The Small Cell Chronicles: Lexi Brady’s Cancer Journey

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August has been incandescently wonderful.I swam in the ocean beside sea turtles. I laughed with Manon until our sides we...
29/08/2026

August has been incandescently wonderful.

I swam in the ocean beside sea turtles. I laughed with Manon until our sides were splitting. I took calls with wonderful people in the writing community about projects quietly taking shape behind the scenes. I signed onto a new project with one of the top artists in comics as head writer, with much more to come on that soon, and received the first batch of illustrations for my upcoming poetry collection.

For the first time in over a year, I read my work aloud at the Writers' Colony at Dairy Hollow, an institution that has cradled my creativity for twenty years.

I will return there for a workshop in October featuring Melissa Carper, and in just eight weeks, two of my scripts will carry me all the way to Hawaii, where I will have the extraordinary privilege of working directly with writers and directors I have admired for years.

And, of course, there was treatment.

This month brought a series of additional tests as my body began developing side effects from immunotherapy. My insurance renewal has now been denied, so I do not know exactly what lies before me or what the coming months will ask of us.

But tonight, uncertainty is not the largest thing in the room.

Gratitude is.

For the sea turtles. For the breathless laughter. For poems becoming pictures and scripts becoming plane tickets. For the people and places that continue to cradle my creativity, and for a life that, even now, keeps finding new ways to astonish me.

Now I have to get back to my emails. I have some very exciting things to send off.

The chemo curls are really curling now 🥹After months of waiting and watching, seeing my hair come back fuller, longer, a...
15/08/2026

The chemo curls are really curling now 🥹

After months of waiting and watching, seeing my hair come back fuller, longer, and entirely its own wild little thing feels like being handed a piece of myself again. I didn’t realize how much of my identity lived here until I began recognizing myself in the mirror again. 🥳

30/07/2026

My new reality.

Every 21 days, I return for immunotherapy.

Between those appointments are labs, scans, bloodwork, urine tests, waiting rooms, phone calls, and the peculiar rhythm of a life measured in medicine.

Unless science makes another leap forward, I will likely never ring the bell that marks the end of treatment. My life is tethered to a hospital now. That is simply the truth of it.

And yet.

I refuse to let that be the only truth.

I am staying as hopeful as I know how. I am making every day between appointments count. I’m writing the books I’ve always dreamed of writing. I’m creating art. I’m doing physical therapy because I still believe there may come a day when my body will carry me across a dance floor again.

I still have far too much left to do.

I have stories to tell.

An Emmy to win.

Performance art that will probably make people wonderfully uncomfortable.

People to love.

Places to see.

A life that still deserves to be lived in full color.

I am still stage IV.

There are still tumors scattered throughout my body.

But immunotherapy has already shown shrinkage, and I refuse to surrender the space between today’s reality and tomorrow’s possibility to fear.

I don’t know how many years I have.

None of us really do.

What I do know is that I intend to fill whatever time I’ve been given with wonder, with work that matters, with laughter loud enough to echo down hospital hallways.

My faith has steadied me.

My family has carried me.

My friends have loved me through days when I couldn’t stand on my own. The older I get, the more I understand the story of the footprints in the sand. There have been so many days I wasn’t walking at all—I was being carried.

So this is my reality.

Not a tragedy.

Not a surrender.

Just a different road than the one I expected.

And if you know me, you know one thing already:

I’m a stubborn little s**t.

Cancer is going to have to work a hell of a lot harder than this to convince me to stop living.

02/07/2026

There are moments in life that reveal just how deeply human beings are capable of loving one another.

This past year has been one of those moments for me.

When I look back over the last nine months, I don’t just remember hospitals, infusion chairs, blood draws, and scans. I remember every hand that reached toward me when I needed one.

You prayed for me.

You donated when you could.

You shared my story.

You sent flowers, meals, kind messages, encouragement, and love into some of the darkest days I have ever known.

There is no version of this story where I am here without all of you.

Your generosity did more than help me afford treatment. It gave me time. It gave me hope. It reminded me that even in the most frightening seasons of life, we belong to one another.

Thank you will never feel like enough.

Immunotherapy has been an incredible gift. My hair has begun to grow back, slowly and stubbornly, and every new curl feels like a quiet promise that my body is still trying.

I still have a long road ahead of me.

The cancer has not disappeared. I continue to live with metastatic spots throughout my body, and with them comes the pain that many of you know has become part of my daily life. My current treatment plan includes at least two more years of immunotherapy, and I carry the hope that somewhere at the end of this chapter I will finally hear the word remission.

This month brings another season of testing. I will undergo fertility assessments, full body MRIs with contrast, and what feels like countless vials of blood as my doctors continue mapping out the road ahead. Some of these tests and scans, particularly portions of the fertility workup, are not covered by my insurance, but they are important in helping us understand what my future may hold.

I try very hard to make the most of every day I am given.

Some days that means creating, writing, wandering somewhere beautiful, spending time with the people I love, and soaking in the ordinary moments that once felt so far away.

Other days, making the most of the day simply means allowing my body to rest. Some days healing looks like sleeping. Sometimes the only movement I manage is from my bed to the couch and back again.

I have learned that those days count too.

This past week has carried a great deal of anxiety and grief.

For so many months, survival left little room to process what was happening to me. Every ounce of energy went toward getting through the next appointment, the next infusion, the next scan.

Now that life has grown just a little quieter, my heart has begun catching up with everything these last nine months have held.

I suppose that is the strange thing about surviving. Sometimes the grief waits until you are finally safe enough to feel it.

Even so, I remain profoundly hopeful.

Hope isn’t always loud. Sometimes it is as quiet as new hair growing in. Sometimes it is taking another walk. Sometimes it is showing up for another infusion. Sometimes it is believing there are still beautiful things waiting for you on the other side of all of this.

