Real food symptoms and conditions

I took Prednisone for about 6 weeks for Stevens-Johnson Syndrome brought on by an allergic reaction to Ciprofloxacin. My main complaint on taking it was extreme hunger--not for sweets or junk, but for real food. I was also very moody and I think I must have been really mean to my husband. At the time, I thought I was being reasonable, but looking back, I can see I wasn't. It kept me awake, as well. Without the Prednisone, I might have died, because the extreme, constant itching with the Stevens-Johnson would have driven me completely nuts. My main complaint is that almost two months after quitting taking the Prednisone, I continue to have a moon face, facial swelling, and holding water elsewhere to the extent that I can hardly tie my shoes or even breathe. I would have expected that to get better by now instead of worse.

my 6yr old daughter was put on singulair at the age of 4 she had a reaction to nuts and had the allergy testing she was put on singulair and claritin and nasacort .(so she has been on the medication now for 14 months) about 3and 1/2 weeks ago she quit eating we had her to the dr several times they said it was all in her head that she could eat if she wanted to.she was then put in the hospital for 4 days they did the scope down the stomach found nothing i took her off all her meds because i didn't want her taking them with no food in her. she came home from the hospital and i put her back on the meds as the doctor requested and within 2 days she was crying non stop hitting me and telling me that she wanted to kill herself and everyone around her.she was putting her fists in everyines face and was very angry.she would cry and tell us that she didn't know why she was so angry.we took her back off of the meds because we were treating her for the stomach acid from not eating and within 4 days she was like a new kid.she is now eating ..happy ..and doing good in school..this is the 3rd time this yr on this med that she has quit eating we were told that it was all in her head .after reading everyones comments on here i called her doctor today and he said it could be the medication but they would have to put her back on it to check and i refused.no more singulair or clairitin for my children