One year ago, Vernon was moved to Newport Subacute. There had been many attempts to get him into more desirable facilities, but in the end, this is what he got. As Justine learned in Preschool: “You get what you get, and you don’t throw a fit!” I didn’t throw a fit, but I spent the next three months trying to find a better place for him on my own. I still believe it was there that he lost his chance to one day walk. His right knee is permanently bent and both achilles are calcified. But now these things are the least of his problems. We did manage to find a new home for him at Mesa Verde, which we are very happy with…even though he used up his physical therapy benefits by summertime. If it weren’t for Mesa Verde, we would never have met Joe, a king among men, worth more than a thousand working limbs.
It was a year ago, then, that Vernon began outpatient dialysis at Davita, another place I have struggled to work with. We were only going three days a week then, and Vernon was still safe in his chair and didn’t need sitters. The facility is big on seasonal decorations, and I recognize the autumn leaf motif returning to their walls and ceilings a year later.
Though I’m recalling the past, I’m not here to complain. In fact, this reflection brings to light something positive for me. A year ago, I didn’t know enough to say “NO” to anything. I had my preferences, but I felt like we just got pulled into the tide of medical decision-making that often had little to do with our best interest. This still happens, of course, and I have gotten used to hearing “NO” over and over as we ask for more things that I think might help Vernon’s recovery or comfort. That’s the “system” we have in in this country. If you aren’t filthy rich, it takes a lot of creativity and stamina to get what you want in health care.
But something new happened this week: I was the one saying “NO.” It was a simple interaction, but it felt as if I had turned some sort of personal corner. I have to power to say “NO” even in the medical world.
I got a call on Saturday from Fountain Valley Medical Center, informing me that on Monday (yesterday), Vernon would be having a surgery on his left arm to fix the fistula that had been embedded in April. April! How can this be an emergency then? Basically the doctors at the dialysis center talk to each other but not to Vernon’s overseeing doctor or anyone at the Care Home. So even though Vernon has had to have two emergency surgeries in the past month, and though it took him almost a week to recover from the anesthesia from the most recent one (which was very scary), they were happy to put him under yet again to suit their calendar.
I interrupted the woman who was asking me the pre-op questions over the phone. “Can I put this on hold and get back to you after I call my doctor?”
I called Dan. “Is it life-threatening if Vernon doesn’t have this procedure right now?” He hadn’t heard anything about it, but he assured me it wasn’t.
“I just don’t think he can handle another bout of anesthesia so soon. I can’t handle it. We finally got him back for a few days after a scary drop in consciousness. I say “NO, not yet.” Can I do that?”
Dan assured me that I could. And he agreed that this would likely be hard on Vernon’s body and mind, so soon after the other surgeries.
I cancelled the appointment. And I have yet to hear anything from anyone in the nephrology/vascular/dialysis camps. So I guess it wasn’t an emergency, after all.
I do feel angry about this, how that camp sees him as some sort of machine to fix and tweak, not ever looking at the bigger picture. But I won’t throw a fit. I can just say “NO.”
I like the feel of that. It’s our turn to use the word…Lord knows I’ve heard it enough in this journey.
(That said, whenever I do our own thing…I have a niggling fear that I’m killing him. But at least we’ve got him in a good space for the time being. We can book it after Thanksgiving, instead.
On that note, I booked a wheelchair van for Thanksgiving Day. I had originally thought we’d aim for Christmas, but the last year has taught me that you must take advantage of the windows while you have the chance. If all goes well, he and Joe will be home with us for a few hours on Thursday, the 26th.
How is that for a big fat “YES?” It’s about time.
(Vernon, a few years ago. Just found this picture hiding in the archives. Who needs legs or kidneys when you’ve got a face like that?)
57
oh gosh i have to keep reading the date .. thursday 26th … holding my breathe .. amazing plan Allison..that will be just amazing … you can say yes or no ..but could we all skype that day??? ..make it a real thanksgiving family day..across the miles???
xx love to you all xx
stay on board! skyping would be great! I don’t know yet how he will handle things so it may have to be short. This may be sensory overload for him. We’ll play it by ear, but I sure hope skyping works out too.
ofcause Allison ..even if it is just a quick hello and a wave to you all… best play it by ear …what ever you think is best for Vern ….. fingers crossed we can sort out the skype!!!
Planning His Escape!!!! (for a while anyway)
Hoping it turns out you can do Thanksgiving and
Christmas at home this year!!!!
Tight Hug
Barbara
EFF YEAH. Powerful post.
Allison,
You have every right to pitch a fit but I guess it is better to just say “NO” and not let the drs. mess Vernon anymore than is necessary. I stand beside you in your decisions. God be with you and help you over every struggle and praise. And we do have a lot to be thankful for. So remind Vern and the rest of your family to be thankful for all we have at this time of year.
Hugs,
Becky Jones
Hi Allison,
I found your blog somehow when looking at Nicole’s FB profile. She and I have a close mutual friend. I’ve since read all the old posts and always look forward to your new ones. My nearly 7 year old is half-way through a 3 year treatment protocol for leukemia, so there are some small parallels in our stories. Something I’ve been wondering about, that I don’t know if you’ve ever mentioned in your posts … is Vernon expected to be a candidate for kidney transplant, or is dialysis the long-term solution?
*just corrected my blog address in my comment profile 🙂 *
HI! So nice to meet you here. I am so sorry to hear about that long plight with leukemia. And to have your little girl going through it must be incredibly hard on the heart. But also heart-building, I expect. We haven’t really looked into kidney transplantation yet as it seemed so far down the road with all his other problems, but actually even yesterday, his roommate brought it up, offering to give his own kidney if they were a match. I don’t know…maybe we are at a place we can start asking more serious questions about it. Seems too good to be true.