Hi My daughter didnt go on abilify after all as we decided to stick with olanzapine even though we know it takes time 3 to 4 weeks for them to work properly , but my daughter is very impatient to get rid of the voices or make them quieter.asap. Is there something that can speed up the process or at least keep her more calmer. be pleased if anyone can enlighten me, as its awful to see her suffering so much and feel useless to be able to help
29 May 2012
Atypical anti-psychotics, much like antidepressants take about a month to feel the full effects. I know it must be hard for your daughter. I also know this remark sounds a bit trite and is stating the obvious, but have you talked to your shrink to find out if there might be a little something to help her until the med takes effect? That's what I would do, but I drive my docs nuts, just me.
I'm sure some other responses will be forthcoming, so I'll sign off for now.
Peace and best wishes for your daughter and mom.
30 May 2012
There are some blanks that need filling in for me so bare with me for some questions:
How old is your daughter? Do you go to her psych sessions with her? What was the reason for choosing olanzapine over abilify? I am kind of surprised that there is no support group for your daughter. Did her doctor mention outpatient "group therapy" or other therapies of a structured nature that will keep her occupied?
Ativan can perhaps calm her down. But you need to discuss these things also with her doctor as Laura has mentioned to you. Just throwing out names of drugs for her to try isn't the best way for you to approach her doctor. Just ask the doctor if an anti-anxiety med is appropriate for your daughter who is "bouncing off the walls". See if that grabs the doctor's attention and see what the doctor recommends until her next appt.
I hope that helps you a little. I have done outpatient group therapy, too. Way back when something else was recommended to my husband and myself because the meds I was being put on would take too long to get into my system and I was... ummm, let's say, "over the edge and not coming back quick enough". But I wouldn't recommend ECT (shock treatments) for another human being as it has permanently wrecked my short-term memory. But at least it helped me during that horrible phase of my life until the meds kicked in. Be very careful what you ask her doctor for and be even more watchful and vigilant over your daughter as she is undergoing treatment. Whatever meds she is on do research on them so you know what the side effects are if anything adverse happens, you will know it and be able to accurately report it to her doctor. It sounds like you can have open discussions with your daughter so I would continue to do that and be her support system. This is probably scary for her, too as I am sure it is for you, too.
Can you talk a bit more about what is going on so that we can better help you and her??? We do want to support you the best way we can so the more information we have; the more knowledgeable will be our answers.
My very best to you and your daughter and hope to hear more from you soon.
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