It is done.

On Friday, April 28th I finished (what I hope is) my last round of chemotherapy.

I struggle to find the words that will fully explain what the last four and a half months have been like. What they have meant to me. What they signify.

I’m not exactly sure what to say which is more likely because I haven’t even begun to process the depth of trauma that has occurred.

The last few days have been so unbelievably hard and this last round of chemo destroyed me until eventually there was a light again. A twinkle. A glimmer of hope appearing in the distance, anchoring me back into reality.

In the darkest moments this past weekend, when fever crept in and a rash so dark and red, swelled my face and body so I felt unrecognizable, I kept telling myself it’s done in an effort to stay above the surface. This part is done now and I’m grateful for that.

As joy washed over me because of that very reason, I also realize how much grief and sadness sits in my chest too. That and the recognition that I am going to have to figure out how to navigate this in a way that doesn’t swallow me alive.

I will not lie. I feel a wave of horrible sadness and emotional pain that frightens me. I feel exhausted. I feel overwhelmed. I feel confused and numb. The last five months I have been in soldier mode just trying to get through the side effects of chemo all while trying to still work a bit here and there and stay as present in my life as I can.

I have so much to write. So much to say but the words still evade me and I’m left doing the delicate dance of processing while also moving on, moving forward.

I know my physical self will return. My hair will grow back, I’ll lose the ten plus pounds of chemo weight I gained, I will regain my strength, my stamina.

The hardest part, in my opinion, is lingering in the near distant future and can no longer be avoided by telling myself I’ll just deal with it once chemo is over. Navigating the emotional stuff.

Trying to figure out how to be in the world again. To deal with the aftermath of what I just went through and will continue to go through over the next few years with immunotherapy and scans and just, well, waiting to see what happens. This part is the hardest. This part hit me like a Mac truck last time, sideswiping me from out of nowhere, dragging me miles into the painful places I didn’t want to go.

I’d be lying if I said I didn’t feel like a big part of my life was just one of constant waiting. Waiting for cancer to sneak back into my life the way it does every few years, and, like a wrecking ball, leveling my world to the ground once more.

The constant stop-start of it all is so exhausting. The expectation to “put it all behind me now” weighs heavy on my shoulders because that part has never come easy to me.

I’ve talked about it before as feeling like I am standing in the middle of time square as the world rushes on around me. I feel like a fish out of water, trying to take in a deep breath of air only to realize I don’t know how now that I’m am above the murky, wet layers that have, in a way, kept me safe for the last few months.

The next step is to get scanned in three weeks and then from there, continue on with immunotherapy for two years but I already know I’ll have to take this treatment-by-treatment. I’m tired of feeling sick and I’m tired of feeling like a stranger in my own body. I’m tired of giving my time to sitting in a chair and then to being hit by the side effects a day later.

I want to live which is ironic because immunotherapy is the best chance of me doing that for the longer haul yet, I fantasize about quitting it all every single day. Ripping the knobby port out of my chest and never looking back.

I’m exhausted.

And scared.

Because as much as I hated every minute of treatment, there is a protective layer being in treatment brings with it.

A hope.

A comfort that this thing that is poisoning you, altering your appearance, your stamina, your whole life, is also poisoning the cancer. It makes you feel safe. Like for the time being you have tiny workers inside your body fighting on your behalf and now their job is done and you have to wait and see how well their work will hold up. You wonder and hope they laid a strong enough foundation.

And, only time will tell.

But history and time have shown me what happens.

When my tiny monster returns.

And those are the fears I must grapple with.

On my own.

This Too Shall Pass

On Friday, January 13th, I began a journey I would never wish on anyone. I had my first infusion of chemotherapy and immunotherapy. This week, to put it bluntly, I’ve been a little worse for wear.

It’s funny, I had these grand delusions that I would be back up and working in just a few days. I can do this I thought. I’ve been to hell and back before and I always bounce back quickly. I will with this too.

This beast however, is one I have yet to experience before. This beast, has annihilated me, leaving me question so much already.

