Around 4 pm last Friday, heading into the New Year's Day weekend, I got a call from my nurse: we have a confirmed fully matched donor.
That is exciting news, although not surprising, Given that we had identified 65 matches, it seemed like a given that one of them would be confirmed. Still, it's a bit amazing to think that a random stranger, with no vested interest in my health or life, is going to donate their stem cells to me. I'm grateful that so many people are registered donors that the search for a match was as productive as it was. And of course, I'm grateful to this stranger whose stem cells I will hopefully receive in the very near future.
Who is it? Where are they from? When will it all get started? Good questions to which I don't yet have answers. I expect to have them -- or some of them -- this week as the scheduling begins, and so does the reality of the transplant.
I find my mind oscillating between fear and hope, between dark and light. There's the fear of the known - the risk of infection, relapse, and graft-versus-host disease; the social isolation and the myriad restrictions -- and fear of the unknown - how will I tolerate the chemotherapy conditioning, the actual transplant? What will my daily life be like for those first 100 or so days? What will it be like after it?
The Shed, after hours of assembly, site preparation, and a short move across the lawn to its final location |
This past week, the holidays brought with them some time off work. Not only did I get to celebrate with my family, but I also got to tackle a few projects - including the building and siting of a new shed in our backyard. It took many hours of assembly, of trips to Lowe's to prep and level the site where it sits. And then today I spent a good chunk of time cleaning out the garage to take advantage of said new shed. Not exactly a day of fun, but accomplishing something, being productive fills me up. On top of it, I even got in a short pain-free run that was a lot closer to my normal pace. It was a very good day.
The moon tonight, shining through the clouds |
I found your blog during my own treatment for fNHL which had developed into bulky tumor in my abdomen in 2012. I used to get an email of each of your posts and then they went down to one a year and then they stopped. I mostly figured that you were doing so well that blogging had become superfluous, but the possibility that they had stopped for a more dire reason niggled at me.
ReplyDeleteAs a recent scan of mine came back with some features that need further investigation, I decided to track your blog down, only to find that I had missed all of the 2022 activity. I am sorry to hear about what you have been going through, and I am grateful for your generosity in sharing your story. I think of my lymphoma as something of a housemate that I need to be able to get along with in the same domicile. And I remind it, "Don't go all Pacific Heights on me now."
Wishing you all the best with your SCT and imagining you taking many happy runs in your future.
Thanks for the comment. I did kind of stop blogging when life was status quo and I didn't really have anything to say. Unfortunately, that's changed but I'm keeping positive (mostly) and hoping that we will get back to boring updates eventually when we are on the other side of SCT and recovery! Wishing you the best with your fNHL and hope it remains a very quiet housemate for you for a long time. -- Michael
ReplyDeleteI had to go delete a few comments that were posted here as they were rants about the quacks and conventional medicine and blah blah blah. They could have been bots or they could have been real human conspiracists. If it's the latter, I'll keep deleting any comments that venture into that land. They don't belong here.
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