10 Hard Truths About A Cancer Diagnosis

When you hear the words ‘you have cancer’, lots of things change.  Here are 10 hard truths about a cancer diagnosis.

cancer survivor breast cancer

When you receive a cancer diagnosis, lots of things change. Some changes are slight, some of them are self-reflective, but most of them will straight-up suck.  Whether you’ve received a cancer diagnosis or your spouse has received one and you’re in it for the long haul, it can be overwhelming. And kids. If you have kids, a cancer diagnosis is probably hardest on them as they don’t even have a perspective on adulthood yet. There’s so much to focus on, so many new terms, new acronyms, new concepts. One thing is true: you’ll be out of your depth unless you’re already an oncologist. Hopefully, these tips will help you through your cancer diagnosis.

Ten Hard Truths When Receiving a Cancer Diagnosis

You Think About Your Funeral

Have you ever imagined your funeral?

I have… and I think every cancer survivor has too.  You see it could be a reality for us sooner rather than later.  I’ve thought about colors (no black please),  music; By Your Side – Sade, Here Comes the Sun – The Beatles, Beautiful Boy – John Lennon dedicated to my boys, and Time Of Your Life – Green Day. Oh, and I want everyone to do a little jig as they are leaving to the final song, Last Dance – Donna Summer.  I want people to go home and remember one funny moment we shared, rather than feel sad that we won’t share more memories.

You Will Never Be The Same Again

Soon after my treatment was complete and the doctor visits slowed, I tried to quickly get back into the groove of my old life to put the Big ‘C’ behind me.

Even though I was looking ‘normal’, things were very different. Physically, things I could do without a problem before were now a struggle.  I now tire very easily (which could be a combination of the medication I take daily OR the fact I’m getting old… let’s face it :-) ). I have no chest strength to lift weights, and my ability to do push-ups is non-existent.  The frustration of these challenges is another constant reminder of what a cancer diagnosis has done to you.

cancer sucks
I love a good cancer diagram!

You Will Have ENDLESS Medical Bills & Paperwork

One of the worst side effects of cancer can be the financial worry. Doctors and treatments are expensive and time-consuming, many are not in-network, and you spend hours and hours on the phone with your health-care provider trying to navigate your plan to get treatments and medications covered. Most drugs are covered by insurance if you are fortunate enough to have it, but others are considered experimental and have to be pre-approved.   Navigating this is stressful, upsetting, and the financial obligation can be downright worrying.  Couple that with having to unexpectedly fight for your life, and you quickly want to throw your hands in the air in frustration and anger, having to deal with this in the first place.
Most facilities, hospitals, doctor’s and treatment clinics will work with you to help pay what your insurance doesn’t pay, but you have to work through the frustrating insurance company process first.

You Wonder How Your Family Will Look If You’re Not Around

“I know I have cancer, but I’m not sure if it’s the kind where I’m dead in a month… if it’s the gnarly kind, you’d better not wallow in grief, but marry someone fabulous so that my boys have a mommy.”  These were the exact words I spoke to Hot Hubby as we were driving to get my biopsy results.  And I totally meant them.  I’ve thought about this a lot.

He can have a 6 month grieving period, but after that, I will be counting on friends to pull him out of his shell, tell him to shave, perhaps help him buy some new fashionable clothes, and dare I say it, even encourage him to date (I promise I won’t walk through walls and haunt you if you do this, you have my word).  It’s so weird to even think about, but I honestly would want my boys and Hot Hubby to move on to their next chapter if it somehow didn’t involve me.  Buuuuttt I’m happy and grateful to be here bossing everyone around for as long as I’m given on this planet!

a cancer diagnoses is hard for children
My dream team

Reconstruction Is A Long Road

For the past two years, since my double mastectomy, I’ve been slowly trying to rebuild my body with the help of my rock-star reconstructive surgeon. Rebuilding breasts is not easy, and certainly not the ‘free boob job’ that some well-meaning people told me was the silver lining to cancer (for real, can’t make this up, and for the record, is NOT something you should ever say to someone with a breast cancer diagnosis).
The reality is my new boobs are two fatty mounds that refuse to move even when I run without a bra, and feel neither pain nor pleasure.  They don’t quite look or act like natural breasts, but in clothes, they look normal-ish, I guess.  Then there are the scars… on your breasts, your stomach, legs (if your surgeon needs to borrow tissue to reconstruct). And let’s not forget the itchiness on the scars and the rippling because the skin is so thin on your chest, due to all the tissue and muscle being removed. The scars all over my body from the many surgeries are a constant reminder of the cancer that tried to kill me.

