Do Epic Sh*t

Riding the cancer rollercoaster can be exhausting. Things go from bad to worse to good to great all the time.

Sometimes it is in a day.

Sometimes it is in an hour.

Sometimes we live our life moment to moment.

Our motto of #rollwithit is really about being open and remembering everything is temporary. The bad moments will pass and the good ones come along for us to savor and embrace.

There is no balance. It doesn’t exist in our world. Moments go from complete darkness to blinding light.

Sadness to happiness. Fear to hope.

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Last week I had a long meeting with Logan’s oncologist about her recent MRI and we discussed realistic goals 😩😩😩 and this week we spent and entire day with Johnny Depp. (For real!?!?! WTF!)

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How does one even process the insanity, inconsistency and contradiction that happens to be our life?

It is crazy.

Log’s MRI was filled with good news but there was also some really bad news.

I left the meeting with our oncologist feeling torn and somewhat broken yet incredibly hopeful and optimistic.

In one sentence I was told her scan was mainly stable with some mild continued improvement in the right anterior pons (the area of the brain we are pretty sure has caused her sudden decline). I was on cloud nine.

And then, just as quickly I was given the bad news and my hope was ripped away.

Her organs are in distress and it is unclear how many more doses of chemotherapy she can endure. There is concern for her liver (god only knows I thought we’d be having a discussion about mine first😩🍷🍷) her bone marrow, her kidneys and her lungs.

Almost 300 doses of chemotherapy is taking a huge toll.

I could go into a ton of detail about what this means but basically what it comes down to is a balance between killing the cancer and not killing your child.

Juliette (our oncologist) encouraged me to really think about what ‘goals’ we as a family, have with this treatment.

She encouraged me to reach out further to Canuck Place for support and respite.

To Prepare.

She discussed the uncertainty of what might lie ahead.

She reiterated the reality that a ‘cancer free’ life is not likely and that chemo is not a cure.

She reinforced what we already know- we are simply buying time.

What the time looks like and how much we have is still anyone’s guess.

She told us we’d reached a fork in the road.

There is no choice but to lower the dose of chemotherapy to protect Logan’s organs from failure. She also gave us the option of stopping treatment altogether.

She assured me in our situation there is no right answer and there was no way I could ever make a wrong choice.

I felt like someone punched me in the gut.

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“But, she is doing so much better” I said.

She agreed.

I threw around different and obvious scenarios about what would happen if we stopped treatment.

I felt so puzzled

“So, the MRI looks better and clinically Logan is doing much better, so it is pretty safe to say the chemo is working, right?”

She nodded again.

“But if we continue giving her chemo she may go into organ failure or we may do irreversible damage and then we may end up a totally different shit creek?”

Again, the same nod.

“This is where it gets tricky. It is a delicate balance. There is no right or wrong now. This is where we talk about goals and dreams and hopes and what you, as a family, want to achieve.”

She tried to be encouraging and humorous, reminding me of how many times she had been wrong and Logan had beat the odds but it didn’t work.

I know this time is very different then any place we have ever been. She does too.

I started to cry.

“I don’t want to talk about fucking goals- especially with you.” a primal squeal escaped my mouth.

She didn’t say a word.

“I mean, I hate talking to you about goals because I know you think our hopes and goals and dreams are impossible and telling you makes me feel crazy and slightly delusional.”

I paused to look up at her. I could tell she was trying to holding back her own tears.

“You have no idea what this is like. I see you every few weeks or months and you don’t get to measure our life with pictures or blood tests or exams. Your goals are not the same as ours.”

It remained silent and she looked really sad. I could tell she knew saying nothing was best.

She has had this conversation many times before and she has experience navigating it. Knowing this infuriated me.

“You don’t know how hard this is. You get to do your job and go back to your healthy kids and your great f’ing life”

I felt bad for attacking her. I know logically this isn’t her fault but I couldn’t stop myself.

“When we lay in bed at night as a family, we don’t talk about Logan dying. We talk about when she gets better and what our next adventure will be. We talk about Logan being well enough to take a trip around the world. We laugh about running away and having so much fun together. We talk about all the places we want to see together and the cool shit we still want to. We talk about volunteering in Africa and eating gelato for breakfast in Italy and doing yoga in Bali. We talk about Jared quitting his mundane job that he has been forced to keep to pay our stupid bills and we talk about Brody blowing off school for a year and getting a real life education. What we talk about is forgetting about this bloody hospital and cancer and this whole life. We talk about checking out, and taking a freaking break and regrouping. We dream about freedom.”

At this point, I was crying so hard I had full blown hives and snot running down my cheek. I was slobbering and stuttering and shaking.

