Are we there yet?

 It's your bi-annual update. The minutes of Dom's recovery for investor's of a heart kind.

The 7th anniversary of Dominic's transplant, considered a re-birthday in transplant circles, came and went on Thanksgiving day this year. How apt.

I anticipated the day, and then it completely slipped my mind as I ate copious amounts of delicious food. On the day of thanks, one of the things I am most thankful for slipped my mind. I blame the pumpkin pie cheesecake. Not the tryptophan as I do not eat turkey.

One thing that weighed on me as the day approached is how grateful I am not just for Dom's extended life, but for all the love that was showered on us, and all the practical gifts of financial aid and the handful of people who made food for us. I found myself randomly composing thank you notes in my head these past few weeks. It's been over seven years now, but the impact lasts a lifetime.

This year hit a little different. We lost Dominic's mum in October, which is also the month we lost his sister in law Alison, just two years before. Dom did not have the energy to make a trip overseas for her service. That reality was something we'd talked through long before we lost her. We are grateful for the wonders of modern technology which allowed him to have conversations with his brother in the UK and sister in Qatar at the same time. It was so lovely hearing everyone, including Sam's husband Phil and Nick's daughter Hannah chatting and sharing stories about Ma and about moving forward.

So, it's not really that the anniversary slipped my mind; it's really that the days have been flying by. I always stop looking at numeric calendar days around Thanksgiving, just knowing, I have to be ready for a feast by the fourth Thursday of the month. And we were very ready this year.

My little reports in June are always full of so much anxiety for the fire season ahead, and come November, (now December), we've had rain, the brown fields have turned green, and the venomous snakes have mostly gone into hibernation. We celebrate giving thanks and fill the house with twinkly lights. It's my favorite time of year. It always goes by too fast. I try so hard to just sit in the season, and let it all soak in.

We're still in the June of Dom's recovery. Every 3 weeks, we go for his treatment and tests, and adjustments are made and there's talk of more frequent treatments and different therapies. I log onto his on line medical records and scan the test results. I live in anxiety that the protein count that indicates how his kidneys are functioning will have bolted again. There's been threats of putting him on a regime that would require weekly visits again, and I fret. I don't think I can do that again.

I'd find a way, if I had to.

But, we're ready for the post rainy season. We're ready for Dom's recovery to be that once a year visit Dr Carroll thought we'd transition to by now. We're well past that period. We're ready, but not there. 

So we continue to do what we can. Someone once said to me if her husband wouldn't do all the social things she loves to do, she didn't know if her marriage would last. What you do is, you adapt. You bend and flow. There's nothing I want to do without Dom at my side. We don't really feel like we're missing out, we're living to the fullest as we're able. And, I'm so grateful for the friends who have bent and adapted with us. It's such a tremendous thing to be so cared for.

And to be able to do it here, on the secluded property where we live, in beautiful Sonoma County, is a wonderful thing. 

We had a lovely visit with friends from Georgia in October. We have comfy outdoor furniture and amazing views and just enjoyed the time together. That visit was followed by my brother and his wife. We'd worked so hard to get the barn space ready for the first visit, it was a breeze by the next. (And our first visitors did a lot of the heavy lifting for me). Then Charlie, who owns our home, came for a visit and we had a gathering to celebrate his daughter's birthday and catch up. 

It's the most company we've had since Covid hit. With his compromised system, we're still very protective against viruses. We're generally open to visits on pleasant days, as we can sit outside and feel a bit safer.

Dominic is still extremely fatigued. He can do things throughout the day, but they're done slowly and with naps. I realized just today that I've had a weensy bit more energy. When we came home after the three month hospital visit, I was a mess. I needed daily naps as if I were the one getting treatment. But, the all night beeps and the worry and the driving were more than a full time job. It's nice to feel a little better. Dom feels a little better as well, but, the reality is, a little better is still not well.

We've made it through another "fire season". The last month of summer and first month of Autumn, we're on pins and needles. When the 2017 fire burned my Mom's house to the ground, it shocked me how little there was left. I've seen house fires here and there. Sometimes, you can't even tell there is damage, except some windows are boarded up, or there's a black singe on a wall. Sometimes, there's a big black hole, but the rest of the house looks pretty intact. I'd never seen the likes of what happened in 2017. What remained of her home was a pile of ash and a shower stall. On a bad day, that feels like what remains here as well. Maybe, if he'd only had Leukemia, he'd look like that house a little boarded up, but mostly intact. This gvhd has been a house fire that has been all consuming.

But Phoenix rise from ashes, not boarded up windows. 

So Dom is returning to himself little by little. He's been drawing every day. He made charcoal to sketch with. He questioned if it would be okay to have a fire after it rained a solid week with absolutely no let up. They call it a bomb cyclone these days. It results in an "atmospheric river" that means a lot of water is dropping in a short amount of time. I breathed a sigh of relief and proclaimed it certainly would be okay if he made a fire outside. I'm thinking a few more this season, just to mix it up. We can unplug from Netflix and bundle up with with the view. 

He's still shepherding the chickens from our ever present bobcats, coyotes, and sly foxes. We love our silly girls and love for them to find slugs and snails amongst the garden areas.

We got a hot tip from a friend that the Northern Lights would possibly make an appearance, so having missed them the first go round, we hopped in the car and made the journey about an hour north and we ticked something off the bucket list. It was such a treat to see them. Perhaps they weren't as dramatic as further north, but they were here and they were mine.

So, we're doing alright. We're on a journey we never thought we'd be on. We also never thought we'd see the Northern Lights all the way down here. But here we are. Taking things as they come and cherishing what is good.

PS: The wonky pool table is open for non-serious pool. 

And this kitty is open for scratches if he's not recovering from a big hunt.

