tag:blogger.com,1999:blog-22576999.post115806831963224567..comments2024-03-16T10:39:00.522-04:00Comments on Live With ME/CFS: Thrill of Victory & Agony of DefeatSue Jacksonhttp://www.blogger.com/profile/14532098225905355332noreply@blogger.comBlogger3125tag:blogger.com,1999:blog-22576999.post-1158192432100287072006-09-13T20:07:00.000-04:002006-09-13T20:07:00.000-04:00I'm so excited for Jamie! How wonderful that the F...I'm so excited for Jamie! How wonderful that the Florinef is working!<BR/><BR/>And you're sure right. This disease <EM>so</EM> sucks. Hope Craig's crash doesn't last too long. :(Michelle https://www.blogger.com/profile/05759387306193137795noreply@blogger.comtag:blogger.com,1999:blog-22576999.post-1158153330456360252006-09-13T09:15:00.000-04:002006-09-13T09:15:00.000-04:00It does suck! And I cannot imagine how hard it is...It does suck! And I cannot imagine how hard it is to watch your boys, especially when they are going through such different things. But Dr. Rowe is so awesome! He is truly one of the best doctors I have ever worked with. I am sending you good wishes.Anonymousnoreply@blogger.comtag:blogger.com,1999:blog-22576999.post-1158100625818708362006-09-12T18:37:00.000-04:002006-09-12T18:37:00.000-04:00I will keep your son in my prayers. I know how di...I will keep your son in my prayers. I know how difficult it is for us as adults to have to deal with this disease on a daily basis. For children, it has to be even doubly hard. Take care.Anonymousnoreply@blogger.com