(Note to self - Make sure I frequently read Ed's blog to check on what he is saying about me!)

Well things have been quiet at the Peck household. Just the way we like it. Ed had an oncologist appointment on Monday, and his blood work determined that his "light chains" (defective protein levels) still continue to improve. The Dr. prescribed another two weeks of medication and chemo.
Although his pain level is down - he has his good days and bad days with fluctuating pain and energy levels.

Unfortunately a major side effect to his medications is the fluctuation of his blood sugar.
As soon as we were rejoicing about his protein levels - the doctor called concerned about his high blood sugar level. Again - we can NEVER let our guard down! Back to the General Practitioner for another new medication.

So far Ed's stem cell transplant process is scheduled to start on August 12th. That day he will have his port inserted. After that we will travel daily to Albany Medical Center for the first process of having his stem cells removed. Donna O., the stem cell coordinator, is sending us a daily calendar of what those next five weeks will entail.

We thank our beloved friends for their continued kindness. Ann & Sandy for the wonderful lunch - made with organic fresh veggies from their garden. Linda & Bill D. for the ice cream $$ they sent in a very funny card. Terri and Patty for the evening visit complete with an awesome pizza! Shout out to Valerie and Sue for bringing Ed over a gourmet lunch with brownies, and leaving enough for our dinner Thanks also for the continued cards, e-mails and facebook messages. Words cannot express our appreciation!