 

 

Alexander moves to Australia (or Iceland)

 

 

Having always been enthralled with Alexander and the Terrible, Horrible, No Good, Very Bad Day, I like to laugh at the absurdity of bad days. Or weeks. Or years. Because, if you know the book, there's always Australia (or Iceland). 😉
*Please, only read this with a sense of humor* No sad faces please.
Wednesday was our 10th anniversary. Yes! 10 years. 7 of which have been dealing with disease, doctors, hospitalizations, and finally, the dreaded Covid. We're waiting for our prize.
We've been squirreled away. Limited contact with the outside world. We're a little feral.
We got very excited about a restaurant getting rave reviews for its gluten free pizza. Dom had just lamented ever having a good pizza again given his restrictions. Then I heard about this place. It has an expansive patio, and we thought we'd risk it for lunch. And if it was too risky, we'd have a picnic nearby. (Dom is still high rick for Covid and Measles as well.)
I packed our cooler with drinks to be prepared.
I pulled out a summer dress I'd bought at Christmas and had tucked away for warm days. I was so excited to have an occasion to wear not just a dress but the dress I'd pined for, for some time before nabbing it in an outrageous sale.
I slipped it over my head and noticed as it shimmied over my shoulders, a giant hole in the back.
A brand new dress kept in a protective bag. Damaged.
I'm a sensitive sort, and it was difficult to not feel a lot of it's not fair. Life is hard. Why me. Over a dress. But wait.
We hopped in the car, sun shining, smiling, anticipating our first date in 7 years. No really.
And then, the car died at a full stop. Huh. I must have stalled it. (Proud driver of a manual here.) Only. It happened again at the next stop. And again. And so, we turned home,
The next day we'd have to be in Sacramento for Dom's treatment. We didn't have time to take the car to a repair shop. Dom did a little research. Went with best case scenario. Fiddled with the oil dipstick, heard a pop, drove up and down the drive with no problem. We decided he'd fixed the problem. Anyone who thinks we're negative nellies does not know the amount of positive thinking we exert on the regular. But our denial/positive thinking got us to Glen Ellen before I ruefully turned the car back toward home.
Mom raced from her house 40 minutes away at the ready and we made it to the appointment just an hour and a half late. Because here's why we didn't cancel our appointment: Dom is their favorite. There was a training happening and they always juggle Dom in on those days because he is so easy going and has the best veins. It's a thing.
And here's why I don't want any sad faces. I got to spend time with my mom and in Ikea. We had cinnamon rolls. (Nicky's are a billion times better, but when in Rome.)
We were an hour and a half late, but only half an hour later than usual headed back home. Neat how time works.

 

We got home to no internet. Someone accidentally cut it. I had a bit of work to catch up on, but had to postpone. I was so frazzled by Friday. I got up early and fed the chickens. A task Dom is usually happy to do. I wandered down to the fish pond/tank after feeding, as it always makes my heart happy. (This is an old photo being enamored with the fish.) On this morning, it did not make my heart happy. The barn is being painted and having minor repairs. Woodpeckers have been tucking acorns in the roof. Someone scraped the acorns out only to fall into the pond. The tannins would leach out and kill the goldfish. I immediately began fishing out acorns and detritus, bailing out water and giving it a spring clean. And we laughed, because what else am I supposed to do without the internet?!
I was feeling real sorry for myself Wednesday, as we were supposed to be celebrating our anniversary.
But by Friday, having run back and forth between house and barn cleaning the tank, fixing the internet, (we currently have 100 feet of cable running across the drive connecting me to you), I didn't have the energy to feel much of anything but grateful for the tub of ice cream in the freezer and the husband I would still say yes to, even knowing what we'd be in for.
The dress is being exchanged.
We have the $ to repair the car. (Rats are chewing through wires. Ugh. Country living!)
We made it to the doctor.
The internet is (mostly) running.
I'll get more goldfish.
We'll get to that restaurant.
*Dom is still with me.*
The traditional 10 year anniversary gift is tin or aluminum symbolizing resiliency. Maybe I'll start calling Dom my tin man. Only, he does have a heart. And that my friends is what it's all about.

This photo was captioned: Sometimes when you're on your knees pulling weeds near sunset and you look up.
 

Liminal spaces in Haunted Mansions

 Dom and I have been in a liminal space for quite some time now.
Liminal is defined as occupying a position at, or both sides of, a boundary or threshold, by the Oxford dictionary.

Warning: this will be a rather esoteric or existential musing. I can’t promise anything here but my rambling thoughts.

Liminal spaces are sometimes described as hallways. It’s the transition from one space to the next, but it’s not the destination. It’s just the space you occupy to reach the next room or space. It’s also the emotional space before transitioning. ***But what if your hallway feels never-ending?

We just watched The Haunted Mansion. I loved the ride at Disneyland as a child. I was terrified of scary movies and scary things, but the Haunted Mansion is set in a New Orleans style square and just outside the line for the mansion upbeat New Orleans jazz plays. I loved the cheerful music, and the well tended shade garden as we wound our way outside the grand mansion to get inside to the ride. The depictions of early 1800’s gracious living over ruled my juvenile fears of haunted houses.
But I digress. I’m thinking of a particular aspect of the tour punctuated in the movie. One of the main characters is running down the hall trying to get out and the hall just keeps expanding so he can't get out and then and there I am feeling it. The hallways in the mansion were ever expanding to keep the characters from getting to where they were going. They were stuck in a liminal space, if you will. 

In the Disney attraction, even before you see the endless hallway, you enter an anteroom that is really a sort of stretching elevator. The portraits hanging on the wall begin as innocuous paintings of innocent looking people and stretch into something ominous, revealing something sinister behind the innocent facade, all while a ghost voice ushers you through. When you exit this room and make your way down a never-ending hallway, the portraits here look like lovely people or pleasant scenes and transform into something garish and freaky when lightening strikes. Everything is not what it seems. And it’s all just a passage. Technically, at Disneyland, you’re still “in line” for the “ride”, but you’re actually also inside the attraction and experiencing the event. You're both in a liminal space and in the destination.