rehab after double mastectomy - breast cancer
I had hours of intense physical therapy to get the range of motion back into my arms, as nerves were cut during surgery

You Will No Longer Have Control Over Your Body And Emotions

I no longer have control over my body and emotions. The chemicals like Tamoxifen that I take on a daily basis are totally running this ship… some days I barely feel them, and other days I don’t even know who this bat-shit-crazy person is. None of this is deliberate. Please don’t take it personally, and please forgive me. I’d love to not take the drugs, but you see, the cruel irony of this is that those same chemicals that sometimes turn me bat-shit-crazy are the same chemicals that are supposed to keep me alive. Cool.

Cancer Treatments Leave Us Susceptible to…a Future Cancer Diagnosis

Doctors have always assumed the benefits outweigh the risks for CT and PET scans, but a single CT scan subjects the human body to between 150 and 1,100 times the radiation of a conventional X-ray, or around a year’s worth of exposure to radiation from both natural and artificial sources in the environment.

Why is this a big deal?

The radiation in that CT scan to help treat cancer can increase your risk of a future cancer. So you find yourself in a bizarre catch-22.  The upside….I’m alive! I will gladly trade the possibility of having a recurrence of cancer at some future point in my life for the privilege of being alive right now.breast cancer diagnosis

Worry and Anxiety Are Gifts That A Cancer Diagnosis Gives You…For the Rest of Your Life

The worry of cancer will never leave you. Even after you’ve removed it. Even after you’ve “beaten” it. Even after 10 years without a recurrence.

After a cancer diagnosis, and you complete all possible treatments, you get as close to your magical ‘rate of recurrence’ number as possible.  This could be 10%, 15% or 50%, and that number is seared into your brain like a tattoo. Each time you have an unusual pain, you instantly worry about the possibility of a recurrence.  Most people will say, “My head hurts”.  We think, what kind of cancer makes your head hurt? Most people might sit with pain for a while and let it pass.  A cancer survivor will sit with it for a while, but eventually go to the doctor or ER because we just can’t take that chance.  If we don’t get it checked and it is something, it might have spread too far.

For many cancer survivors,  worry is the final gift from cancer. The only difference from one person to the next is how well you learn to cope with it.  I try to tell myself I shouldn’t worry about anything until I actually have something to worry about, and admittedly, some days are harder than others. But over time, anxiety gets easier to manage. It just never really goes away; you learn to live with it.

breast cancer double mastectomy

Cancer (and Cancer Diagnosis Treatment) Side Effects Are Permanent

Pretty much all types of cancers leave lasting side effects.  Some of them are temporary, and others remind you of cancer every day.  These side effects range from simple tingling in your fingers or feet, hot flashes, jagged scars, or hormonal moods caused by the various medications that are supposed to keep you alive.  Then there are the side effects that remind us we’re not who we used to be.  We’re not as sharp as we used to be, we forget things, we ask the same questions, and this makes certain parts of our daily life suck.

Anxiety Around Scans and Doctor Appointments

Even the strongest cancer survivors will experience a feeling, a fear, and sometimes an overwhelming anxiety that hits us when we are waiting for the results of a scan or blood test.  You can have all of your emotions in check, with no worries, and then BAM, going in for your routine checkup can open up the floodgates of your worst fears.  Again, a never-ending reminder that you had cancer, and possibly could again.

The treatments may be over, the surgeries may be over, but cancer is never over. Going to regular doctor appointments, it’s always in the back of your mind…is this the day my life changes? What are these pains in my back? When will my scars become less prominent? Why have I had a headache for two days?  Is my bloodwork going to be normal today? These and other questions are on your mind every day.
You might be done with cancer, but cancer is NEVER done with you.

What do you find the most difficult about dealing with cancer in your life?

Share your thoughts in the comments below.

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About the Author

Hi! I’m Samantha

I’m a travel and health writer, marketing consultant, breast cancer survivor, and proud mum to two young men, who are, without question, my greatest achievement.