“We want Logan to get better enough so we can go travel for one solid year. That, Juliette is OUR secret, private fucking goal!!!! We want ONE month away for every year she has been sick, 12 months for 12 years, and I hate that I am forced to sit here in this windowless room and listen to you discuss trips to Canuck place when I have been telling my kids our trips are going to be to see the orangutans in Borneo.”

I paused to catch my breath.

“I don’t know if I am in total denial or if cancer has made me half ass crazy or if you just aren’t on our side or if you don’t ever really see us at all?”

My tone softened “How can you not already know our goals? It has been twelve flipping years? Life all over the map is our fucking goal!”

I let out a long sigh and a slight moan and I looked up from the ball of Kleenex I had torn apart in my hand feeling slightly ashamed of my language.

She was smiling and her words were comforting. The energy shifted.

“Well then….. I guess we don’t need to discuss any more goals today. You clearly already have them. Please, do try to consider taking a little more down time at Canuck place. This is beyond exhausting and at the very least you deserve a cooked meal.” She wrote some notes in her file. “But in the meantime, we will need to start teaching you and Logan how to change her feeding tube without nursing assistance. I assume she’s going to continue to need it for the unforeseeable future and a G tube insertion won’t be great option if she wants to swim in the ocean on her trip around the world. When it is time I will reach out to my colleagues in different countries and see what they can do to help you get the medications you will need. If we can, we will figure out this plan and work towards your goal. What is your timeline?”

I couldn’t answer because I was so shocked.

Juliette is never like this.

EVER.

She is cautious beyond reason and maybe she just threw me as a life line to keep me from a complete meltdown. I don’t know, or care, because I love her for it.

Just like an alzheimer’s patient doesn’t want to hear they are confused, a cancer mom doesn’t want to hear about a life with out their child.

She said exactly what I needed to hear. She would try to work with us. That is good enough and I won’t ask for more.

We notched out a loose plan to move ahead with another round of chemo, albeit a lower dose, and continue to monitor her organs a little more closely while planning our epic around the world tour. We will aim to get Logan strong enough to leave sometime within the first six months of 2018.

We left the hospital and went straight to Staples and bought a map.

IMG_8363Maybe this is just a dream.

Maybe an around the world trip might never happen and maybe we are crazy for even thinking it can but we are going to plan for it anyway.

It gives us something to daydream about, something to hope for and something to strive to work towards and something to talk about. The ultimate 90 day plan.

It is our own personal, perfect and insane goal.

I honestly don’t think it will be that hard to achieve. I mean wejust have a few hiccups to work through….

  1. Cancer
  2. Treatment
  3. Medication
  4. Work
  5. School
  6. Money!?

No biggie, right?😉👊🏻

In the meantime, we will continue to live in this moment. We know its not all about the big stuff. The everday stuff is what really matters and we aren’t going to let it pass us by. Living  the best life we possibly can means finding fun and possibility and opportunity and comfort in the mundane.

None of us will ever be able to know in advance what life may bring.

One day you could find yourself planning end of life bullshit and the next day you have to pinch yourself because some A list celebrity is sitting next to you wearing a hat with your website and motto on it telling you dreams can be become possibilities and to just look at him and continue to believe and not give up hope. Ummmm- ok 😉

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I feel so mixed up.

The past 7 days have been a whirlwind of extreme emotion and everything feels surreal.

Super highs and super lows.

I reached out to my good friend and tribe member Heather for comfort and advice. She is a cancer survivor, a brilliant mind and one of the kindest hearts I’ve ever met.

It took her a few days to respond to my news about Log’s MRI but when she did her words were perfect.

When I was a little girl, I remember learning about the Buddhist practice of perfecting sand art- only to brush it all away when finished. I remember being baffled by the triviality of this act and scoffing at the perceived waste of time. As I’ve grown older my thoughts often return to this practice and I feel I understand it more and more.

We spend the time gifted to us constructing these beautiful intricate lives and it feels like such a cruelty when the artistry is swept clean. We want to hold on to what we have created, to keep it close to us because is so lovely and we’ve worked so hard on the construction. And yet it is the action of creating that matters in the end- not what remains.”

And so we will… simply, continue to create.

This life.

Our life.

As it is today and for what we want tomorrow

We will plan.

We will dream.

We will hope.

We will allow the artistry to be swept clean when it needs to be and then we will start fresh once again.

We will continue to #rollwithit

Because, after all, it is the only thing any of us can ever really do.

Much love,

J❤️❤️🤞🤞

P.s. Yes, Johnny Depp is super rad and Logan has decided he’s basically her boyfriend now. 😘❤️

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Some things never get easier~ MRI day.

It doesn’t matter how many times I have sat in the MRI waiting room, I always feel panicked.

I don’t know why but every single time I enter that room there is a sudden pulsation of fear that overcomes me and I literally feel like I am going to lose my shit.