Beautiful lady

Is actually balancing on a tightrope. Hmmm...feels familiar.

 

Feels a lot like where we are now. We’re still in the liminal space of waiting for the next step, but we’re also in life. It’s here and now.

So I have to wonder if we’re really trapped in this haunted hallway of transition that should have been just a quick jaunt from one room to the next, or if we are actually on the ride already, and I’m mistaken that we’re stuck in a hallway that won’t end.

 

All I know is: this entertaining and enjoyable movie brought up a lot of feels for me.

Before cancer was one place. After transplant was the next. We thought we would transition through hospital stays to the great “back to life” of living at home and being recovered and moving forward with our careers and lives.
Only. The debilitating Gvhd. It stretched our threshold of transitioning.
And then Covid. Without a doubt, this new world of a highly transmissible airborne virus has ushered us firmly into what feels like a never ending hallway of waiting complete with spooky paintings and ghostly voices.
I feel like we both thought if we can just get past this, we’ll be free to move forward, but the threshold keeps moving. It feels like we’re endlessly running and the door is just out of reach.

If you look closely at the image below, you'll see the transformation. Sometimes, the impact of Dom's disease and Covid makes me feel like the final portrait, but being home, with our beloved things reminds me that it's just a ride and it's full of laughs.

 

So don’t get me wrong. Can you tell I love Disney? I do. One thing I’ve been really bummed about these past six years is not being able to introduce Dominic to Disneyland and to invite myself along when my special Cece went for the first time. When I got out of high school, I got a job at Disneyland. My cousin and I would go spend time in the land themed New Orleans Square, enjoying the ambiance. To be able to see myself in a Disney story should feel a little comforting. It's such a familiar place. It has brought me so many good memories. Only, I didn’t realize of all the Princess and Fantasy options, I’d relate to the Haunted Mansion. (To be honest though, I’ve also fallen down the Rabbit Hole and met Caterpillars and Mad Hatters.)

All that to say; it’s not bad to be in a liminal space. And I don’t feel horrible that life didn’t turn out as we planned. I do feel a bit under equipped. There’s “What to Expect When You’re Expecting.” You get a guidance counselor in college. I grew up in a church where potential life partners received marriage counseling before tying the knot. But, no one plans on cancer. Or disability. It just happens. We had just exited a liminal space before the cancer. We had just, finally, at advanced ages established ourselves into our career goals. We had exited the hallway and were in really grand rooms with people and prospects. I finally felt like a certified grown up. I've been regressing ever since.

The funny thing is, the Facebook algorithm lords noted my search of liminal and suggested for me an article in Architecture and Design. Seriously. All my chat about hallways and art and liminal spaces led me to a design magazine. So, I clicked on the article and came across words like nostalgia and kidcore and I’m shaking my head yah, yah, I get it. I am totally feeling this. I just bought an ornament that depicts a nursery rhyme reminding me of the children’s cutlery I used as a babe. Also, I bought a dollhouse to paint. I am totally feeling nostalgia and kidcore. I’ve embraced whimsey as my primary decor aesthetic. Embracing this has brought me a lot of joy. I am digging this article that seems to affirm my regression.

And then I got to the last paragraph. Mind you, this is after I’ve decided that Dom and I are currently stuck in a liminal space, and I'm actually embracing the life we're building in our hobbit hole.
But the critical thing is—though you are nostalgically drawn to these spaces, you cannot overstay your welcome. Spend a few minutes embracing this amniotic bliss—in the end you have to leave.

And now I feel like someone yanked me off my unicorn.

I have no idea how we’re going to outrun this hallway.
Dominic and I definitely move differently. We’re processing all that we’ve been through differently because we’ve experienced it differently. But we’re both experiencing the alienation of isolation. We’re grappling with what it means. And, we’re grappling with what the room will look like when we get out of the hallway.
We went out with friends recently for the first time since Covid happened. 3 years, and it was our first, and last outing. We met outside at a cafe for coffee. As we’re telling these lovely friends that it’s been so long since we’ve been in a social situation like this, we felt like babes in the woods, something funny happened. We’d ordered pastries and the cashier brought them out to us in little paper bags. We all reached in and started taking bites. Dom pulled his pastry out and put it in his mouth. A peculiar look crossed his face and he blurted out “babe” in that special way that holds so much meaning between couples. I looked at him fearful of what he’d discovered. Was it a hair? A bug? What caused this plaintive cry? His pastry was in plastic wrap. I still can’t even tell this story without laughing as I type because it is so nothing and everything at the same time. I fell into uncontrollable laughter. This man, who is still most definitely a man, who has endured so much and also relied on me for so much could only cry out to me when his pastry was in plastic wrap and it just stunned him into crying out to me for some explanation. We both laughed into hysterics at the absurdity of it all. And our friends looked at us a little bit like they may need to back away slowly.

And that is a lot how we feel in general. Nearly everyone has backed away slowly as we’ve devolved into hobbit like creatures who just want the comfort of home and a nice warm cup of tea.
And, we’re not entirely sad about it.
The world has gone mad. Well and truly bonkers. It feels a bit more “off with their heads” mad than Mad Hatter. (By the way, a friend just wrote a book of recipes inspired by Alice in Wonderland, and I will be having Alice inspired teas and parties outside. You should come.) 

But, as you can probably tell from my many allusions to the never-ending hallway, not much has changed here.
And in some ways, in a lot of ways, that’s okay.

Post script:

 The book is called Alice in Wonderland The Official Cookbook, published by Insight Editions

Just for funsies, my brother went to Disney's Haunted Mansion to capture some video for me. I'm not able to insert the videos, but here's a few more stills and his youtube channel. Hearing him laugh through the ride made me laugh out loud. It was good.

