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  • About
    • My Story
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    • Fun Facts
  • Speaking
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My Journey

Define Fine

March 15, 2018 by Stacy Hurt

It’s easy, right?

Fine. It’s a word I’ve come to mostly despise.  As in me posting my 30th chemotherapy session on Facebook, and a friend from college commenting, “It will be fine.”  I called my best friend sobbing; “Of all of the things that having poison pumped into your veins for the 30th time isn’t, it’s fine.”  (By the way, that was 25 chemos ago…)

Or as in a colleague seeing me at the grocery store and asking, “How are you doing?” I replied with my stock response, “I’m hanging in there.” And then she says, “But you had a clear scan, so you’re fine, right?”  I couldn’t even deal with that, so I just responded, “I wish it were that easy.”

Or running into a neighbor at breakfast, and her celebrating my recent chemo break, which has been nice.  She asked, “So how are you doing?” I said, “I’m using this time to rehabilitate my life from all of the damage from cancer and chemotherapy.” She stared at my blankly, threw her hand at me, laughed, and said, “Well you look great, so I’m sure you’ll be fine.”

I don’t provide these examples to diminish the good intentions of well meaning, caring people.  I provide them to illustrate the complexities of cancer and the fear that cancer evokes.  To be blunt, people either have you “dying” or “fine.”  If people are concerned that you’re dying (a metaphor for existing in a very fragile state) then you get cards, texts, calls gifts, and herculean efforts of support.  If you’re “fine” (a metaphor for magically cured), then you’re off their radar – compartmentalized into the “I don’t have to worry about her, so I’m moving on to my next thing – like how to get my kid to soccer practice.”

The good, the bad, and the ugly.

To address the fear part:  Cancer IS about the scariest word in the English language.  You don’t want it, you don’t want to hear it, and unfortunately a lot of people don’t want to be around it.  My heart always goes out to my atheist/agnostic cancer warrior friends who post on social media about their complications, and they get the comment of “Prayers.”  Unfortunately, in their world, prayers don’t do much good for them.  I’d much rather see a comment of “Meals” or “Laundry” or “Errands,” meaning “I won’t offer you prayers since you don’t acknowledge those, but I WILL offer you meals, laundry, or errands.”  It seems like any of those three would go a lot further for those folks.  Is it easier to just say “prayers”?  And then some folks don’t have to deal with the ugliness of actually being around cancer and witnessing first hand its deleterious effects?  Is it plain and simple a cop out?  I’ve been blessed and fortunate to have received all of the above, and all have worked wonders for my recovery.  I just think that the contribution should suit the one in need.  And being a true friend means knowing that person’s belief and value system intimately enough to give them something that would actively promote their healing.

It leads to a larger discussion of dealing with good news vs. bad news.  We see on social media that images of puppies, beautiful people, and joy get the most “likes,” while suffering, despair, and despondency get crickets.  I’ve seen this first hand on my posts.  When things are good, everyone is happy.  When things are bad, no one knows what to do and they panic.  Panic most always leads to ineffective behavior or even no action whatsoever.  When I post bad news, and I get zero response, I feel lonely, unloved, and abandoned. What bridges the gap?  Education.  I used to get angry and frustrated.  Now I use this as an opportunity to educate.  Don’t do what’s easy – step up, show up, and do what works.

What you should know…

Let’s go back to cancer.  Here are a few basic need-to-knows about cancer:  first, it’s NEVER fine.  It is insidious, and a cancer diagnosis stays with you for life.  Yes, you celebrate milestones of getting past it at its various stages, but the fear of recurrence is always with you; every second of every minute of every day.  AND the physical, mental, and emotional effects of pumping actual poison (or radiation or cutting up your organs) into your body to eradicate the cancer NEVER go away.  They say 1 year of chemotherapy ages you 10 years.  Well, folks, I can personally attest to that factoid.

To review my examples, what should these people have said?  About the 30th chemotherapy session:  “I know they never get easier.  I am thinking of you today.”  About the clear scan:  “That’s great news!  Hope it continues to go well!”  About rehabilitating my life:  “I can’t even imagine (or if you are a fellow survivor), I understand.  Hope every day you feel stronger!”

More people are battling cancer and thankfully more people are surviving cancer than ever before.  Cancer totally sucks but coming together to seek a deeper understanding of this disease and how we can best know how to help those in greatest need can surely bring us all “closer to fine.”

Filed Under: My Journey

Website 2.0 – Why It’s So Important to Me

January 27, 2018 by Stacy Hurt

The Road Well Traveled

Self-Awareness is an underestimated skill.  I know what I’m not, but the journey to figure out what I am has been a rather complex one.  As a matter of fact, I’m still not quite sure.  But at age 47, I think I’m getting closer.

First, I was a precocious, inquisitive child, who wanted to be the first woman President of the United States.  Then I got kind of lost in my 20’s, wanted to host my own talk show, and stayed on track enough to attain two Master’s degrees.  Then I discovered I was pretty good at sales.  And then I got punched in the face.  And then I found out I was pretty good at training.  And then I got punched in the face again.  And punched yet a third time… And now I’m the star of my own, “where are they now?”

