July 16 already and summer so far has been almost normal, we even went camping over the 4th!  The second round of Brentuximab was completed two weeks ago and it has been amazing: Faye has experienced some fatigue and nausea and her blood counts have been on the low side but wow what a difference from the horrible misery of traditional chemo. We just got back from scans at Childrens' Hospital and we are hoping, praying, crossing fingers, counting steps, holding breath, etc. to hear good news today. Things do work a little differently when tests are ordered from outside of the Hospital so we may not have any news until tomorrow.  If the scans are clear - or - 'clear enough' we will start to prepare for Faye's autologous stem cell transplant.  If the scans are not clear we will likely try two more rounds of the antibody.   So stay tuned, more later when we hear results.  ~Lolly