I share family travel, destination guides, honest reviews, and the realities of life after breast cancer. It’s sometimes lovely, sometimes messy, but always authentic, and told with my dry (and sometimes naughty) British sense of humor.

I’m so glad you’re here.

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The hotel is right on the bay, close to downtown, Coronado, the Gaslamp Quarter, Seaport Village, and Petco Park. If you’re going to a Padres game, the location is honestly perfect. We walked from the hotel, over the pedestrian bridge, and straight to the ballpark.

The newly renovated rooms are lovely and have everything that matters: a comfy bed, great pillows, and a separate sitting area. I’m not the easiest sleeper, but I actually slept here, which is always my true test.

We ate a delish dinner at Hudson & Nash, the hotel’s signature restaurant with bay views, firepits, World Cup games at the bar, fab seafood, and a cioppino loaded with lobster. 🦞🌅☀️

Definitely ask for a table by the firepits if you can.

Hilton San Diego Bayfront is perfect for a couple’s weekend, a family stay, or a Padres getaway. Easy drive, gorgeous location, and no airport stress.
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Back then, it was just a place to share stories and photos from our travels. 🌎

Then life took a wobble. At a routine doctor’s appointment, I was diagnosed with breast cancer.  It was a dark time. My boys were young, and I genuinely didn’t know what the future would hold. During treatment and recovery, I spent a lot of time in bed. So I started writing. I documented everything. The cancer journey. Family life. The places we’d traveled. The memories we’d made. 💕🌸

To be honest, I think part of me was creating a little corner of the internet where our stories, our photos, and the adventures we’d shared together would live….Just in case I didn’t. Twelve years later, I’m still here. (woot woot!) 🙏

The boys are now young men. Social media exploded. The internet changed. And somehow, this little blog grew alongside it. What started as a personal project became a business, a community, and one of the greatest surprises of my life. Today, My Travelling Circus is where I share family travel, destination guides, travel tips, honest reviews, wellness, family stuff, and life after breast cancer.
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Today, three rescued sea lion pups were released back into the ocean after being cared for by an incredible team of people @marinemammalcare 🦭
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Watching them head home is proof that when people come together to help, amazing things can happen.🙏
Welcome back to the wild, little ones.
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Broadway shows, piano bars, late-night drinks rotating the city, and somehow squeezing in actual work. New York really is the city that never sleeps. Let’s do it again! 
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If you’re planning your own trip to NYC, I have everything you need here:
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Our carne asada and Pork Loin Alambre were cooked to our preference right in front of us, and the food was fresh, flavorful, and somehow didn’t feel heavy at all.
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And the cocktails… very cool cocktail menu. We tried the Coco Verano (with Don Fulano Blanco, Cointreau, Fresh Coconut, Pressed Coconut Water, Agave, Lime) and the house fav. Cucumber + Sal (El Tesoro Blanco Tequila, Chareau Aloe Liqueur, Cucumber, Cilantro, Lime and Black Sea Salt). The margaritas were very much flowing at our table.🍋‍🟩
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The whole experience is social, interactive, and feels like sitting around a taco stand with friends while everything’s cooking fresh in front of you… which actually is where the founders took their inspiration 🇲🇽
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Descanso has locations in LA and Costa Mesa and is perfect for birthdays, date nights, girls’ dinners, or taking out-of-town guests who want a fun LA dinner experience. Save room for dessert… or settle into their very impressive tequila bar for an after-dinner drink.🍸

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The theater is staged in-the-round, so the entire undersea world happens all around you, with the characters sometimes only a couple of feet from the audience. The costumes are gorgeous and beautifully designed to bring the underwater world to life. There was even a performer doing aerial acrobatics on an aerial rope above the stage. And of course, you already know the songs…the pure voice of @jennamaewhite as Ariel is Disney magic 🐠🦀
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One of my favorite parts was watching the little girls arrive in their Ariel dresses, beside themselves with excitement, and at the end, the cast came out to meet them and take photos…so lovely 💕
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The Little Mermaid @thenocturnetheatre 
Dates: May 8th – June 14th
Location: 324 North Orange Street, Glendale, CA 91203
Show Length: 2.5 hours (with intermission)
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- Flew into Dubrovnik (Croatia) 
- Dubrovnik to Mostar (Bosnia & Herzegovina)
- Down through Kotor and Budva (Montenegro)
- Over to Shkodër (Albania)
- Back to Dubrovnik (drop boys at the airport)
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- Korčula to Split (Croatia)
- Split to Dubrovnik (Croatia)

