<img src="i/expressions/face-icon-small-disgusted.gif" border="0"> My daughter is 15 months old and was diagnosed at birth with cf. I had to leave my job to care for her and am barely scraping by. SSI has denied Jayna because they say her illness doesn't cause her that much impairment. Between the chest pts, tobi nebs, albutarl nebs, ultrase, pecid, cipro, and genulose which we do daily(some twice a day) I think that is a major impairment on not only her life, but my own. How am I supposed to get a daycare to do all these treatments (they won't for cheap) and work? I need information and help caring for my daughter financially and no one will help!!! The state has me running in circles. Does anyone know the answer?