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Something big is unfolding here…🌅

Stepping into 2026 with a new BRCA & Beyond logo…and a deeper meaning behind it.

Every part of this symbol was created to reflect what life looks like after diagnosis:
the moment everything changed, the hurdles you’ve crossed (and are still crossing), the grace that carries you, and the light that reminds you there is still so much life ahead.

This community has always been about more than awareness.
It’s about identity, healing, resilience, motherhood, and becoming; even after cancer, genetic testing, preventative surgeries, and the hardest decisions of your life.

Because your life doesn’t end at diagnosis.
It continues.

BRCA & Beyond: Life After Diagnosis
Season 2, Episode 1 is out now — and big things are coming in 2026 🤍

If you’re navigating hereditary cancer risk, genetic mutation, preventative surgery, surveillance, cancer recovery, or learning how to live fully again after life-altering news — this space is for you.

✨ Share it with someone who needs hope today.

_____

#BRCAandBeyond #BRCA #BRCA1 #BRCA2 #Previvor #CancerSurvivor #HereditaryCancer #MastectomyRecovery #Salpingectomy #CancerSupport #HealingJourney #survivor #WomenSupportingWomen #Survivorship taken in New York, New York by @brcaandbeyond
32
7 months ago
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Could creatine do more than support muscle health? 🧬

A new UCLA study found that creatine helped power dendritic cells…important immune cells that activate T cells, in mouse models and human immune cells in the lab.

While the findings are promising, this was a preclinical study. Human clinical trials are still needed before any recommendations can be made.

I love sharing new hereditary cancer, genetic mutation, and cancer research to help keep our community informed.

I’m not a doctor or healthcare professional. This post is for educational purposes only and summarizes research published by UCLA. 

🚨Always talk with your healthcare team before starting any new supplement.

💬 Would you like to see more research breakdowns like this? taken in Florida, USA by @brcaandbeyond
9
21 hours ago
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Some things just end up being worth every single penny.

If you’re preparing for a preventive mastectomy, breast reconstruction, hysterectomy, salpingectomy, or another surgery related to cancer, here’s something I wish more people knew…

Before paying out of pocket, ask questions.

Talk with your surgeon, hospital, physical therapist, and insurance company about what resources may already be available to you. 

Depending on your situation, services like physical therapy, lymphedema therapy, lymphatic drainage massage, and other post-operative recovery services may be covered, partially reimbursed, or even provided through your hospital or cancer center.

You never know what’s available until you ask.

Now I want to hear from you…what’s something you spent money on during your hereditary cancer journey that was worth every penny? 👇

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#fyp #doublemastectomy #previvor #hereditarycancer #geneticmutation taken in Sarasota, Florida by @brcaandbeyond
6
a day ago
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Being high risk shouldn’t mean being low priority.

While establishing care in Florida for my BRCA2 mutation, I was told that because I don’t have an active breast cancer diagnosis and have already had a preventive double mastectomy, I wouldn’t see a breast surgeon…only a nurse, with the first appointment available in April 2027.

As a hereditary cancer previvor, that doesn’t sit right with me.

Risk-reducing surgery doesn’t erase risk. We still deserve specialized follow-up care.

Looks like it’s time to sharpen my pitchfork. 😉

Have you had a similar experience trying to establish care as a high-risk patient or previvor? I’d love to hear your story below.

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#HereditaryCancer #GeneticMutation #fyp #BRCA #Previvor taken in Florida, USA by @brcaandbeyond
29
2 days ago
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What if one conversation about genetic testing could change the course of someone’s life?

In this week’s episode of BRCA & Beyond, I’m joined by Krista Brown, an oncology nurse, breast cancer survivor, and hereditary cancer advocate.

Krista shares her experience living with an ATM gene mutation, being diagnosed with Stage 1A breast cancer, and why she’s so passionate about improving awareness of hereditary cancer, expanding access to genetic testing, and helping others make informed decisions about their health.

We also talk about the realities of inherited cancer risk, advocacy, prevention, finding community, and why education is one of the most powerful tools we have.

Whether you’re living with an ATM, BRCA1, BRCA2, PALB2, CHEK2, Lynch syndrome, or another hereditary cancer gene mutation—or you’re simply wondering if genetic testing is right for you—I hope you’ll give this one a listen.

🎙️ Listen wherever you get your podcasts by searching BRCA & Beyond, or visit brcaandbeyond.com.

I’d love to know what part of Krista’s story resonates with you most. 💛

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#brca #fyp #previvor #genetictesting #cancersurvivor taken in Florida, USA by @brcaandbeyond
24
3 days ago
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One of the hardest parts about living with a hereditary cancer mutation is wondering what the future holds.

The encouraging part? The future isn’t standing still.

Every study, every clinical trial, and every new discovery helps researchers answer questions they couldn’t answer a few years ago. It helps doctors make more informed recommendations, gives families clearer information, and moves us closer to personalized medicine, better genetic testing, earlier cancer screening, and more effective cancer prevention.

Whether you carry a BRCA1, BRCA2, PALB2, ATM, CHEK2, or Lynch syndrome mutation, or another hereditary cancer syndrome, research continues to shape the future of care.

Progress in medicine rarely happens overnight. It’s built one study, one discovery, and one patient at a time.

That’s why I believe it’s worth paying attention…not because every new study will change your care tomorrow, but because today’s research has the potential to become tomorrow’s standard of care.

