My Granddaughter has been on the Liquid suspension 1 mg 3 x a day. What are the crappy things you have heard about it ? She was diagnosed at 13 months and is now 3 and 1/2. She does not eat very well... as a matter of fact she hardly has an appetite. We have to make her eat. She was on 1 1/4 mg and last visit they changed her back to just 1mg. Said she was ding TOO WELL. Not sure what that means... but we are in the thought process that less medicine is better. She takes it so easily and does not mind taking the liquid. The florinef we crush and put it in juice.  I could use any feedback on the pros and cons of this also. Thanks Cherry