Who is “Stacy”?  I love people, I have a few letters after my name, and I can get up after getting knocked down.  I don’t think any of this is going to make me rich.  I wanted to get rich in my “lost 20’s.”  Now I just want to survive, learn how to cook, raise my family, and make a difference.

So what really happened and where am I going with this?  In a nutshell, I worked in sales, training, and healthcare.  Then my younger son was diagnosed with profound disabilities and special needs to the point that he will never walk or talk and requires total one-on-one care for the rest of his life.  Then I was diagnosed with Stage IV colorectal cancer that will entail maintenance treatment for the rest of my life.  Then my mom was diagnosed with unexplainable total hearing loss that required a cochlear implant and adaptations to her lifestyle to give her some ability to communicate.

But I Get Up Again!

The end, right?  On the contrary, that’s just the beginning!  Just to review:  gift of gab, lots of smarts, lots of experience, lots of adversity.  Do I get bitter and curse out the universe?  Do I curl up into the fetal position, grow my hair long, and become a recluse?  Well, no.  I’m a person who LOVES people – I used to enjoy just talking to them, but now I more enjoy listening to them and helping them.  And I’m feisty, which really means that I’m not happy unless I’m pushing the envelope in some fashion.  I’m a disruptor.  Since the world of cancer and disabilities needs more inclusion and acceptance, I’ve chosen that particular area to focus my still yet undeterred energy.

Introducing https://stacyhurt.wpengine.com –  a way for me to take all of this and help the world, either through advocacy, speaking, or consulting.  AND, better yet, a way for my supporters to help the world through showcasing efforts of humanitarianism with the hashtag #DoingAwareness (read more about that here).

A couple of other important things you should know about me are that I’m super positive, super determined, and I love to make people laugh.  You’d better believe that those qualities have helped me beat down Stage IV colorectal cancer (when I had tumors in 27 places…), helped me raise Emmett to do more than the doctors ever thought he would, and help my mom not be confined by deafness.  Three awful things happened to me without any warning or reason.  (Isn’t there some rule of three somewhere?)  We’re putting all of that behind us, moving forward, and encouraging others to do the same!

So you see, it’s so much more than a website to me.  It’s a lifetime of twists and turns that have defined my mission.  Tons of people have stood beside me and cheered for me along my road of fighting cancer. They all said, “you are inspiring more people than you’ll ever know.”  This just takes that to a whole new level!  So I have YOU to thank for this.  YOU are the driving force behind my endeavors!  Come celebrate life with me on https://stacyhurt.wpengine.com, and share it with someone who needs a boost.  And THANK YOU for helping me to figure out what I want to be while I’m still growing up!

Filed Under: Life Lessons, My Journey

A Magical March for Colon Cancer Awareness Month!

April 20, 2016 by Stacy Hurt

Since I can’t steal “March Madness,” I thought I’d go with this!  Plus, there certainly was a lot of magic, and unlike my whole diagnosis and treatment, this is an experience that I WANT to relive… over and over!  So, I excitedly wanted to tell you about my amazing March (and we may just spill into April by a few days…).

First, was the official news that I was NED (no evidence of disease) on March 1st, the first day of Colon Cancer Awareness Month.  I’ve received so many signs along my journey, and this was certainly one of them.  We met with the same lung surgeon and the radiation oncologist who declared that my radiation treatments last October produced “satisfactory results” (surgeon speak) and now, it was determined I did not require additional radiation at this time.  That report, coupled with my first clear scan at the end of January declared me NED.  Since Stage IV colon cancer has one of the highest recurrence rates, the doctors don’t talk about “remission” or “cure” for at least 5 years, which means I keep going for chemo every 3 weeks indefinitely.  They call it “maintenance chemo” to keep the cancer away (that’s the goal).  Maybe it’s a lower dose, but I still feel sick, fatigued, and generally cruddy.  And I’m still on my 48 hour poison pump, which is a pain.  Many survivors have been NED and then suffer a recurrence somewhere, so I have to stay hypervigilant and on top of this shit.  Next scan is at the end of May.  Feel free to start the focused prayers/positive vibes now…

March 2nd was my bigger than life (literally) appearance on the Nasdaq screen in Times Square to “Join Genentech in the fight against colon cancer.”  Thank God it only rolled occasionally and for one day.  No one should be subjected to “Big Stace” quite that big.  But what a trip!  Every time I watch Shark Tank and see Kevin O’Leary standing in front of that screen at the opening credits, I always shout, “that was me!!”  Just getting the word out… in a BIG way!