Livinlifeanimated

 

 

Old tricks, new tricks

 This morning, my social media memory carried me back to the hopefulness of five years ago. The belief that after the stem cells of a generous donor were safely deposited in Dom's body, we'd soon be able to get back to our old tricks.

On the bright side, the cells are safely in his body.

This blog has become somewhat of a bi-annual observation these days. How do I write "we're still plugging along" over and over? But we are. We may not have the exciting twists and turns of will there be a donor match? Will the transplant take? Will the people upstairs in our temporary apartment ever stop partying with shoes made of clay?

Just like a daily dose of nature is as good for the soul as a once in a lifetime trip to a natural wonder; it's the daily gratefulness and observations that keep us going. It's good for my soul to take stock and look forward while looking backward. It occurs to me as I write this that I wouldn't make a good Buddhist. "Here now" is the culmination of all we've been through and what we hope for. I'm not interested in emptying my mind. I am interested in meeting the day with the knowledge that our hopes are very simple. To live while living.

So, how are we living? Much the same as the last few years.

We set our alarms to make the trek to Sacramento every other week. It's really quite a thing that now that we're "old" people, we wake early naturally in the morning, (sometimes really early since Dom is on steroids.) But Sacramento mornings, my alarm goes off and all of a sudden, I can fall into that elusive deep sleep I've been longing for. But I can't because we've got to go.

He's been on steroids for far too long. Most stem cell transplant patients are completely weaned off  immune suppressing drugs by now. Our Dom is special. You know how your immune system kicks into gear when you have a cold and it wipes out all the intruding bacteria/virus and you're back to normal before you know it? Well. Dom's immune system continues to see his vital organs as intruders and sets about wiping them out cell by cell and won't stop until his organs are wiped out like a cold or flu. He continues the UV therapy. The nurses continue to marvel at what beautiful veins he has. The doctor has concerns. Here we are.

Our journey has taken us from a bustling hospital unit with dozens of nurses we got to know; I was actually in some ways excited for his 5 day hospital stays so I would actually get to visit with people. From there we spent years visiting the Infusion Center where again, we would see dozens of familiar nurses and while many people were seriously ill and there was an air of somberness, there was also an air of celebration and camaraderie for each small step. The Infusion "Center" was actually 3 different locations. Two of them were bustling. As time wore on, and Dom's treatment transitioned, we were sent to the smallest center, and the specialized machines used for Dom were in the back corner away from the hustle and bustle. At times, the quiet is nice. But it's not the same as when we'd walk into the bustling center and it was like an episode of Cheers, only they'd be calling out "Dom" instead of Norm. I even miss the beeps and alarms that kept us awake all night in the hospital and followed us through each center.

And now, the hospital and doctors have been rearranging and consolidating and we are in a closet on the ground floor tucked in behind registration and see only our nurse and maybe one other. 

And it feels very much like our journey.

In the beginning, people were riveted by our story. We were surrounded by caregivers and concerned friends. As time has worn on, things continue to shift, and downgrade, and sometimes, it feels like our life has been distilled down to the people I can count on one hand attending to us in our closet.

Life imitates art, and apparently can also imitate medical organizations.

Five and a half years into the diagnosis and two and a half into a pandemic, I finally got a sourdough start. My first loaf was almost perfect. The following two were heavy. I'll leave that there.

Dom's full time job continues to be living. Being on steroids is no fun. Our marriage is a good one and we've made it through a lot of things others would crumple in. But steroids? Hoo boy. I'm going to want a gold star when he's finally weaned off of those. We've had a few moments where we just stop, blurt out "it's the steroids" and move on. He has good days and bad days. He has days where he can putter around outside and days he is one with the couch.

There is no prognosis at this juncture. The body will do what it will do and the doctor studies his numbers closely. There's talk of seeing a kidney specialist next because they are taking quite a beating. Dom is eager to be productive, and he does what he can. 

We're trying to imagine what life looks like given our situation. We both have to reinvent ourselves, but in between the reinvention is the reality. I need a better job to support us both, but the pandemic threw a secondary wrench into that. 

And in spite of all that, we are laughing and loving and being. 

Throughout his illness, we've been stunned by the precariousness of life as well as how capricious death seems. It felt so weird that Dom's life was hanging by a thread and we'd hear news of a police officer shot in the line of duty or a firefighter down in a fire and we'd talk about the lack of rhyme or reason. We experienced that in an even more intimate way this year, as his brother's precious wife was taken suddenly and unexpectedly. She was just two months older than me, very active and just like that, we lost her. I cannot make sense of all the times she supported us throughout Dom's illness only to be the one who is snatched away from us. She was a beautiful human being and dearly missed.

We continue to take so much joy in our animals. Out of seven baby chicks, we did not get one rooster! For months, I studied their markings and behavior and was convinced with my luck, we'd have seven roosters. If you haven't just stopped and watched a chicken run recently, I highly recommend doing this. Just like so many things on my mind today, it defies reason.

 

The bobcats still approach the cage as if it's a vending machine. With the help of friends, we've enclosed the whole structure. But we continue to be vigilant for hungry predators. Yesterday morning, a fox came by. 

We're in love with our stray cat. Houdini, unlike his predecessors, is not a lap cat, so when he does come around with purring and nudging, we're thrilled. I always did love the hard to get creatures. He melts our hearts every day. We're especially grateful for him as we lost one of the other boys. Our Errol Flynn is gone now. The cat I was so desperate to get home to all that time in Sacramento, the wily cat who made my neighbor cry when he escaped the carrier during the fire that nearly burned our house and she was trying to rescue him, the one who made peace with Houdini and ate side by side with the new kid in town. I do not deal with loss well at all. It is an inevitability. These years have been a Master Class in acceptance and growth. 

