tag:blogger.com,1999:blog-5123456984059720316.post65886073273538936..comments2023-10-17T07:38:00.727-07:00Comments on Kevin and Barbie -- Our Journey of Hope: Feeling Betterkevinandbarbiehttp://www.blogger.com/profile/04634011893927790997noreply@blogger.comBlogger1125tag:blogger.com,1999:blog-5123456984059720316.post-59490533358705647852008-11-06T02:55:00.000-08:002008-11-06T02:55:00.000-08:00Hi Kevin, well you can see what time I'm writing t...Hi Kevin, well you can see what time I'm writing this post (2:30AM). Can't sleep could be the Decadron I took yesterday, otherwise feel pretty good. It is so funny that your post had something to do with "Life". My last post was a poem called "Life", which says, Life is not measured by the number of breaths we take but by the number of moments that take our breath away". We continue to connect in so many ways. I'm looking forward to the Amyloidosis meeting on Saturday. I have email Dena and she does have some interesting information especially about the support group back east. I'm glad I didn't involve myself. Hopefully, this support group will be just a wonderful as the heart transplant support group in Santa Clara. When did you first feel the side effects of Decadron the first time you took the drug. I think you said by Saturday. My cloyshorine count went down from 311 to 237. Still a good number but hopefully it won't drop further before biopsy on Tuesday. See you on Saturday and hope all is well. Tell Barbie hi and we miss you both. love debbie douglasAnonymousnoreply@blogger.com