I’ve been dealing with neuropathy that is so painful I don’t quite have the words to describe it other than feeling as if my nerves are being ripped apart by electrical shocks and waves every few seconds. This began Sunday evening and has yet to leave. And that alone is terrifying. To think of a life riddled with this kind of pain.

I hear the second week is better though and the third well, I welcome that with open arms as it teases me with thoughts of being “almost normal” again. Yet, I know when I finally make it to week three the clock starts ticking again until I’m sitting in that same chair, in that same cancer center, getting those same drugs pumped throughout my body. Round two.

And the cycle begins all over again.

I’m doing my best to hold on to little moments of joy, although few and far between, and my mantra, although hard to fully believe, this too shall pass.

This too shall pass.

And I pray that it does and that this time next year I’m pain (and cancer) free.

I hope the rumors are true though and next week I’ll feel better and the following more like myself and I can get back to work in whatever way that may look like for the foreseeable future. I miss my craft. I miss creating and putting my thoughts into action. I miss the chatter of a podcast playing in the background while I get lost in my shop.

I think one of the most uncomfortable parts of all this is the not knowing. Not knowing when life will feel normal again. Not knowing if or when I can work again. Not knowing if this pain will subside enough for me to do the things I love dearly. The things that make me who I am.

All I can do is the very thing I’ve been trying to figure out how to do my whole life. Surrender.

Surrender, surrender, surrender.

And wait.

And just be.

And that, my friends, is an art in and of itself and I haven’t really learned that medium yet. But like with all my other artistic paths, practice makes me better and better. So, I’ll practice this too.

And eventually, this too shall pass.

xo, amanda

P.S. - Ongoing help is probably going to be vital until I figure out my new flow with work. I’m so grateful to you and to all who have supported me in the various ways laid out in my Cancer Gift Registry. It’s truly lifted me up and made me feel so loved.

You can find that registry here.

One year later - this is what a year of cancer looks like

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There will come a time when you believe everything is finished. That will be the beginning. - Unknown. 

 

 

 

 

I've tried really hard to find the right words to share what this week means to me but I'm falling short. 

What I really want to say is thank you. 

Thank you for supporting me and holding me up when I was unable to do so on my own. 

Thank you for allowing me to be so raw and authentic and feel safe to bare my soul during this difficult time.

Thank you for laughing with me while I'd find my way out of the darkness and back into my funny and sassy self. 

Thank you for all the notes, messages, comments, flowers, gifts, dinners, prayers, good thoughts, energy, and most importantly, love. 

I truly would not have been able to do the last year without you. 

I don't know what the future holds and to be honest, whatever comes my way I know I'll handle it just the same. 

Often you read that difficult times will make sense down the road. I'm not sure if that is always the case. Some situations just never make sense. However, I know for me, it is. All of this is starting to make just a little more sense. 

Most importantly though, this last year has taught me just how important it is to have faith and to be okay with asking for help. 

I did my best to document the year in photos. One thing was consistent, as much pain I was in, I often found myself smiling. A lot. And that felt really nice. 

To many healthy years ahead. 

This is what a year of cancer looked like. 


A few days after being diagnosed...a love of my life found his way into my heart. 

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I had a real life Grey's Anatomy experience with a room full of interns...

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I was surrounded by love and friends who give uplifting gifts that make your stitches hurt from laughing...

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Family came to visit and take care of me and I got the most amazing one-on-one time with my sis-in-law...

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And my older bro...never finished that chicken coop though :) 

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I had lots of pokes, prods, needles and procedures. So many. 

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But I had my first art opening...

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And a trip to Joshua Tree...

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And a drive north to Seattle...

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To be with the three other loves of my life...

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I walked into my first day of treatment ready to face it all...

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And then flew to Miami a few days into treatment and found a few days of solitude...

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My favorite part was crossing each treatment off...

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And just like that, six weeks, five days a week...was finished. 

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And I turned that page...

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And took myself to Idyllwild for my birthday, rented a little cabin in the woods and hiked for the first time since treatment ended...

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Sadly, I lost the other love of my life. 10 1/2 years together and I will never forget his love. 

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And I met my women for our Red Tent. I didn't leave this spot all weekend. 

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Spent Christmas with my soul sister...

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And enjoyed life.

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that's a wrap