It was Dom's first try at gardening this year. I think he's hooked. It's a battle against the critters, but we try. The bare root apple trees produced four apples this year, and we call that a win. He developed an appreciation for Kale and the chickens feasted on tomatoes.

 

I've been sitting on this all day. It just reads like a Christmas card, but really, I have so many things I want to share. But not like an apple pie I can cut into pieces and just give you a piece, more like an apple cart someone can push while I pull. 

I have a lot of thoughts around the words blessed and grateful. Dominic and I have never asked "why me?" through this whole ordeal. But why not me? Is that an equally unfruitful question? 

We are so grateful. But life is also nuanced and blatant and complicated and simple. I'm not sure where I can write all the other things that are just as real and true as we are grateful. I think this sums up what I'm trying to communicate perfectly.

 

Another year, another animal

It's been five years now. I'm so glad I have this on line journal to look back on. Even if I only write once or twice a year, it's perspective. Looking back on last year's sharing, it was very heavy. 

Thanks to this little guy, this year feels a lot lighter.

We'll be celebrating the one year anniversary of his unexpected arrival in a couple weeks. He showed up one night hungry and scruffy. I looked for his owners. I looked for a new home for him. Lots of people said he was meant to be mine, but financially, even just a cat is a frivolity. But, potential owners didn't work out, (I made a new friend though!), and I just could not bring myself to give him up to a place where he'd be in a cage or a small room until adopted. He'd been living on his own outside and that just seemed cruel.

So, Houdini the little escape artist became a part of our family. I'd shared about him on social media. The first night we noticed him, he was so hungry, and I'd later discover injured. It was dusk and he scampered by me as I was walking up the trail and sat down a few feet away. He just sat there lifting his head to smell the breeze. He seemed completely unbothered by his hunger or his wound. He just enjoyed the night air. He made his way down to the barn and stayed the night there. He lived in the barn for a while and it took a bit of maneuvering to make the barn secure. He was so independent, he would push his way through the doors we'd barricaded to keep him safe at night and dig his way out. He wanted out. And he wanted in. I can really relate to that. We want what we want. 

My working class Brit teased about him getting his boots planted firmly under the table. This is true. He charmed his way right into our hearts. Over time, his wound healed and his coat became soft and glossy. And he makes us laugh and smile all the time. He's bright, friendly, and curious; he wants to know everyone. I guess, in some ways, he reminds me of Dom. Life has been pretty precarious for Dom, but he'll still walk outside, lift his head into the breeze, and just take it all in. He too is healing from his wounds, and he's been taken in by all of you. You've fed him and cared for him. You've made it possible to get treatment he needs and continue to cheer him on as he faces the lifelong disease of gvhd. 

Sometimes, we're hanging on by a thread.

But we are hanging on.

Last year, I was so exhausted. I had actually found myself crying uncontrollably the entire month of June. I felt alone and in some pretty deep despair.

July was a game changer. I shared here that Dominic was able to be fitted for contacts that protect his eyes. He was going blind and in constant pain. We had to get them, and if you remember, a group of artists had decided to give him the remainder of some funds they had which amounted to almost the exact amount necessary for the contacts. We still live on that divine grace.

The pandemic shifted things for us and for me. It made it easier to let go of some things. It is the strangest thing to be on the cusp of normalcy only to have the whole world shut down and then try to find a new normal and actually there is no such thing. I realized, what we all crave is not normalcy, but comfort and adventure. 

Our adventures remain our trips to Sacramento. We go every 2-3 weeks for Dom's treatment. He's kind of at a stand still where we still hope for forward progress. He's still on large doses of anti rejection medication, which should have been over by now. He continues to suffer a laundry list of ailments that we treat like whack a mole. Oh that some wet cat food and a safe home could cure him. We balance hope for progress with cheerful resignation. He is alive. He is able to help where he can. We have Houdini. All is well.

Thanks to the contacts, Dom is also able to drive a little. It was not a possibility last year at this time. We make a stop on the way home from Sacramento to pick up paperwork for my job and he drives the final leg home. It's been so good for him to be behind the wheel and taking back more of his autonomy. He's also been on the tractor as we have acres of fields to mow. This year, he's been able to help me more. This is good for both of us! We spend lots of time outside. This is one of the gifts of Covid, I think. Since we knew we'd be spending a lot of time at home, we've done what we can to make it a happy place. We don't own our home or the property, so everything we do is mindful of that detail. We're also mindful of fire danger. But, in between all that, we've planted a garden again this year and to plant a garden is to hope! We did a re-haul of the chicken coop, hopefully protecting them from bobcats and foxes, and started a new flock. (Thanks to my anonymous helper and Charlie G and Bob for their help on the coop.) And just to add to the poultry farm, we have a resident Tom. We call him Turkey Lurkey, and since I started feeding him leftover grains, he's not going anywhere. He has a damaged leg and limps around grazing on the last bit of field we've left untouched for him. We eagerly look for him in the mornings.

These things all give us life. Just being and helping in small ways where we can and breathing in the air.

No one can ever convey the intricacies of their life to another. My own mother who I speak with every day is continuing to learn and understand how we are situated, so I realize our own odyssey can be difficult to wrap one's mind around. Life as we knew it has changed irrevocably. Our goals and dreams have changed. But the one thing that remains is love. I shared a book page of the The Boy, the mole, the fox and the Horse by Charlie Mackesy yesterday, I'll leave you with it:

"We don't know about tomorrow," said the horse, "all we need to know is that we love each other."

 

 

 

 
 

 It's been 4 years!

I opened the blog, and it's been so long since I've been able to write, the interface is different! I opened the blog to my last unpublished post exclaiming now I can write. Apparently, I could not.

I've thought of y'all these quiet months of recovery and a worldwide pandemic. I've wondered how you're doing with the changes and the ebbs and flows.

It's difficult to believe that just 4 years ago, we were advancing in careers we'd both trained tirelessly for, the fires hadn't hit our hometown with a vengeance and become all consuming, and we were wondering if we'd one day have children, even if through fostering.

