This
Thanksgiving week I am in Florida, sitting in a Hospice center with a dying
friend. As many of you know, tending to the needs of a loved one who is nearing
the end of life is a blessing and an honor.
But it can also change quickly into feeling like a curse, depending on
the levels of fear, anger, denial, and pain being experienced by the person coming
to terms with their dying.
The day
before yesterday was a good day. From the moment I walked into the room where
my friend lay, until I left several hours later, there was a feeling of lightness
in the room that was not there the day before, nor the day after. As I entered,
S raised her head and smiled
angelically in greeting; the dark imprint of fear and anger that was there the
evening before erased from her features. We connected in ways that I’d hoped we would again
before her passing: quiet talk of shared memories and pleasant camaraderie,
even a few moments of honestly facing the facts of her demise as we discussed the slowing of bodily functions, the body’s
way of shutting down and bringing closure to life in the here and now. There
was an air of peace that felt like sheer Grace as we explored this letting go as
I gently rubbed her feet. Gone for the moment were the usual feelings of intense
panic, anger, and sadness over her multiple losses of personal control, unfulfilled
dreams (she had never written that book she had meant to write), and having to leave all that is dear to her
in this life. Not that I judge those
feelings as bad. Who wouldn’t be thrown into despair
when facing a dread disease like cancer? But, thankfully, while it has ravaged her
body and at times darkened the thoughts of my friend's mind, cancer has not destroyed her
beautiful spirit.
Just hours before this day of blessing, I was wondering what
I personally could do to brighten S's remaining days; to make her last
hours memorable. Intention sent. Problem
solved!
That morning I walked in to my friend’s Hospice room to find her not
only more lucid than she had been in a while, but infinitely more cheerful as
she asked if I would read to her from the newspaper (it had been weeks since
she had shown any interest in the outside world). Disregarding everything except the editorials she loves, I read to her while she smiled and
dozed happily on and off. Later, she shared her fear of being judged by her
Hospice caregivers when she couldn’t perform simple functions like going to the
toilet and holding her own glass of water. Being in Hospice care is an exceptionally
vulnerable position for my fiercely independent friend to be in. She, who had
chosen to never marry and who had earned her Ph.D. in psychology as a young
woman with little help from her own dysfunctional family, had not relied on
others for much physical or emotional support in her adult life. Once out in
the open, her concerns about being weak, needy, and insignificant, as well as her
fears about the Hospice staff, didn’t take long to resolve. This helped her to
move on to her biggest challenge: moving through the process of physically dying.
Blessed day! She really seemed to grasp that it was time to let go and let
others lovingly care for her as she had done in her counseling practice for so
many others.
Ah well, that was then and this is now. Today is not such a
light-filled day. But S is not back at
‘square one,’ not by a long shot. She has spiraled up to a higher plane as she
circles back to confronting her fears, anger, sadness, and loss of control. As
they say in the 12-Step Program: one day at a time. And as I say at times like these: one minute at
a time. Each step forward reminds me as a caregiver to give thanks for those
special moments of grace, the ones that connect my friend and me, heart to
heart. Two mortal beings, facing the
same ultimate fear of dying.
Happy Thanksgiving!
Jenna