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720 contributions to Cancer Warriors
📊 GKI Scores 📊
Feel free to use this thread to post and discuss your GKI (Glucose Ketone Index) scores, share insights, and track your progress with others. We are all here to help each other and having a yardstick of what others can achieve is inspirational and can improve the readings of the group as a whole. Let's keep the vibe positive, supportive, and respectful. We're here to uplift each other - join the conversation! We are not all cancer experts (in fact none of us are trained oncologists) so we have to be open to the ideas of others. If you don’t agree PM the OP and get them to change their post if it’s demonstrably wrong.
3 likes • 13d
@Egg Scrambled I hope everything is okay my friend 🙏💫🤲❤️
3 likes • 7d
My dad after 24h fast. OMAD and Keto made a huge difference. He had pre-diabetes and insulin resistance
For my mum — and for this community
I never imagined I would be writing this. My mum passed away, and I don’t yet have the words to describe the emptiness she’s left behind. She wasn’t just my mother — she was my best friend, my anchor, my reason for fighting, and the heart behind everything we built here. This community was created for her. She carried more than most people ever see. She lived with bipolar disorder. She carried childhood trauma. She endured a painful divorce, the loss of both her parents, a cancer diagnosis, the death of Pepper — our family boxer — and the loss of Albert, our family’s closest friend. All of this happened within the last seven years. And yet — she kept going. She walked at least 10,000 steps a day. She swam three times a week. She went to church every Sunday. She worked tirelessly on the house. She quit smoking after her diagnosis. She tried carnivore. She cut out sugar. And most importantly: She kept our family together. She fought. She cared. She loved. Even when depression weighed heavily on her will to live, she chose to fight — not because it was easy, but because she loved us. She fought for us when her mind told her to give up. That is courage. We were hopeful. So hopeful. She had just started the Astron Health protocol — only one week in — and we believed we had time. Previous scans had been relatively reassuring, showing stable, very slow-growing, localised disease in the peritoneum and a coeliac lymph node, with no organ spread. Her CRP was 4 — within the normal range. Then everything changed — fast. She developed sudden, severe gastrointestinal pain, vomiting, and diarrhoea. We rushed to the hospital. A CT scan showed ischemic colitis. A mouth swab also confirmed COVID. She was put on palliative care, given fluids and heparin. Her circulation improved. Lactate came down. Symptoms improved. Objectively, things were getting better. But the narrative never changed. Despite improving vitals, improving markers, and improving symptoms, they continued to insist on bowel necrosis — even when the evidence did not clearly support it. At the same time, her CRP (an inflammation marker) rose rapidly from 4 (normal) just weeks earlier, to 14 on admission, to 150 the following day, and eventually to 455 at its peak. She developed rising oxygen requirements, hypoxia, and what appeared to be a clear systemic inflammatory storm — yet COVID pneumonitis was repeatedly dismissed.
0 likes • Mar 30
@Monika Sullivan 🙏❤️
5 likes • 9d
I came back to this post and reread all your beautiful messages. Thank you all🙏 @Jeff Boldrick @Paulette Asomah @Shanon Small @Wayne Marlowe @M F @Ernest Wheeler III @Bob Smith @Scott Millsap @Manny Malfavon @Gabrielle G @Egg Scrambled @Whitney Khan @Shashish Kamal @Daphne - Kind Healing @Sandra Albert @Christine Michaud @Susan Lewis @Melissa Mantilla @Lemon P @Lisa Drake @Svetlana Soboleva @Lori Chamberlain @Beth Kosten @Richa Gaur @Fitch T @Laura Baranesky @Gwen Johnson @Odette Rocha @Marie H. @Trish Lehman @Mark Ma @Roxana C @Boris Tahmasian @Michelle Bender @Dmitry Vladislavovich @Michael J @Anita Lawrence @Monika Sullivan @Hadriana Oliveira
My Mum’s Final Days: Why I'll Keep Asking Questions ❤️
My dear Warriors, I’ve been wanting to share something deeply personal with you. As many of you know, my mum was the inspiration behind Cancer Warriors. Everything I’ve learned, researched and shared through this community began with my determination to help her fight cancer. Sadly, my beautiful mum passed away on 15 February 2026, following a 14-day admission at York Hospital. My brother and I stayed beside her throughout those 14 days, sleeping next to her bed at the hospital every night. My sisters and stepdad were also there every day, balancing work commitments and looking after our dogs while spending as much time as possible with Mum. We were all there for her, supporting her and each other through the most difficult days of our lives. Together, we witnessed her struggles, her moments of improvement and the difficult decisions being made about her care. During that admission, we became increasingly concerned about aspects of her treatment, monitoring and clinical reassessment. We asked questions. We requested further medical opinions. We challenged decisions when we believed her changing condition warranted reassessment. On 6 February, we invoked Martha’s Rule, an NHS patient-safety initiative that allows patients and families to request an urgent review when they are concerned that deterioration is not being adequately addressed. On 9 February, while my mum was still alive, our family formally escalated our concerns through PALS. We also submitted a written request for a review by a different clinical team. Unfortunately, my mum passed away six days later. We requested her medical records in March 2026, but we’re still awaiting disclosure. We’ve raised a formal NHS complaint, and the hospital has been undertaking a Structured Judgement Case Review. More recently, HM Coroner has begun preliminary enquiries into the circumstances surrounding her death and has requested a detailed chronology of events from us, together with the hospital’s review.
