Hi Team, I got some fabulous news. PET scan and Natera blood work both says cancer is gone. Plan going forward is to keep getting Jemperli Immunotherapy every 6 weeks for the rest of my life. I am also continuing with Febendazole and Ivermectin,

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

Dr Paul Marik: Modified Citrus Pectin (MCP) binds to a specific protein called Galectin-3. Galectin-3 is expressed on cancer cells and allows them to bind to the endothelium. It allows the cancer cells to get through the endothelium. It allows the cancer cells to clump together, and so it plays a really important role in the metastatic process. There's really good data, particularly in experimental models. If you give MCP, which binds to Galectin 3 you reduce the risk of metastasis. MCP is taken orally. It's safe and has no side effects. EOM -------------------------------------- If so, please share your experience here. Thank you. The video: https://youtu.be/Al_NPY5AiI8?t=2023

Joining this community to feel less alone as we walk through DIPG with our 12-year-old daughter Isla. Please keep her in your prayers. ❤️

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).