16th March 2018

Just back from the Cancer Centre. We had a very encouraging meeting with Nick's primary oncologist. She reported that Nick's blood components (red + white blood cells) are normal, and he's good to go for cycle #2 on Monday. She also was overjoyed to hear that Nick's no longer coughing up blood, and is eating normally - strong indication that cycle #1's chemotherapy has been effective and is eradicating the cancer in Nick's lungs. We're overjoyed as well!

During the first hours of cycle #1, Nick had an anaphalactic reaction to one of the chemotherapy drugs, paclitaxel ("Taxol"). This is not uncommon, and there are prophylactic drugs that can be given to ward off such reactions. However, in light of Nick's breathing distress at the start of treatment, it was decided that this drug would be discontinued for the remainder of cycle #1. The plan is to reintroduce the drug during cycle #2, with all prophylactic measures in place, and start treatment early in the day so there are lots of staff around to deal with any adverse reactions. If Nick still reacts, then another chemo drug will be substituted - not an ideal situation, but probably not disastrous. 

It's such a pleasure to deal with the LRCC team - especially when they deliver good news. In our five years of working with them, they've never failed to embody the highest ideals of competence, compassion and professionalism. If there's one good thing about going through the cancer experience, this is it. Well, that and all the lasagnas. Thanks again all you bringers of fine comestibles!

Comments

Post a Comment

Popular posts from this blog

September 23rd, 2018 - End Game

I arrived at the cancer clinic at about 9:15 this morning, still wired after playing a great party in Bayfield, getting home at 2:00 am. Dr. Potvin had the results of the thoracic CT scan and the head MRI. The hope was that there might be on or two brain lesions responsible for Nick's dramatic neurological decline. No such luck. The cancer, grown chemo and radiation resistant, has proliferated in Nick's brain. There's no way to stop its growth, and it's ineroperable. Nick has days left. They're keeping Nick in hospital, as to send him home would result in horrific, traumatic consequences. The best they can do is try to make Nick's exit as peaceful as possible. Nick's six year battle is finally coming to an end. These six years have been trying, but we've not been without help, hope and support along the way. We love and deeply appreciate everyone who's had our backs during this time.
Read more

10th June 2019

Image
Last week we found out that the Nick Greeson Memorial scholarship had reached the $3000 mark.  On Friday, I spoke with two Humber representatives who told me that they were overwhelmed that we were able to raise that much money in such a short time.  "A remarkable achievement," Marlene announced. "We have enough money now to keep the scholarship going for another three years."  In November of this year, Matthew, myself and other family members will be attending the Humber Awards Ceremony where we will be honoured with the privilege of bestowing this award to another student who is/was struggling with medical issues while still demonstrating resilience and fortitude in the face of adversity -someone just like our Nick.  Thanks to all who contributed.  Please feel free to continue donating to this fund if you are so inclined.  We want to keep it going as long as possible. (LINK TO NICK'S MEMORIAL SCHOLARSHIP) I just received an email from a young man named Eri
Read more