I received a call from Sick Kids Hospital today. It was Alan
George, the coordinator for the Cranio Facial Clinic. He called to tell us that
we can have June 21st as a surgery day if it works for us. He also
went on to say that Dr. Dirks, the neurosurgeon we saw was not available and
therefore we would need to go ahead with another surgeon. At first I was
concerned about this. I was comfortable with Dr. Dirks doing the surgery so I
was nervous about what he was going to say next. But then he told me that the new neurosurgeon
taking over Spencer’s case would be Dr. James Drake the Chief of Neurosurgery.
I was quite pleased. Alan asked me if we
wanted to meet with him first before setting the date so I then asked, “Do we
have to? If he is the chief, I am more than thrilled that he will be performing
the surgery and really do not feel the need to meet with him.” I’m very
reassured that Spencer will be in good hands with the Chief of Neurosurgery.
When I looked up Dr. James Drake this is what I found. Dr. Drake was born in London, Ontario, and educated at Princeton University (1969-1974), Royal College of Surgeons in Ireland (1974), University of Toronto (1986-1987), and Royal College of Surgeons of Canada (1987). Training included a research fellowship funded by the Medical Research Council of Canada (1986-1987) in Hydrocephalus. Assumed his appointment in the Department of Surgery, Division of Neurosurgery in 1988, and has been on the surgical staff at The Hospital for Sick Children in the Division of Paediatric Neurosurgery since then.
I think these credentials speak for themselves. So now we know, Dr. Philips will be doing the Plastics part of the surgery and Dr. Drake will be doing the Neurosurgery part of the surgery. Knowing that these doctors are both very capable, educated and skilled doctors eases the mind a little about what our baby is going to be going through.
After this part
of the conversation ended Alan George (the coordinator) went on to tell me that
he had some other bad news. Spencer’s blood is B +. I am A+ and Steve (my
husband) is AB+ which means neither of us is a match for Spencer and he will
have to receive blood from the Canadian Blood Service. This upset me a great
deal. I know that everyone says that the blood service is safe and reliable
however I do have my doubts. Unfortunately now we won’t be able to control what
he gets, we won’t be able to build up our iron to help him. We have to put our
faith in the “system” and pray that every drop he gets is safe and untainted. Alan
explained that if he gets either of our blood the “antibodies we have will
cause clumping and will do more harm than good” so Canadian Blood Service it
is.
We have two more appointments coming now. One is a CT scan which will be some time in May and an Anesthesiology appointment also to happen in May.
Other than all this Spencer is progressing amazingly well. He is such a happy, outgoing, energetic little boy who is going to be crawling any second! Can’t wait for the fun to begin when he doesn’t sit still for a second!
Spencer at 8 months |
Alana - is anyone else in your family a match for Spencer or can only immediate family store blood for him?
ReplyDeleteHi Anna,
DeleteThanks for your question. We have not tested anyone else in the family because Sick Kids Hospital does not allow blood donations from anyone but a mother or father. I'm not sure why this is and I will research the answer for you and post it soon.
This comment has been removed by the author.
DeleteHi Anna,
DeleteI asked Alan George the coordinator for the cranio facial program your question about other family members storing blood and this is the answer I received. "Limiting directed donors to parents is a decision of the Canadian Blood Services. The feeling is that family members may feel obliged to offer their blood when asked and not be completely open with respect to past sexual history or drug use."
Thanks for your question.