We explored coastlines, islands, mountain roads, old towns… so much culture packed into two weeks. I mapped the full route and shared exactly how we did it (what I’d do again vs skip) over on the blog - link in bio if you’re thinking about it.🌍
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https://www.mytravellingcircus.com/2026/04/25/easy-balkans-road-trip-a-one-week-loop-from-dubrovnik/
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Also special shoutout to my @marcellanyc Signe Dress - the pink is even more vibrant in person 
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If you’re in LA be sure to visit their flagship store 
📍 Our Place, Abbot Kinney
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See my full OurPlace product guide here: 
https://shopmy.us/shop/collections/921589
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Comments

  1. Jacqueline Syring
    November 7, 2021

    I love your blog. Just found it so I’m reading through them all from oldest to newest.
    Just finished October 2017 – 10 Hard Truths about a Cancer Diagnosis
    I’m wondering, now that you are 6 years cancer-free, how are you feeling?
    Do you still tire easily?
    Are you still on all the medications?
    How are you feeling physically? Are you still unable to do a push up?
    Do you still feeling tingling in your finger and feet and have hot flashes?
    Mentally, do you still find yourself forgetting things and not as sharp?
    Thanks so much in advance for answering any of the above questions that you have time for. I really appreciate all the information you’ve posted and wish you years and years of cancer-free living.

    1. Samantha
      November 8, 2021

      Hi Jaqueline! Welcome, I’m happy you found me! So… at 6 years cancer free, I wish i could tell you that I am back to ‘normal’… but I’m not I’m afraid. I do tire easily still and even though I’m off tamoxifen now, I do need to take a medication for my bones which seem to constantly hurt. I’m not sure if that’s a side effect of tamoxifen, or old age to be honest, but I guess I feel a bit more weary. However the good news is my upper body strength is back.. i workout, do yoga, push-ups and am able to be mobile.

      The finger and toe tingling have mostly gone, but I do have hot flashes… the tamoxifen pushed me into immediate menopause and that seems to be where I’m at these days. And sadly, I do have ‘chemo’brain’ and have brain fog. I find myself asking my boys the same questions, or forgetting things easily… it’s more of the short term memory. They are patient and will tell me that I just asked them that, but it’s pretty frustrating.

      However, on the whole, i feel great, happy to be alive and am able to do most things every day. I’m closely monitored by my team of doctors and am just trying to soak in each and every day!

      XXXXX

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  • Jacqueline Syring

    I love your blog. Just found it so I’m reading through them all from oldest to newest.
    Just finished October 2017 – 10 Hard Truths about a Cancer Diagnosis
    I’m wondering, now that you are 6 years cancer-free, how are you feeling?
    Do you still tire easily?
    Are you still on all the medications?
    How are you feeling physically? Are you still unable to do a push up?
    Do you still feeling tingling in your finger and feet and have hot flashes?
    Mentally, do you still find yourself forgetting things and not as sharp?
    Thanks so much in advance for answering any of the above questions that you have time for. I really appreciate all the information you’ve posted and wish you years and years of cancer-free living.

    • Hi Jaqueline! Welcome, I’m happy you found me! So… at 6 years cancer free, I wish i could tell you that I am back to ‘normal’… but I’m not I’m afraid. I do tire easily still and even though I’m off tamoxifen now, I do need to take a medication for my bones which seem to constantly hurt. I’m not sure if that’s a side effect of tamoxifen, or old age to be honest, but I guess I feel a bit more weary. However the good news is my upper body strength is back.. i workout, do yoga, push-ups and am able to be mobile.

      The finger and toe tingling have mostly gone, but I do have hot flashes… the tamoxifen pushed me into immediate menopause and that seems to be where I’m at these days. And sadly, I do have ‘chemo’brain’ and have brain fog. I find myself asking my boys the same questions, or forgetting things easily… it’s more of the short term memory. They are patient and will tell me that I just asked them that, but it’s pretty frustrating.

      However, on the whole, i feel great, happy to be alive and am able to do most things every day. I’m closely monitored by my team of doctors and am just trying to soak in each and every day!

      XXXXX

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