saw the kid. I'm sure this is typical for how hospitals work, but when you aren't the patient it is a bit harder to manage.
Also, for in-home, have you looked into going through CSA? That's the only way we were able to find in-home, since as you have seen, most programs (with the same providers) are for Medicaid patients.
What is CSA?
We are in Fairfax, so how it works likely varies by location. https://www.fairfaxcounty.gov/healthymindsfairfax/childrens-services-act
We went through school social worker, who sort of functioned like a case manager to bring together resources from the county and the providers. In the end, we had several months of services, from one of the groups that provides in-home. We scheduled directly with the provider, who invoiced the county. We paid a (high) co-pay and not through insurance for the services we received. But it seemed to be the only way to access that type of therapy.
Anonymous wrote:Anonymous wrote:DS was there last fall. It wasn't bad, but, I'm not sure how necessary/appropriate it was in our particular case. He needed to have his meds adjusted, and the doctors only wanted to do it there. So if the therapy was or wasn't effective, it is hard to know. That wasn't what he needed.
Communication was an issue. We'd drop him off then pick him up, but it took days and lots of phone calls to be able to talk to the doctor about a treatment plan.
And months later we are still getting bills. Although Dominion will tell you what the hospital part costs and what is typically covered by insurance, you have no control over all the doctors who see your kid, so 3 months later get bills from people you have never heard from who saw the kid. I'm sure this is typical for how hospitals work, but when you aren't the patient it is a bit harder to manage.
Also, for in-home, have you looked into going through CSA? That's the only way we were able to find in-home, since as you have seen, most programs (with the same providers) are for Medicaid patients.
What is CSA?
Anonymous wrote:DS was there last fall. It wasn't bad, but, I'm not sure how necessary/appropriate it was in our particular case. He needed to have his meds adjusted, and the doctors only wanted to do it there. So if the therapy was or wasn't effective, it is hard to know. That wasn't what he needed.
Communication was an issue. We'd drop him off then pick him up, but it took days and lots of phone calls to be able to talk to the doctor about a treatment plan.
And months later we are still getting bills. Although Dominion will tell you what the hospital part costs and what is typically covered by insurance, you have no control over all the doctors who see your kid, so 3 months later get bills from people you have never heard from who saw the kid. I'm sure this is typical for how hospitals work, but when you aren't the patient it is a bit harder to manage.
Also, for in-home, have you looked into going through CSA? That's the only way we were able to find in-home, since as you have seen, most programs (with the same providers) are for Medicaid patients.
Anonymous wrote:My son went to the PHP program for HS. It was awful I am sorry. I know gettingin there is quicker, but look to other programs like the Kellar Center.