I believe that these can be signs of oversuppression.  But lately I believe that most of these problems are because of substandard treatment.  Our children have a right to the best quality care possible with the technology that's here.  This is why I want a time released hydrocortisone pill.  It could be given before bed and not released for say 7 hours when our children need it.  Too often, the HC is given only 2 or 3 times a day and at the wrong times (big dose at night).  This is very inefficient in suppressing the androgens.  Because of this, the amount of HC needed  to adequately suppress the androgens must be increased.  Then, the signs of oversuppression happen when maybe the numbers look right but other things aren't.  This is why, with our endo's permission, we have begun a new regimine of when and how much HC to give.  (See previous posts under good news and slow growth.  Weight gain, moodiness, short stature, moon face, osteoporosis, headaches...these can all be side effects of too much HC.)  I am truly sad that there is not better treatment for our children.  I am also mad!!  Why do we accept this?  We need to join forces and demand quality treatment for our children.