I have now been on Valcyte for 13 weeks and have just started my first week back at work. GI symptoms have decreased considerably. Decreased fatigue. No headache until today. Mild swollen glands and sore throat. I am concerned because I just received a disturbing call from the short term disability case manager who states that they have denied my claim. They have been a pain to work with as well as my CFS doctor. I have been very emotional today since hearing this news. Does anyone have increased difficulty with emotional stress while on Valcyte? I am so fearful of a relapse due to the emotional stress. Any ideas on how to handle emotional stress while dealing with CFIDS?