Sister Cheryl reports a new state of affairs.
It was pretty cool to visit with her tonight, and get a totally different picture than what I gathered this morning when I popped in to see Dad on my way to a work commitment. And different than Mom's full update for me over the weekend. Finding out what's happening one mile north of my house from a sister who lives 1,724 miles away is just....well cool.
Sometimes I think the way Dad's days have been unfolding of late must be even more surreal for Cheryl and Jonathan and Daniel. They love him just the same, but get just bits and pieces, here and there, snippets, that must create a sense of disbelief.
So let me update you with the weekend's turn of events from Cheryl's side of the hospital bed. It's a bit more consise, and equally amazing.
CHERYL HERE . . .
(ok, it's Karen semi-quoting Cheryl)
FRIDAY NIGHT, 11 PM I speak with mom and Karen, who with Tim have been in Dad's room for the last 3 hours. Two of these, he spent in a complete comatose state...
Tim and Karen come by to say goodnight around 8:00 pm. After a blurry-eyed few moments, Dad closes his eyes and then becomes completely unresponsive. Mom is alerted and she drives to meet them. Together they watch as dad's status continues, unchanged. Other than breathing, his body does not move or shift in the slightest, and they are unable to awaken him or create any kind of a neurological response, even with loud voices and painful stimuli. (Thanks to dad's week in the ICU, we all know how to simulate the basic bedside neurology exam. For example, we learned the best way to elicit a response is to press hard into the base of the nailbed with a nearly sharp object, like the back of a pair of surgical scissors. So "pain" is a relative term in the neurology world.) Anyway, his status is at the very bottom of a coma scale, with no observable medical changes other than a fever. Then, after two hours, his status improves slightly...he is now spontaneously opening his eyes, makes a partial attempt to look toward their voices when they speak, and his body begins to move voluntarily again (but not in response to commands). They are calling to let me know that it appears his brain is "storming" again, and that this weekend might be the days that dad wraps up life. We all are "on call" for any further declines.
MONDAY AFTERNOON: I check in with Mom, and she is spending the afternoon with Dad. Mom hands the phone to Dad, and with his voice at FULL VOLUME, he formulates short sentences and tells me the things on his mind. His voice is slurry, but animated; his thoughts are complete but very random. All of a sudden, I have this recollection of a phone call I had with him when he was in rehab back in May: where he was disoriented, with confused thoughts, but was fully intelligible. In both instances, it's not really possible to talk him through his confusion.
WOW. Friday, he appears to be at a near "brain death" level again...just like he was when his massive brain storm hit on July 16th. But then on Monday, he is carrying on a full conversation...just like he was after his brain injury from his fall on May 15th. This is after weeks of not being able to hear anything but chance single whispered words, or see nods to yes/no questions. HOW WONDERFUL to hear his voice, after all this time! And how very unexpected.
And yet, within these massive changes, it appears his overall thought processes are unchanged; he is still very confused and concerned about things that he can't make sense of. It is difficult to console him or help him walk though simple information using rational lines of thought. All these weeks, it has been difficult not to know what is going though his mind. Well, now that he has voice projection, we know. And this is difficult too.
There's two ways to look at it, I guess: first, heartwrenching, and worse, to see his confusion out in the open and unchangeable. Second, still heartwrenching, but better, to know the truth about what is on his mind. For me, I guess if I could choose for dad, I would choose the second option. I feel some consolation that he, for the time at least, is able to voice his concerns. I imagine that this must help him cope with his confusion, to be able to verbalize his concerns, and feel the love of others in response.
BACK TO KAREN:
NOTHING IS QUITE SO AWFUL WHEN YOU GET TO TELL THE PEOPLE YOU LOVE
NOTHING IS QUITE SO AWFUL WHEN YOU GET TO TELL THE PEOPLE YOU LOVE
That's a theory I ascribe to, now more than ever. The outpouring of concern from long-time friends, both near and far...from my childhood friend Tammy and Tim's dear friends Doug and Deb (33 years but who's counting?), to OT classmates of 16 years ago, Kristin and Michele, and longtime Arcadia family Rachael, Erica, Patty, Emily, and Ulisses, to Cheryl's lifelong dear friends Sherrie and Tracy...to family who continues to keep the memory of Dad's full life in their hearts...
You are all so encouraging to us! THANK YOU for sharing in our days, our updates, this blog. Knowing we do not have to absorb dad's story alone is truly a gift that gives to us more than you could ever imagine.
Thank you for this update. I will give your mom a call this week. LOVE YOU, Gail
ReplyDeleteFROM A LONG-TIME ARCADIAN SPEECH THERAPIST, via FACEBOOK:
ReplyDeleteThinking of you, Tim and your family. This journey has to be so difficult, I just don't even want to let myself "go there." The blog is such a wonderful way to keep close with all the people involved with your dad. Take care. xxoo Patty
_____________________________________________
FROM ME TO HER:
thanks for the warm thoughts, patty! i remember you taking the time to get to know him one day in the office and helping us understand some of his speech needs. amazing to go through the hospice process as a therapist daughter. feel like it's adding so much to my repertoire of experiences that will help me in my therapy world as well as my personal life. thanks for following along in the blog.
hope all is well for you and your family!
xox k.