I had to stop writing because our story just didn't seem fancy anymore, this thing we're experiencing. I felt like a broken record. The grief was beginning to well up in me and any flowery or funny thing I could say was being usurped by this is hard. This is unspeakably hard. But dangit, if Dom and I are not the Energizer Bunny, I don't know anything anymore.

We have now been a couple in sickness longer than in health as we celebrated our seven year anniversary. And I want to tell you the raw bits, but I'm afraid you'll run away, because it's no longer entertaining. The numbers have all merged together and we've stopped the trail of one to pick up another and I've lost many of you on the trail; many of you are still on White Count and we're on alkaloids and proteins. 

So do I share the nice first, or the raw bits? I could tell you that right after I typed this sentence a coyote started barking in the field. I thought it was the neighbor's dogs until I really looked out the window. The dogs wander alone, and we've inherited chickens, so I needed to make this canine most unwelcome. Is my grief a canine? Seems so funny I'm typing away about rawness and am visited by a barking coyote.

When we got the news that Dom had Leukemia, I charted a course. He'd have one month in the hospital and then we'd be on the road to recovery. Then the news came that he had the kind of cancer that would need many rounds of chemo. So I charted that course. I knew lots of people who did their rounds of chemo and then there's a light at the end of the tunnel. Then I found out that between rounds of chemo, there would be infusions and many 4 hours round trips between rounds of chemo. So I lost it a little bit, I mean charted a course. Then I found out he'd need a bone marrow transplant. And we'd have to move to Sacramento for a few months. So I charted a course. Everything was new and shiny and we were held up and supported by so many people. I was surrounded by medical staff. People brought me coffee and sandwiches. My rig was equipped.

Somewhere between the bone marrow transplant and today, I'm not sure where, I lost my mojo. I'm not sure if it was him wasting away in the hospital having one of the worst and deadliest cases of gvhd or the insurance snafu that required a minimum of thirty frustrating hours on the phone between Christmas and my birthday in March of 2020. Maybe it was the long recovery that is not going as planned. Or perhaps it was the pandemic right on the heels of pneumonia. Needless to say, I feel like the Christmas paper crumpled and shoved in a trash bag. My usefulness served, and now I'm creased and tape has ripped away the ink. The paper is in the bag for a reason, and sometimes I feel that's where my words belong too.

I was feeling incredibly lonely. People I reached out to and was so looking forward to seeing flaked on me with an apology which rang so hollow after all I'd been through. Dom was losing his mojo too. I think it's a miracle he got to attend his sister's wedding. He had just under a year to build strength to walk and put some weight back on his emaciated frame. While in some ways it was a triumph to get him back home to be with his family, in other ways it bled me dry. I was so afraid he'd get sick while overseas. Your pandemic fears were/are my every day fears.

Upon our return, it was clear he'd turned another bad corner. So here's the nitty gritty. He has one of the worst cases of gvhd. (Graft vs host disease.) The new immune system continues to see Dom's own body as enemy cells that need to be eradicated. He struggles to breath as his lungs are attacked. He struggles to keep his eyes open and moist. He can't feel it, but his kidneys are being attacked. You guys. We had one week. One week between his liver being the thing we were keeping an eye on to his kidneys being the thing. He's been on the immune suppressant that most BMT patients are weaned off of in the first year in addition to massive steroids. This is not sustainable. I am not sure how to chart this course. We go every week, the four hour round trip to receive a treatment that takes 3 hours. Sometimes more. We go to a local eye doctor twice a month where he has had plugs placed in his tear ducts and more. The treatment for his eyes may yet be out of reach. Sometimes he also needs an infusion to boost his immune system which takes another 3 hours. He is a human pin cushion. He gets a needle in both arms, sometimes his hand. One needle is so large, he must keep that arm still. Blood is taken out, the white cells are spun out, zapped with UV light, and sent back into his body. No one can explain how this works, but somehow, it does? Some mornings, as my alarm goes off at 5, I question its efficacy.

But we jump through the hoops.

Two of the group of five who had transplants the same week have lost their fight against the cancer. We've lost track of the others. The doctor has confidence that with his immune system being such a fighter, the cancer will not come back. The silver lining in this is Dominic is still here.

Dom is in much better spirits than I am. He's so grateful to be alive. We're both so grateful for the support we received. We'd never have made it without so much generosity. Some of you really were the difference between eating or not. That's to say, we haven't gone hungry and we have a roof over our heads. Life is good. And more than Dom, I sometimes struggle to see that. I realized sometime after his lungs started failing that we would never go back to normal. While people have been clamoring to open up during this pandemic and fighting because they were asked to wear a mask, I've been processing how to move forward as both caretaker and bread winner. (I am not a bread winner. I could not even make a single sourdough this whole pandemic. This is not me.)

Dom is having to find himself again. He wants to work, but it's not in the cards right now. Especially with the pandemic. The vaccines did not pose a risk for Dom, but in all likelihood, his medication prevented the efficacy of the vaccine. So, we continue to live with great caution. We're so fortunate to live where we do. It's beautiful. It's secluded. And, it's allowed Dom to putter in a way that allows him to rest when he needs to. He built some fairy houses, and if anyone local needs a fairy house, let him know. We've convinced our Cece that fairies came in the night and built houses here and there. We sent the fairies to her house as well. Only the fairies can open the doors and windows we tell her. We believe in Santa round these parts. Life is too harsh to not weave stories of whimsy from time to time.

 

He rebuilt a rock wall at the entrance to the property. It's all just slow and steady. Friends loaned him an electric bike which allows him to test his strength and get around when his lungs can't get him the breath he needs to get up the hills here. There's much to do here always. Trees to cut back, weeds to mow, walls to paint. He said it's like the Golden Gate Bridge. Once you get to the end, you have to go back to the beginning. It's never done. I sometimes get overwhelmed but he keeps plugging along. 