Thank you for helping me keep believing.

Thank you for every prayer, every dollar, every share, every message, every kindness, and every moment you chose to carry part of this burden with me.

You have changed my life in ways I will spend the rest of it trying to honor.

For those who have asked how they can continue supporting me through treatment and the testing ahead, I will leave my GoFundMe in the comments. Whether you are able to give, share it with someone else, or simply continue keeping me in your thoughts, please know that every act of kindness has mattered more than I could ever express.

With all my love and endless gratitude,
LLAP

Lexi

Today for Lexi's Immune Therapy Treatment her favorite cousin Steven is with us since he is on spring break! He is the b...
16/03/2026

Today for Lexi's Immune Therapy Treatment her favorite cousin Steven is with us since he is on spring break! He is the biggest sweetheart and we are grateful for him. He is 15 years old, brilliant, but above all a kind huMAN being. Stay sweet Steven always!

Lexi will be crushing treatment and the cancer as usual.

And I, well, I will be here always and forever Lexi.

Love, Auntie T / Momma aka Tracie ❤️



PS Thank you to everyone for following my sweet girls story. We can still use help, and I will post the gofundme in the comments. Love, Light and Laughter to all.

When Lexi was 7, her school had one of those reading programs; for every book test you passed, you got a personal pan pi...
16/02/2026

When Lexi was 7, her school had one of those reading programs; for every book test you passed, you got a personal pan pizza coupon to Pizza Hut. Most kids used their computer hour to play games. Not my Lexi. She used hers to take tests. Stack tickets. Earn every slice.

One afternoon I was big and pregnant with Ava, waiting in the pickup line, when I saw another girl demanding Lexi hand over her pizza tickets. Before I could fully process what was happening, that girl threw Lexi against a wall and ripped my baby’s earring clean out.

Hormones or not, I went full mama bear. I’m pretty sure I yelled, “Get the f**k away from my kid,” which wasn’t received well by bystanders, who mind you, had not intervened. I pulled that girl off my daughter.

In the car, Lexi sat there with her stack of Pizza Hut tickets still clutched in her hand. I told her I was proud of her for standing her ground. She told me that if the girl had asked nicely, she would’ve given her some, but that she’d been saving them for us because babies cost money. She wanted to help. She wanted to contribute.

Always a lover girl. Always thinking of her family. My angel.

A few months after Ava was born, we were probably on our 900th personal pan pizza (it had officially become obnoxious), when an employee came to our table to tell me I couldn’t breastfeed in public ;even though I was fully covered with a blanket.

Before I could respond, Lexi did.

She asked him why he wanted a baby to go without sustenance. (She was a reader always using words that made me blink like, okay kid.) When he told me I could feed my baby in the bathroom, she said in her sweet little voice “h-e-double-hockey-sticks” no, that babies shouldn’t eat where people p**p because that’s unsanitary.

Chris finally stepped in and said, “Lex, it’s okay, let’s just go,” and that was the end of our Pizza Hut era.

But that fire? That never left her.

Lexi has always been a champion; for her sisters, for wildlife, for strangers, for anyone who needed someone in their corner. She would have stood on those Pizza Hut tables and rallied a crowd if we’d let her. Fierce. Strong. I sometimes think she was channeling our ancestor Grace O’Malley.

And now here we are.

The hospital called this week to tell us Lexi is eligible for something extraordinary. Only 1 in 10,000 people qualify for this personalized immunotherapy treatment. Cutting-edge. Sitting at the forefront of modern science.

They will take a piece of her tumor and some of her healthy cells and create a drug designed specifically for her body to target and eliminate this cancer. And once she is tumor-free, this treatment can give us up to a 90-day warning if the cancer even thinks about coming back.

She still has part of the primary tumor, and we’re wanting to see it shrink over the next few cycles. But this Friday, Lexi goes to Stephenson and her team will send off the samples to begin creating this incredible therapy.

Seven-year-old Lexi stood her ground for pizza tickets she was saving for her family.

Now grown-up Lexi is standing at the edge of breakthrough science.

1 in 10,000 people have this biomarker, and there have been less than 5000 women to ever have this cancer. Special doesn’t even begin to describe Lexi.

Love, Mom

PS don't forget us, we need your support. It truly takes a village.

https://www.gofundme.com/f/help-lexi-fight-stage-3-small-cell-cervical-cancer?attribution_id=sl:446ab2bd-533b-4456-b561-ddbf7f0080d2&lang=en_US&ts=1760889953&utm_campaign=man_sharesheet_dash&utm_content=amp17_ta&utm_medium=customer&utm_source=copy_link

02/02/2026

News from my latest scans & labs 🤍 Just got labs drawn this morning at the hospital & I’m so happy right now.
My main tumor is now about half the size of when I began treatment!!! The meds & my body are working in overtime, but im making this cancer my ***** 💕
I’ve felt so held by my community through this, in ways I’ll never forget.
2026 is just beginning, and so am I.

She already did this. I hope she knows. She is such an amazing person whom I am so proud to know.
31/01/2026

She already did this. I hope she knows. She is such an amazing person whom I am so proud to know.

We are here at OU Health Stephenson Cancer Center for Lexi's first round of chemo in the new year. Today she will do thr...
05/01/2026

We are here at OU Health Stephenson Cancer Center for Lexi's first round of chemo in the new year. Today she will do three different chemo medications, and the rest of the week her treatments will consist of just one chemo medication per day. The past few months Lexi has been relentlessly funny and fierce, facing this with a grace, that she struggles to see within herself. I am so proud to be here with her and help her during this time in her life. Just like most mothers I love my daughter with all of my heart and soul. And I believe we can get through this and give Lexi the life she deserves.

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