My husband and I have been dealing with Chronic Graft Versus Host since about November of 2004, and it is a struggle. I recommend therapy and talking to the doctor. My husband and I are handling it better together because of the therapy we have attended together and seperately. I wish you guys the best of luck and know that there is someone else out there that is going through this too... One of the best sites that I have found for information is the Leukemia and Lymphoma society site, which is www.lls.com, I am thinking this is the right site anyways. There is not a lot out there in the way of info, but the stuff you find is definitely worth searching for. Take care.