Times Square - Genetech

March 4th was my next great day – National “Dress in Blue” Day for a future free of Colon Cancer.  A couple of friends of mine (Lynne Yater and Alissa McLellan) organized a fundraiser for the Colon Cancer Alliance in my honor, which was hosted St. Clair Fitness Center.  The girls ran a few pretty intense exercise and body pump classes – all I could do was witness in sheer awe… I took part in the brunch!  LOL!  I got to tell my story to a gym full of people who appreciate taking charge of one’s health through sweat and hard work!  I admire these folks!  One highlight was meeting Arthur Moats (Pittsburgh Steeler), who was there to work out.  And he listened to my story!  What an honor!  Now I have heard of Arthur Moats but when I was introduced, I just wasn’t putting it together (FAIL!), so I looked like somewhat of an idiot.  Meanwhile, Arthur is one the most sincere, down to earth, gracious individuals that I have ever met.  So respectful – so humble.  Wow!  It was really a pleasure to make his acquaintance.  THANK YOU Lynne & Alissa for a GREAT morning filled with positivity and lots of oxygen flowing in that room!

I hopped the T (I know… hard to believe that a big celebrity like me didn’t have a car service… scoff, scoff) downtown the same day to speak at the UPMC Integrative Oncology Breathing Room event at the Fairmont Hotel for my buddy, visionary oncologist, Dr. Lanie Francis.  Again, I told my story (backed up by my UPMC Medical Mondays video) to a room full of supportive folks who believe in the power of touch, movement, nutrition, and mindfulness to augment effectiveness and offset side effects of traditional chemotherapy.  This is my 2nd year participating in this event that raises money to provide services such as yoga, reiki, massage, and acupuncture to patients who cannot afford them.  Until we can get the insurances to wake up and reimburse for these treatments, UPMC continues to rely on outside support and is constructing a Wellness Suite at Hillman Cancer Center to accommodate a space for providers and patients.  It is a “labor of love”, and I am proud to be a part of it.

[Breathing Room Images Credit: Kylie Kristine Photo]

Next up – March 16th: partnering with Genentech for a Satellite Media Tour.  So what is a Satellite Media Tour, you ask?  Good question!  My treating oncologist, Dr. Vincent Reyes, and I sat in a studio in downtown Pittsburgh (after a heavy makeup application – for me, not Dr. Reyes) while different radio and television stations called in back to back for us to speak live or taped about the importance of screening for colon cancer.  I told my story and Dr. Reyes was the resident expert to speak about incidence and treatment options. It was a loooong day being that “on”, but we had so much fun!  Dr. Reyes and I both love the camera, so we took it super seriously, but were just able to be ourselves, which made it super comfortable.  We joked that we need a road show, because our relationship really showed through, which was what I wanted; as well as to impress my motto:  “if it can happen to me, a total healthy rule follower, then it can happen to anyone!  DON’T IGNORE SYMPTOMS!”

[What You Need to Know About Colon Cancer from NewsWatch Television on Vimeo.]

Other than that, I wrote an article for Everyday Health, was interviewed for another article in Dr. Oz’s magazine, managed to fit in 2 chemo weeks and celebrated a blessed, happy Easter!  (He is Risen!  Alleluia!).  Well, I am exhausted just writing this, and I’m in a treatment week yet again, so I am heading off to rest.  Thank you for reading this and for supporting my mission and passionate purpose.  I really mean it when I say, I love you!

Peace out,

Stacy

Filed Under: Integrative Oncology, My Journey Tagged With: Genentech, UPMC

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Chief Patient Officer @Parexel 🫶 Cancer survivor, Rare disease mom/caregiver, Advocate for the unseen/unheard in healthcare 📣 Opinions are my own

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charise_lee Meidas_Charise Lee @charise_lee ·
4 Jun

No emotion just facts and undeniable truth‼️ Exactly this. The glorification of wealthy people and the excuse of their evilness‼️

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parexel Parexel @parexel ·
29 May

Parexel today announced the company will present five posters highlighting key research at the 2025 @ASCO Annual Meeting May 30-June 3 in Chicago. Newly appointed Chief Medical Officer, Dr. Charlotte Moser, will attend along with the company’s expert Oncology and Hematology team.

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stacy_hurt Stacy Hurt (she/her)🌻 @stacy_hurt ·
28 Apr

This guy is THE BEST! Congratulations Jerry!

PGA TOUR Champions @ChampionsTour

Win No. 13 for Jerry Kelly 🏆

The 58-year-old claims his first victory of the year @MEClassicGolf!

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stacy_hurt Stacy Hurt (she/her)🌻 @stacy_hurt ·
18 Apr

I’m fortunate to do work that I love, that makes a difference, and for a company that values me 💗 #dreamjob

Parexel @Parexel

Transforming clinical research from the inside out. Meet @stacy_hurt, our trailblazing Chief Patient Officer. As a cancer survivor, caregiver, and healthcare executive, Stacy brings a unique 360-degree perspective to our work. Explore her story:

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Important Note

Opinions expressed here are my own and do not represent the views of my employer, nor should be construed as medical advice.  Please consult a licensed, trusted health care professional for any/all treatment decisions.

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