So that's where we are! While others perfected the art of baking sourdough, or scrambled for childcare in this last year, we've just hammered on. We've been stunned as people who have offered encouragement have themselves succumbed to the frailty of life. I hesitate to share too much. (Was this too much?), but am happy to share more details of my own spiritual journey privately. I dreamed of one day having a party with all those who have been so supportive of us in this journey. Now, I just dream that you all know how very special you are to us, and how grateful we are to know you and that you are well and content.

 

All the best people are:

Dom's new birthday is in one day! I should be writing a celebratory post about the fact that he has lived a whole year as a miracle. And I will?

But for now, I feel like speaking to the care-taker of a blood cancer/ bone marrow transplant patient.

Let's climb into the Wayback machine to returning home after the initial diagnosis and two and a half weeks in the hospital, which felt like too long, but would in fact be only a drop in the bucket.

There is this thing called neutropenic which is a state that anyone undergoing a white blood cell killing chemo will be in. It means they have no immune system. It means you dear Caretaker may be out of your mind wishing you could get your hands on a giant bubble like the one John Travolta lived in in the movie Bubble Boy.

It means you will go through all your knives in one day because once the butter knife touches the bread, if you need more butter, you'll have to get a new knife because crumbs can't contaminate the butter because mold may grow? I was out of my mind friends. Now I just let the cats lick the butter knives clean before I go back for more.

I'm not going to say relax Caretaker. But relax. It could be a long road and you'll need to pace yourself and your butter knives.

I bought stacks of towels to pat things dry with and immediately put in the laundry before they become mold infested colonies.
Hey. That's not a bad idea. Have you seen studies on towels? Ew.

You yourself may undergo some bodily changes Caretaker. That's okay. You may be faced with a dilemma of not wanting to eat because you're so upset, but then you almost faint because you're actually quite hungry and once you start eating, you can't stop. That's okay. If your partner finds they can't eat because of chemo or the dramatic changes in their body post transplant, you'll wish you could actually eat for two like a pregnant woman because, well, you are eating for two. That's okay Caretaker.

And while we're on the subject of moms and babies, you're going to be tired. So tired. Like you've never known. Or maybe you have, who am I to say? But take naps if you can. Take naps if you can't. Sleep is a friend like no other.

Speaking of friends, sometimes, you'll feel isolated. It will be lonely. If you, Caretaker, are married to the person you are care-taking, at times, you may feel like you've lost them. What is important is that you do not lose you. They are still there, they just may have to do a caterpillar thing for a while, but they will emerge. You must take care of you. You are emerging into something new too.

You'll feel isolated because it's a tightrope you'll walk between letting people know you have to exercise extreme caution to not get the patient sick, but also that you are dying inside looking at the same four walls and you neeeeeeed a friend to reach out and risk everything just to make you smile. You need someone to sacrifice a little bit to meet you where you are. I'm hanging from that tightrope myself friend, so I'm not sure how to advise you on this. But just know precious Caretaker, that some friends will absolutely amaze you in the way they show up. Focus on that.

You will get a lot of advice Caretaker. A lot of advice. Advice is the currency of help oftentimes. It is almost always well meaning, and so here is how you take it: take it as love in your bank. I urge you Caretaker, to not actually follow all the advice given. Lots of people read lots of information and sometimes the sources are dubious and sometimes anecdotal and sometimes it may sound good to just drink fruit smoothies to fight the cancer instead of undergoing gut wrenching chemo. Don't do that. Chemo is like the tongue. The same tongue that can kill a person can build a person up. Chemo allows your partner to be rebuilt. That's a good thing.

You will feel like you've been placed on a conveyor belt and you can't get off. You can't. You must buck up and try to adapt to the speed of the conveyor. Sometimes, you will feel like Lucy. That's okay. There's nothing wrong with a little chocolate on your face.

So hang in there dear Caretaker. There will be time to sort things out. Feel all the feels and accept the help and do actually eat the chocolate.

The low low down

 

We like this journey to Tahoe much better than the journey we are currently on.

This morning, we decided together that we'll put it out there, a more clear picture of how Dominic is doing. You couldn't support us more than you already have, we've been so blessed. And I hate to weigh other people down, especially with family being so far away and feeling a bit helpless. We've struggled to know how much to share and how much to hold back. But, this is where we are. And NOT where we're staying. 😉 We== W

The combination of steroids and pain has ravaged Dom's body. He has lost over 40 pounds since May. He has also lost mobility due to such extreme weight loss and fatigue as well as muscle wasting that is a side effect of the steroids. We left the hospital in a wheel chair that one of our friend nurses found and gave to us. I think someone left it behind as it was missing the foot rests. The day we left, an aide jerry rigged a blanket to hold his feet up. This is in part why my mother's help was so tremendous. Me learning to open and fold a wheel chair and help him out of the car, with a jerry rigged foot rest. Wow! What an adventure I never would have signed up for, but since we're here...I'm all in.

We were given the impression we'd be given a wheel chair when it became apparent he'd need one, and didn't find out until the day we left that insurance wouldn't cover it. I bought one on line that was delivered to our hotel yesterday. So. Now we have 2! The foot rests on the new one fits both chairs, so we can choose whichever is more appropriate. (Different wheels on each). He's talking about taking the big wheeled one outside so he can get an upper body work out.

