Sunday - January 26, 2014
Thursday was a full day of medical appointments - bouncing around between 2 UCSF campuses. Appointments focused on my lifelong inability to shake coughs/colds, the continuing mystery of my elevated liver enzymes, my (improved but extant) gastro distress, and of course the specter of stage 4 DLBC lymphoma. So while I am very happy to have a new game plan to address my persistent colds and am relieved to put off a liver biopsy for at least another month, I am most contemplative about my conversation with my oncologist.
The urgency of VCU's Bone Marrow Transplant plan hovers uneasily above my current health, undermining my piece of mind. VCU and our second opinion at UMD placed such an emphasis on securing that allogeneic BMT. I was even considered for an NIH clinical trial as a means to get me that (dangerous) life-saving BMT. But no match came off the Be the Match registry. And it turned out that I was NOT eligible for the NIH trial (because I had not relapsed - thank God). My last option was a mini-haplo at John Hopkins where the lymphoma specialist said I should not undergo a BMT unless/until I relapsed. UCSF strongly concurs with Hopkins.
My oncologist emphasizes that statistics are my friend. As every month passes without relapse, my odds improve. As noted in yesterday's wrenching article in the New York Times, "these survival curves, called Kaplan-Meier curves, are one way we measure
progress in cancer treatment, plotting the number of patients surviving
over time." In my case, the greatest chance of relapse is (was?!) in year 1. I am acutely aware that I am certainly not out of the woods. I am semi freaked out every time I awake slightly damp or feel tired at the end of the day. Can you imagine my angst if I ever got a headache? Particularly on my left side? However, the radiation of the PET and MRI scans carry their own risks. What to do? Well, given statistics, we are going to wait until April vacation for my next round of scans. We are going to wait for 6 months rather than our previous 3 month interval. And I am going to try to shake the worry and those jangled nerves.... Focusing on the positives of my health.... Being mindful of my many continued blessings....
Sunday, January 26, 2014
Monday, January 20, 2014
A Wonderful Month
Jonathan birthday gift unwrapping (in the ER) |
Today is the official end to our fabulous month of our winter holiday and simply being together. I've just returned from driving Megan back to Davis, Jonathan left for his final semester at Virginia Tech on Friday morning, and Joe and I will now recalibrate and return to our comfortable empty nest routine. Our month was marked by explorations of Marin, lots of fabulous meals around town and at home, movies, board games, and of course much cuddling with the hounds and watching sports. Much downtime, lots of hanging out, with Joe taking time off work and me succeeding in holding off lesson planning for large swaths of time. Jonathan hunkered down on the living room couch as we stretched the limits of our tiny apartment above the bay. It was all worthwhile. Who knows when we'll have this luxurious block of time to relax and spend time together?
We wrapped up our month with Jonathan's 23rd birthday celebration on Thursday. With Megan coming back from Davis to share the day, the kids went into the city for a meal and movie (while Joe and I worked) and then returned to Sausalito with the plan for dinner birthday festivities. However, it's good to be flexible and - long story short - we ended up unexpectedly celebrating Jonathan's 23rd in the hallway of San Francisco General's ER. This surprise diversion was just a precautionary observation of Joe and some extant issues yet it still raised the adrenalin. And an inner city ER is QUITE a scene, giving us ample reasons - once more - to be grateful for our good health and connection. All's well that end's well. A birthday to remember :) A month to cherish.
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