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Cancer Warriors ❤️
This group exists so no one has to walk this path alone. Share as much or as little as you feel comfortable: - Your diagnosis or a loved one’s journey - What brought you here - Questions you’re exploring - Therapies or strategies you’re researching - Or even a photo — faces help turn stories into connection Every share matters. It helps others feel less isolated and strengthens the collective wisdom of the group. 📌 Post Categories — How to Share To keep the community organised and easy to navigate, please choose the category that best fits your posts: 📢 Announcements: Official updates from the Admin team. 👋 Introductions: Say hello and share as much (or as little) as you’re comfortable with about your journey. ❓Questions: Questions and thoughtful answers from the community. 💬 General Discussion: Open conversation on cancer, healing, mindset, and community-related topics. 💡Research & Protocols: Research, studies, resources, protocols, and learning materials. 📝 Journeys & Experiences: Personal stories, protocols being explored, progress updates and testimonials. ❤️ Community Lounge: Anything that doesn’t clearly fit another category. If you’re unsure, don’t worry — just choose your best guess. The goal is sharing, learning, and supporting each other, not perfection.
Cancer Warriors ❤️
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MRI results - near complete response
Hi fellow warriors! ✨ Just a quick update on my journey. I took an integrative approach to my last protocol, combining radiation with fasting, HBOT, repurposed drugs, RLT, and a GKI-friendly meals. I’m happy to share that I’ve achieved a “near complete” treatment response. This result surprised my oncology team, especially since I opted out of standard “Total Neoadjuvant Therapy” (avoiding Oxaliplatin). Because there’s still some scar tissue and inflammation, I’ll need a sigmoidoscopy to see how much of Shrimpy Boy is actually left (if any). My radiation oncologist and I are hoping it’s actually inflammation of surrounding tissues. 🤞 Now I’m moving into a “watch and wait” phase, supported by my oncologist’s knowledge that radiation’s impact can continue to work on tumour cells for months, especially when supported by metabolic therapy. I’m staying patient and vigilant, hoping that this is either a full response or one that will become “complete” very soon. Part of me just wants to fast the shit out anything left, but with knowledge that autophagy can also be weaponised by cancer cells, I’ve decided against this. Best of all I’ve avoided the “near certain” side effects of pelvic radiation—no burns, no bowel issues, and my fertility is intact. I know this might not last forever and I’d be delusionally optimistic to not expect late-onset side side effects. I’m not sure how much longer I’ll stay away from antioxidants due to the “antioxidant paradox”, which ultimately led to my decision to pause some of my supplements and not take Vitamins C, A, E, and CoQ10 during the seven weeks of radiation. Because they act as free-radical scavengers, reintroducing them can risk lowering ROS within the cancer cells, inadvertently shielding Shrimpy Boy from continuous DNA damage over time. I acknowledge that not everyone agrees with pausing antioxidants and that the data remains highly conflicting. Ultimately, this was a decision made strictly for my own peace of mind, rather than an assertion of personal expertise (and is NOT medical advice).
MRI results - near complete response
high dose pulse vitamin K2 is associated with fighting cancer
This video summarizes some study findings. The video states that the highest dose per capsule is 1.8 mg. He seems to be unaware that vitamin K2 is available in bulk at vastly lower cost than anything that he recommends, see the below link to the Bulk Supplement K2. I take 2 mg K2 twice a day by adding the Bulk Supplement powder in my glasses of water., and I do not have cancer as far as I know. https://www.amazon.com/dp/B087L367W8?ref_=ppx_hzsearch_conn_dt_b_fed_asin_title_1 https://www.youtube.com/watch?v=Gxrew8iFaY4
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Find Other Warriors With Your Cancer Type
To help everyone connect more easily with others on a similar journey, please comment below with: 1. Your Cancer Type (e.g., Cervical Adenocarcinoma, Triple-Negative Breast Cancer, Glioblastoma, etc.) 2. (Optional) Stage/Grade (e.g., Stage 3, Grade 2). Example: “My mum: Cervical Adenocarcinoma, Stage 4.” This way, members can find and connect with others who truly understand the specifics of their situation. Feel free to browse the comments and reach out to those you relate to!
🔥 Dr Robert Yoho & Prof. William Supple
Dr Robert Yoho interviews Prof. William Supple re his new book. https://fenbendazole.substack.com/about https://fenbendazole.substack.com/p/cancer-is-a-parasite-kill-it-with?utm_source=publication-search https://fenbendazole.substack.com/archive The video is re Fenben, not Vit D3, but D3 is mentioned in the first few mins. Prof. Supple’s D3 book will be published in June 2026 *The Prof’s D3 is 110 NG. *The Dr’s D3 is 130 NG. Those👆are USA lab numbers. In the UK, labs give D3 results as NMOL, not NG. To convert NG to NMOL, multiply 1 NG x 2.5 NMOL Therefore... The Prof's D3 of 110 NG in the USA = 275 NMOL in the UK. The Dr's D3 of 130 NG in the USA = 325 NMOL in the UK. I’ve enc. another - audio - interview w/ Prof. William Supple, for those who want to hear it. https://m.youtube.com/watch?v=UGhttMRJRyg&pp=0gcJCZoBo7VqN5tD https://m.youtube.com/watch?v=7SYtShhFQds
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Cancer Warriors
skool.com/cancerwarriors
Cancer support group for patients & caregivers exploring chemotherapy, immunotherapy, metabolic therapy, nutrition and integrative oncology
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