He also left with a walker, so picture me looking a bit like Dick Van Dyke in Mary Poppins with his one man band set up. I'm totally channeling that chaos energy as we make our visits to the infusion center. (How I wish I had Mary Poppins' bottomless carpet bag. That would solve a lot of problems.) As it is, I pack a bag with all our electronics and things we can't leave in a hotel in addition to files from work. I also pack a bag of necessities for him. I've got bags poking out on all sides and I'm carrying his walker while pushing him in his chair. We bring his walker so he can choose to walk or ride. He usually manages a bit of walking, but it's important to have a fall back. I made quite the entrance to the infusion center this morning with the new foot rest that I promptly rammed into the door jam. Thankfully, no damage done to Dom....but....extra length of chair, noted. I also laugh when I'm embarrassed/shocked/overwhelmed/worried/all of the above. Lots of necks jerked as I nervously giggled my way through the waiting room, literally hearing Bert's flat two note horn punctuate my shame

.

This is how crazy this whole thing is....before I left the week before to go home and pack, he was being discharged with a cane and a walker just as a precaution. In just one week, he slid back so far as to necessitate the wheel chair and hotel stay. I can't decide if I feel like a frog in slowly heating water, or if I'm shocked from jumping into an ice cold lake. I'm both?

He's very low, as anyone would be who has been through what he has been through. And, of course, the World Cup is over, so I just don't know how to entertain him right now. I'm so glad we're out of the hospital though. I think the anticipation of leaving was giving him anxiety, and bringing him even lower. As I mentioned before, I was also fighting against the nurses compassionately letting him not get up and walk. The prospect of leaving was definitely scary for both of us, as we'd only have ourselves to rely on. He did have a moment in the hospital where he had to be helped up. He couldn't clear a step in the shower and crumbled. We won't have that kind of help in a hotel. I still felt totally ready to get him out of there. I just know that the true healing won't begin until we're home, but being out of the hospital is the first giant step. 

There are so many logistics to this situation, sometimes I feel like a dog chasing its tail. For a while, it felt like an option to choose between renting a hotel room or going all the way back home. But, over the course of his last week at the hospital, it became clear that he can't handle the daily commute and a hotel was no longer an option but a necessity. I remembered all the endless searching on airbnb from before and just went straight to a hotel search. (I've since searched airbnb and nothing will work just now.) I am being budget conscious as well as mindful of our needs. We landed at an Extended Stay as it has a kitchenette and I was able to get a room right by a wheel chair ramp. Again...the dog chasing its tail. Things happened fast here and I was making decisions somewhat on the fly. When I made the decision to book at Extended Stay, there was still a possibility that Dominic could walk to and from the car with his walker, just not step over curbs. And I did not yet have an inkling of actually owning a wheel chair. (Let alone two!) Now that we have the chair, it frees me up a little as to where we'll stay. I would have possibly chosen something a little nicer if I was not concerned about long hallways and if he could eat from restaurants. I'd fantasized about room service and a hot tub while he recovered. Coffee in a styrofoam cup is about as luxurious as it gets. No room service, not even housekeeping.

And we are not staying here! I'm so glad I only reserved for 5 days because it is gross! So gross! It was good to land somewhere anonymous. But we've found our way to navigate this new life now. I'm a little bit panicking over germs and have my bleach wipes out all day long. I had some other hotels lined up, but my friend Kim is opening her door to us, and we're moving on Monday. I'm so grateful. I'd been concerned about several things bringing a nearly invalid person into someone's home, but she persuaded us. It will definitely be challenging to show up to someone's home with wheel chairs and walkers etc...but she's already cooking up some broth. So, we're in. And she might be an angel.

I was concerned also that the stomach pain is not going away. It's better, but still hurts. I worried that the treatment wasn't working, but was reassured yesterday that it will take some time before he's feeling better. I mean, that's not a reassurance, I hate that he's in pain, but I don't need to panic over everything right now. It seems by other signs that the ATGAM worked.

It's going to be a looooong road back. Gvhd is no joke. No joke. It's like we're experiencing a whole new disease and prognosis. And it's been the worst part of the whole experience. I guess we got a little too saucy after the transplant and he was walking miles every day. 

But we'll get back to that. Little did he know when he married me that I am a task master and there's no fetal position when our future is on the line. We are going to face this newest challenge head on. I have to dig real deep on this one. When I ran out for groceries while my mom stayed with him, I couldn't think straight at all. I was beyond exhausted from lack of sleep and the whole deal. I knew I wanted to make coffee in the room, and there wasn't a coffee maker. I have our aeropress with me, so all we'd need is hot water. I was so hitting a wall that I couldn't think about just boiling water in the microwave. I also didn't realize the hotel would provide a coffee maker. (Ew?) My friend offered to loan a tea kettle, and though she lives literally minutes from the grocery store, I could not even go pick it up. I spent $10 on a really ugly tea kettle because I was just that tired. That's what things are like right now. I'm trying to manage everything and meet our needs and anticipate our needs and it's like a moving goal post. Any extra decision I have to make or logistics can send me over the deep end. And yet, I must make them. I know people will have extra helpings of grace for me just now.

And yes, continue to pray for me!!! I know he's the one who needs all the healing energy. But. The couple across the hall from us was telling their nurse, (loudly enough that I could easily hear) that the wife had been bitten by a brown recluse spider. He was in the hospital receiving treatment, and she woke up in a hospital five days later after passing out from the bite. I guess there's still a huge open wound on her leg. Yikes! What an ordeal. Trying to stay healthy here!

I am getting abs of steel from helping Dom in and out of the car. Seeing as how I have gained approximately what he has lost, I'm happy to feel those muscles again. He doesn't recognize himself right now. I do. I still see him. I can't wait to have him back in all his fullness. I miss him not being in survival mode. Soon, this will be a distant memory. Until then, I am his lifeline. I will eat the chocolate and get things done. (Because I am also doing quarterly taxes for work in the midst of all this.) I will help him with his shoes, until he can do it again himself. I will lovingly prepare the smoothie, even if he just can't drink it all. I will carry the bags and the walker and measure out his prescriptions and do whatever it takes to get him back in the real world again; to get him back in his body and to get us back home, and celebrating with you. 

I can do all things.
But I could never claim to do them alone.