The MRI waiting room isn’t a scary place and theoretically it isn’t any different than any other waiting area in the hospital but it doesn’t matter. I loathe this room and almost choke on the lump that forms in my throat every time I have to sit in there.

Maybe, because I know even though it looks the same as all the others, it is different.

It is a room that carries a hefty, weighty, stressful energy and I sense it in every fiber of my being.

It is where families go to measure progress or confirm their worst fears.

No one gets an MRI because something isn’t wrong.

An MRI is a big test and it holds clout.

Despite any pacifying from doctors, the pictures that come from the scan make almost all the treatment decisions.

Knowing this means I can almost feel the banging of the machine through the thick painted cement walls when they fire up the machine.

The thud of the metal door from the waiting room to the radiologists desk seems to close harder than any other door in the hospital and every time it does I consciously think to myself, “You have to let it go Jenny. It already is whatever it is going to be. ”

Only I never can just let it go.

It is impossible.

Instead, I stew in my fear and worry and sit in that room which feels like torture and limbo combined.

It is hard to explain the intensity of the wait between a scan and the report but if you have ever experienced these moments, you will know what I mean.

I used to go into the scan with Logan every time she had one.

I used to think I could tell by the facial expressions of the technicians what the pictures were showing. I used to drive myself crazy trying to see a reflection in the glass between the machine and the computer screens as the images appeared.

I used to be so desperate to know the results, I felt like I was going insane from the sound of the machine as it began to hammer.

Now, I just sit silently outside in the irritating, confined waiting room trying to calm my own nerves.

I don’t exactly know why or even when I decided to start sitting outside the scan but today I realized it is no easier than being beside her.

It is all I can do to not to throat punch the parents who turn The Wiggles on the TV full volume while ignoring their kids who are throwing around plastic toys and playing the xylophone.

It is all I can do but wonder, “How the fuck does one cope with this? How the fuck do I cope? Am I even coping?”

MRI day and business trip= no coping and no shoes 😳

Today, I tried to be super evolved and self aware. I  journaled my way through my stay in the MRI waiting room. I was in the midst of writing through my feelings of why the room freaks me out so much when it all hit me.

I had just run into DR. Rod in the hall.

The kids and I were taking a selfie outside the MRI room when he came up and joked about our lighting and our angle.

“Where are you off to?” I asked him

“ICU.” He replied with a slight head tilt.

ICU is shittier than MRI. We both know it.

I looked down the long hallway with the stars on the wall indicating the route.

We’ve been there.

Actually, I think we’ve left MRI and very quickly been admitted into the ICU or vice versa.

It hit me like a ton of bricks.

MRI is so fucking scary because it is the moment when you realize the magnitude of the situation you are facing.

MRI reiterates that you are caught between living life (and walking out of the front door of the lobby) and facing death (and heading down the hall to follow the stars to the ICU)

So, it is just “holy fuck!!”

MRI should be scary simply because it is…..

Super Scary. Period.

And another scan is now done and yes I am typing this while drinking a glass of wine.🍷

This glass of wine is from a neighbor who left me bottle at my doorstep because she totally  knew I would need it tonight. Thank the dear lord for moving me next door to Lesley.

Believe it or not I am not as nervous about this scan as I usually am.

I think I know what to expect.

Logan is doing better than she was, but she is also a long way from where she needs to be.

We are just plugging along (having as much fun as we can, when we can). Which is all I think we can do at this point.

I really am expecting a ‘status quo’ report.

But expecting and wishing are two different things and the crazy thing is, as I write this I am reminded how I don’t know what to wish for.

Of course, I wish her cancer would just disappear.

I always do and I’d be a shitty parent if I didn’t, but what if tomorrow I found out it was all gone and this Loggie is the Loggie we were left with.

Would it be enough? Would we feel like we  had won the battle?

Logan is so far from where she needs to be.

Could I accept where we are at today as the ultimate success and rest of our lives or as I sit here tonight should I be wishing to find out Friday we are only making progress on the road to the cure?

I don’t know.

What I truly wish for is for a life that wasn’t ever about cancer.

I wish this disease wasn’t part of our personal equation, but it is.

And reality has a shitty way of being real so there is no point in wishing for something that can’t be possible.

So, what I am left with is I don’t know what to wish for and I have finally decided that is ok because sometimes wishing is just a recipe for disappointment.

Maybe my therapist will help me to better understand this question.

Poor thing had a cancellation tomorrow and called me in at last minute.

My first thought when I got her message was “SCREW YOU UNIVERSE!!!😩😩😩.” But then I also said a silent thank you.😉

Good timing. I know I need it.

Results come Friday and the day between the scan and the report can be a doozy.

On that note, the new hospital is almost built and ready for patients to move in.

Do you think it is too late to suggest they make sure the MRI machine is no longer next door to the ICU?

 

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