Start Here 👋
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 yourself and your journey. 💬 General Discussion: Cancer-related questions, opinions, discussions, and anything that doesn’t fit another cancer-focused category. 💡Research & Protocols: Research, studies, compounds, therapies, protocols, resources, and educational material. 📝 Journeys & Experiences: Personal stories, treatment experiences, progress updates, lessons learned, and approaches being explored. ❤️ Community Lounge: Non-cancer conversation — everyday life, pets, hobbies, humour, celebrations, and getting to know each other. If you’re unsure, don’t worry — just choose your best guess. The goal is sharing, learning, and supporting each other, not perfection. ✅ Start Here: Explore the Classroom
Start Here 👋
2 likes • Aug 10
@Angele Florisi Hi Angele, welcome to the group. I’m glad you found us. You’ll find a wide range of experiences and opinions here. Many members have significant concerns about conventional chemotherapy and some have chosen not to pursue it, while others have decided to combine conventional treatment with metabolic approaches or have discussed modified or lower-dose chemotherapy with their oncology teams. One concept discussed by Dr. Thomas Seyfried is that chemotherapy may potentially be used more strategically and at lower doses when combined with metabolic strategies such as nutritional ketosis. That is an area of research and discussion, however, rather than something we should present as established clinical guidance. Given that you have a rare subtype of triple-negative breast cancer with high androgen-receptor expression, I would strongly encourage getting the pathology reviewed carefully and seeking opinions from specialists familiar with this particular subtype before making irreversible decisions. Different biological subtypes can behave very differently, and the evidence for chemotherapy, surgery, radiation and other approaches needs to be considered specifically in the context of your tumour. Our group isn’t here to tell anyone to accept or reject chemotherapy, surgery, radiation or any other treatment. The aim is to share research, experiences and metabolic-oncology information so people can ask better questions and make informed decisions together with appropriately qualified clinicians. Please feel free to share more of your pathology and the research you’ve already found. There are some very knowledgeable people here, and hopefully the community can help you identify useful questions and areas to investigate.
2 likes • 12d
@Dana Greene Thanks for sharing that, Dana. Since you mentioned HPV, AHCC may also be something worth reading about. There has been some research looking at AHCC in persistent high-risk HPV, although the evidence is still relatively limited and I’d definitely discuss it with his oncology team before adding anything during cisplatin and radiation. On a personal note, my sister also had HPV and later cleared it while focusing on her overall health and using supportive measures including vitamin D3 and other supplements. Of course, we can’t say which factor was responsible, and HPV can also clear naturally, but it encouraged me to look more closely at the research around immune support and HPV. If you use the search feature here inside the Skool group and search terms such as ‘HPV’, ‘AHCC’, ‘vitamin D’ and ‘head and neck cancer’, you should find quite a bit of previous discussion and information that may be useful. One important point while he’s undergoing cisplatin and radiation: I’d run any supplement or additional therapy past his oncology team or oncology pharmacist first, because some things can interact with treatment or may need specific timing.
Subject: 2026 almost done... Navigating the information maze
I recently went through radiation therapy, and the information shared in this community has been incredibly useful. There is also a massive amount of information available on Facebook. The real question becomes: which groups are worth your time to participate in and follow? It takes a lot of effort to keep up, but it is deeply helpful if you have the time to invest. One major takeaway for me is that there are so many different opinions on the same topics, and there is a place for all of them since the knowledge base is constantly evolving. For example, there are ongoing debates about whether the Keto diet is appropriate for all types of cancer. I learned about Jane McLelland from this community and read her book, which really helped me understand the complexity of the issue. I have also subscribed to newsletters like makisw.substack.com to see different perspectives. Ultimately, the biggest challenge we all face is this: how do we determine what information is actually reliable?
0 likes • 13d
Thanks for your thoughtful feedback. Jane’s book is amazing. You’re right, determining what information is reliable can be challenging, especially when there are so many different opinions and approaches out there. That’s one of the reasons I want this community to be a place where we can share different perspectives, look at the research, ask questions, and learn from each other without pretending there’s always one simple answer. Really appreciate you sharing your experience, Boris 🙏
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Bernardo Henriques
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@bernardohenriques
Cancer Warriors was inspired by my mum. Building metabolictherapy.com so patients, caregivers & families can access research, education and community

Active 2h ago
Joined Aug 2, 2024
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