In January 2011, my wife Nancy Jones was diagnosed with leukemia.
This is the story of our journey, told through email updates to our
family, friends and community.
Wednesday, December 28, 2011
Cremation today (day 7)
Monday, December 26, 2011
Ritual unfolding (day 5)
Om tare tuttare, ture soha
-tdc
Sunday, December 25, 2011
Healing through dreams (day 4)
I'm in a hospital, and I've been there as a patient for a very long time. I'm very weak. Some friends come to visit, and they tell me I can get out; they bring light-colored clothes, help me dress, and start me on a journey out of my room. I follow their instruction, go down the corridor, down an elevator to the ground floor, heading towards the outside. I encounter a few medical staff, who ignore me, and a patient in a hospital gown, who looks at me in pain, as though she is stuck inside her disease process, and recognizes that I am not.
On the ground floor, it gets lighter and lighter as I get closer to the outside, and natural daylight starts to filter in. I go through several unmarked doors to head in the right direction, until I finally open a door to full bright daylight. It's a parking and delivery area behind the hospital, but the light is so bright I can barely open my eyes.
I'm in UCSF hospital, walking through the ICU to visit Nancy. When I get to her darkened room, and slide open the door and the curtain, I do not see her or any of the medical equipment or bed. Instead, I see a row of candles, small lamps and colored lights beginning in the middle of the room and vanishing into the distance and the darkness, like an infinitely-long strand of the best Christmas tree lights you can imagine. All the lights are different, and they are close together, so the lights merge and become a straight line of never-ending color.
Nancy Jones and I are in a small rustic wooden structure, something like a cabin on a large lake somewhere. There is a small number of other people there (maybe 10 tops) but no one from outer life. The mood is happy and comfortable but not raucous, joyous or overly celebratory. It feels like a group of friends getting together for no particular reason. Nancy is dressed as she often was when we were in the MS together – white t-shirt and black tights.
A time comes when Nancy wants to leave but, for some reason, she does not want to use the door. Instead, she wants to go through an opening that looks like a small window with no glass in it. It's about maybe 12-15 inches square and is about the height of a decorative window that you might find in a door, maybe 3-4 feet off the ground, but it is in the front wall. I quite frankly don't think she will fit through it and tell her she should use the door but she insists and does get through the window. I also get outside but don't really know how I got there.
Outside there is a small boat, like a rowboat but with a small gas outboard motor. Nancy doesn't know how to handle this boat so I have to teach her how to steer and how to use the twist throttle. We go together in the boat as I teach her how to do this. Although she has never piloted a boat before she picks it up very quickly. We motor over to something that looks like a small breakwater made of concrete that curves over to the shore. I get out of the boat on top of the breakwater and Nancy takes the boat and heads out into the lake.
Thursday, December 22, 2011
Continuing our prayer ritual (day 1)
From Tara's heart rainbow, light shines forth throughout the six realms and the bardo,
enveloping the deceased one, Nancy Jones, wherever she is,
purifying her karma, and infusing her with Tara's radiant blessing.
Her form becomes brilliant spheres of light and dissolve into Tara's heart-mind,
a realm beyond the cycles of suffering, a realm of absolute purity and bliss.
-tdc
She's gone (day 57)
-tdc
Wednesday, December 21, 2011
The limits of endurance (day 56)
Even before I got here today, Nancy was deep in conversation with our friend Tina Benson, who married us just over five years ago. Nancy has had enough. Enough treatment, enough hanging on in the face of a hopeless situation, enough discomfort and indignity and medicine and treatment and handling. Babbas Andreadis got here around 5:30, and talked with her and separately with Tina and I. Nancy's choice is clear, to all of us. Those of you who know Nancy well also know how decisive she is.
So we have changed her treatment completely. She's been breathing on her own with pressure support for more than a day, so the change was pretty easy and gentle. She is now medicated to handle all pain and anxiety, and is back on a trache collar, breathing air for herself. She's not getting any more antibiotics. She is dozing, able to hear us,and looks completely relaxed and comfortable as Tina and I sit vigil with her tonight. I've called her family, and I expect they will be visiting soon.