💗 I’d love to know… What area of hereditary cancer research gives you the most hope?

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#brca #previvor #hereditarycancer #fyp #cancersurvivors taken in New York, New York by @brcaandbeyond
7
4 days ago
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Three days before Christmas, Marisa got the diagnosis no one saw coming. It was colon cancer. She was 37. Healthy. No family history. Then came the stomach pains, the bloating, the blood in her stool — and finally, an answer she never expected.⁠
⁠
Comment DIAGNOSIS and we will DM you Marisa’s full story! ⁠
⁠
#coloncancer #coloncancersymptoms #coloncancerdiagnosis #thepatientstory⁠ by @brcaandbeyond
35
4 days ago
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There are conversations I’ve had more times than I can count since becoming a previvor.

Not because people are trying to be hurtful. Most are simply trying to understand a reality they’ve never had to live.

The truth is, there are no perfect answers when you’re navigating hereditary cancer risk. Every decision comes with uncertainty. Whether you choose preventive surgery, high-risk screening, or you’re still figuring out what feels right, you’re making the best decision you can with the information you have.

One thing I’ve learned is that the people who matter most don’t need to agree with your decisions to respect them.

If this reel felt familiar, I hope it reminds you that you don’t have to carry those conversations alone.

💗 I’d love to hear from you. What’s one question you’re tired of being asked? Or what’s one question you wish more people would ask instead?

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#brca #previvor #hereditarycancer #fyp #cancersurvivors taken in Key West, Florida by @brcaandbeyond
12
5 days ago
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One of the hardest parts of living with a BRCA, CHEK2, PALB2, ATM, Lynch syndrome, or any genetic mutation isn’t always the appointments or surgeries.

Sometimes it’s learning how to keep living while your brain is constantly trying to protect you from what’s next.

When you’ve experienced cancer, are navigating life as a previvor, or are making decisions after genetic testing, your mind naturally wants certainty. It wants to solve tomorrow before tomorrow gets here.

But life doesn’t wait until everything feels safe.

There are still sunsets to watch.
People to hug.
Conversations to have.
Memories to make.

Fear may always have a seat at the table, but it doesn’t have to make every decision.

If this found you on a day when your mind is racing ahead, I hope you’ll come back to this whenever you need the reminder. 💖

Save this for later, and if someone in the hereditary cancer community, a fellow cancer survivor, previvor, or someone living with scanxiety needs to hear it today, send it their way. by @brcaandbeyond
3
6 days ago
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The waiting can feel just as hard as the appointment itself. 🤍

No one really prepares you for the days between the test and the answer.

The refreshing of your patient portal.
The phone calls that make your heart race.
The conversations in your head.
The wondering.
The waiting.

If you’ve ever experienced scanxiety while waiting for biopsy results, pathology results, genetic testing, an MRI, CT scan, mammogram, or colonoscopy, I hope this episode makes you feel seen.

In this week’s episode of BRCA & Beyond, we’re talking about one of the least discussed parts of living with a genetic mutation, hereditary cancer, and life after a cancer diagnosis…the emotional weight of waiting for answers.

If you’re in that space right now, this conversation is for you. 🤍

🎙️ Listen now wherever you get your podcasts. taken in Florida, USA by @brcaandbeyond
6
8 days ago
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People see prevention. They don’t see what it takes to get there.

Being a previvor isn’t just about screening for cancer. It’s about carrying the invisible work that comes with living with a hereditary cancer mutation.

It’s genetic counseling, MRI appointments, mammograms, colonoscopies, surgeries, pathology reports, insurance battles, waiting for results, and making life-changing decisions most people never think about.

Whether you carry BRCA1, BRCA2, Lynch syndrome, CHEK2, PALB2, ATM, TP53, CDH1, or another inherited cancer mutation, prevention isn’t one decision.

It’s a lifetime of informed choices made with hope…that cancer never gets the chance.

If you’re a previvor, I hope this reminds you that the work you do every day matters, even when no one else sees it. 💖 taken in Sarasota, Florida by @brcaandbeyond
10
9 days ago
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I wasn’t prepared for how these photos would make me feel.

This was the first time Steve and I opened the email with my professional Dear Body Project photos. No previews. No sneak peeks. Just our real, unfiltered reaction.

After becoming a colon cancer survivor, discovering I carry the BRCA2 genetic mutation, choosing a double mastectomy, undergoing breast reconstruction, removing my fallopian tubes, and navigating the emotional reality of hereditary cancer, I honestly didn’t know what it would feel like to see these images.

What I didn’t expect was how healing it would be.

Watching Steve’s reactions were my fav. 😂 he had me laughing while I was trying not to cry. His reactions were exactly what I needed in that moment. They reminded me that even after everything my body has been through, he still sees me.🤍

A heartfelt thank you to @brcastrong for making this experience possible and for believing in the healing power of projects like this and @the_dear_body_project .

Thank you, Franny @looksbyfrannyb , for making me feel beautiful. Thank you to Shirley @sbmedia.group for capturing these moments so perfectly, and to Monica @calligraphymiami for the beautiful calligraphy that made every image even more meaningful.

This wasn’t just a photoshoot.

It was a reminder that healing isn’t only physical. 

Sometimes healing is learning to see yourself through a kinder lens. 💖 taken in Florida, USA by @brcaandbeyond
59
10 days ago
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