Having kids on medications is always a work in progress. Our four older kids were rarely on any type of medications except for the occasion when they had an ear infection or something like that. This was never an issue until we began to do foster care. Many of those kids were on medications. For our special needs kids it is a must and adjustments are just a part of the process as they grow and change quickly. We have kids on meds for everything from seizure disorders, sleeping issues, hyper-activity, anxiety, etc, etc.
It is not the best time of the year (usually we try to change meds when there is no school), to adjust Hanna`s meds but we have to. Her behavior is just so awful, she is not sleeping even on massive amounts of medication, and she has grown. She will be taken off everything and then we will start over. It is not easy to make adjustments when the kid is not able to tell you how they are feeling and what they think is working. In Hanna`s situation she does not care what she is behaving like, if she is acting really weird it does not seem to bother her, or if she bothers or hurts someone else along the way is of no concern to her. We can only observe and make or best judgement from those observations.
The next couple of months might be a rough and scary ride so hang on and get prepared.