Please pray for her peace, send her your love, remember all that she is, and cherish her. We expect her to slip away sometime soon, perhaps tonight, perhaps tomorrow.or the next day.
I had a white light dream last night, and now I know why. I've told her again how I love her very much, that I chose her. I pray to be fully present for this, and for her to find the love she has always doubted, to join the light I dreamt of. We hold her in our hearts, and wait.
Love,
-tdc
Tuesday, December 20, 2011
Change in the air (day 55)
-tdc
Monday, December 19, 2011
Restoration (day 54)
The friends who have been sitting with Nancy at night all have feedback and suggestions for making it easier for her to sleep, ways to make her more comfortable. And the medical team has been really good at taking the feedback and turning it into standing orders that should make life easier. For example, instead of moving her every two to four hours (standard protocol to avoid bed sores and pneumonia) they are going to give her a good dose of pain meds at 9pm, reposition her a half-hour later when the pain meds are in effect, then let her sleep until she wakes. She's slept a lot today, and apparently rested pretty well last night too.
And it's a good thing, as her fever is back. She's currently running close to 102°. She's not agitated or trying to talk much, with a fever like that. Her nurse just brought ice packs, and gave her some tylenol, so it should come down some. We don't know if this is the abscess, a new infection, or some neurological effect. I remember a few months ago, when a temperature like this would really have me freaked out. Now, with all we've gone through, I'm just taking it in stride, and trust the medical team to handle it. There is a lot of competence in this ICU, and I never worry about the level of care she gets.
I feel rested after 10 hours of sleep last night, and I'm functioning a lot better too. I was able to get a bunch of bills and things handled this morning, stuff I just couldn't cope with last week. Today was also a good productive day at work.
Our community here is turning out to be amazingly resourceful...one friend with training as a speech pathologist suggested that we should look into electrolarynx technology. This is a hand-held sound device that you press against your throat, allowing someone who can move their lips and tongue to talk. I called the UCSF adult speech therapy department today, and they are arranging a consultation. But in the mean time, I've found some models on line, and am ordering one tonight with overnight shipping. With a little luck, Nancy will be able to talk on Wednesday. She will sound pretty robotic -- the sound these things make is not very human -- but I expect that the ability will be welcome. It's going to take some training and practice to make it work, but I'm sure several of us who are often with her will be happy to figure it out.
There are a number of new folks on this list, so I'm putting my older emails out into a blog, where you can read some of what has been happening up until now. Right now I only go back to late November, but in the next couple of days I will try to get the entire year out. You can see the blog at http://nancyjonesupdate.blogspot.com/
Janet is spending the night with Nancy tonight, and I think we have a full calendar of folks sitting with her over the next two days. More have joined the caregiver list today; I think we're up to nearly 30. I really appreciate this support. It's time to head home for dinner.
Love,
-tdc
Sunday, December 18, 2011
Against the wall (day 53)
I am attentively sustained by the profound presence of all buddhas.
-tdc
Saturday, December 17, 2011
On love and sadness (day 52)
-tdc
Friday, December 16, 2011
More rest and introspection (day 51)
-tdc
Thursday, December 15, 2011
A slight divergence (day 50)
-tdc
Wednesday, December 14, 2011
Resting into a new place (day 49)
-tdc
Tuesday, December 13, 2011
The hardest conversation, part II (day 48)
-tdc
Monday, December 12, 2011
The hardest conversation (day 47)
-tdc
Sunday, December 11, 2011
Winding down a bit (day 46)
-tdc
Saturday, December 10, 2011
A little progress (day 45)
-tdc
Friday, December 9, 2011
Somnolence (day 44)
-tdc
Thursday, December 8, 2011
A family reunion (day 43)
-tdc
Wednesday, December 7, 2011
Ritual Space (day 42)
-tdc
Tuesday, December 6, 2011
Our worst fears (day 41)
-tdc
Monday, December 5, 2011
Building community (day 40)
-tdc
Sunday, December 4, 2011
The Mozart Wait (day 39)
-tdc
Saturday, December 3, 2011
Two steps back (day 38)
-tdc
Friday, December 2, 2011
Back to the ICU (day 37)
-tdc
Back to ICU (early day 37)
-tdc
Out of the ICU (day 36)
-tdc