Wednesday (9/30/09)

I know we sound like a broken record, as multiple times in this blog we have expressed our gratitude for your care and concern about our ongoing medical situation, particularly Bonnie’s. I (Steve) only need some hair (which is slowly coming in and quite noticeable with a magnifying glass), less sensitive fingertips and the removal of my “infusa-port” (in five months….ugh!) and I’ll be back to normal. Thank you for all your prayers specific to my situation.

Now for Bonnie. Yesterday we had a final consultation prior to her being admitted on Friday afternoon. She saw the oncology dentist, her physician and the pharmacist (who did an excellent job of explaining in a simplistic way the various chemo and meds and what can be expected). We were surprised and caught off-guard by one item that quickly modified our schedule today (Wednesday) and tomorrow (Thursday). Bonnie also has an implanted “infusa-port” that has been used for the IVs she has received since the initial 58 day tour at Sparrow Hospital. Unfortunately many of the “infusa-ports” have a smaller tube that restricts the volume of flow of blood product or other meds which can be pushed through so Karmanos has a special catheter (triple lumen) that is surgically placed. We also learned that this has to be done as an “outpatient” prior to being admitted in order for insurance to cover the procedure. The result is that we have to drive back to Detroit tomorrow (Thursday) morning for an 11:30 surgery, and then drive back to Lansing tomorrow night to turn back around on Friday for the formal admission. God is still teaching us to trust in Him no matter the situation, no matter His timing.

After being admitted on Friday, Bonnie will undergo five days of two different chemotherapies which will completely wipe out her bone marrow. This treatment is harsher than what she has already received, but necessary in order for the transplant. The actual transplant will occur a week from this Friday and will only take approximately 20 to 30 minutes for the stem cells to be transfused into her blood. The physical challenges will start to come into play the week following the transplant from both the side effects of the chemo and declining blood cells and platelets combined with the new stem cells wanting to fight with other cells in Bonnie’s body. We will use a future blog posts to give you additional information on how she is responding to everything.

Please continue to pray for God’s peace for us, as this is what has sustained us throughout the journey. Also pray for Bonnie’s protection tomorrow during the surgery to insert the catheter. Also continue to pray for Cassandra, Caleb and Callie as they will be apart from us for lengthy periods of time. It won’t be easy for them to jump in the car and pop in to see Bonnie, with Karmanos 1 ½ hours away. Thanks for your continued interest.

Blessings to all,

Steve and Bonnie