
Finally, a place where you can speak freely about your real cancer journey—without getting censored, judged, or shut down.
JOIN THE COMMUNITYYou get the diagnosis. The world stops. Then everyone becomes an expert on what you should do.
Your oncologist gives you the “standard of care” playbook—the same protocol they give everyone with your diagnosis. When you ask about alternatives, you get the look. You know the one.
Your family means well, but they panic when you mention anything outside the approved playbook. “Just trust the doctors,” they say, as if questioning treatment options means you’ve lost your mind.
Facebook groups? Forget it. They each push one silver bullet cure and if you mention anything outside of that, an immediate BAN!
Share a PubMed study about metabolic approaches and your post gets deleted. Even asking innocent questions about diet gets you labeled as “dangerous.”
185 Pubmed Studies on how repurposed drugs
Dosage protocols from patients actually in the fight
Meditation and spiritual practices to you stay grounded
Direct links to research that social media platforms shut down
Dr. Thomas Seyfried on metabolic approaches
Roger Rasmussen (author of “Finding Fenbendazole”)
Oncologists willing to speak off the record
Researchers whose work gets suppressed
Private forums to discuss side effects, questions, and opinions that get censored elsewhere.
Monthly Q&As with experts who are in the trenches of the medical freedom movement.
Private forums organized by cancer type
Stories from patients and caretakers who have been where you are
Connect with others fighting the same battle
Exclusive discounts on medications, genetic tests, and supplements
Support that those around you can’t offer
Celebrate wins and ask questions without judgement
The most dangerous part of a cancer diagnosis isn’t the disease itself—it’s the isolation that comes from being told there’s only one “right” way to fight it.
When I was diagnosed with stage III breast cancer in 2022, I discovered something shocking: asking questions about your own treatment makes you “difficult.” Exploring options beyond the standard protocol makes you “dangerous.” And feeling like something’s missing from your care plan makes you “crazy.”
Then I ran into a high school friend who was also battling breast cancer.
We both confessed we weren’t doing well, weren’t feeling heard. As we compared notes, we realized something profound: we weren’t crazy. We were both feeling an intuitive pull to do something different, but we needed to hear each other’s story to find the courage to trust that instinct.
The research exists. The options are real. But the system actively discourages patients from exploring anything beyond the standard playbook.
We needed our own space—a place where asking questions doesn’t get you labeled, where exploring options doesn’t get you banned, where trusting your instincts doesn’t make you “anti-science.”
Cancer Crew exists because sometimes the best protocol is the one that fits YOUR situation.
And you can’t find that protocol if you’re not allowed to talk about it.