All, I have about 6 weeks of unused Lenvima 10mg pills. I was taking this with Keytruda for my endometrial cancer. My cancer became resistant to Lenvina and my oncologist would like me to stop taking the medicine. The manufacturer and pharmacy will not let me return the unused packages. I know this medicine is very expensive. Please let me know if anyone would like it. I would rather give it away than have the medicine destroyed.

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!

Hi Warriors ❤️ It’s been quite a while since I’ve posted, and I wanted to check in with everyone. As many of you know, I’ve been going through an incredibly difficult time following the loss of my mum. She was my best friend and the inspiration behind this community. I’ve needed some time to process everything and focus on my family. There are still many unanswered questions surrounding her final hospital admission. I’ve requested access to her medical records and am currently waiting for them. Unfortunately, progress has been slow, and it feels as though things became more defensive once concerns about potential clinical negligence were raised. At the moment, I’m trying to understand exactly what happened. There are several aspects of her care that I still struggle to reconcile, including concerns about severe COVID pneumonitis that appeared to be dismissed, decisions made during her admission, and the rapid decline that followed. My hope is that obtaining the records will provide some clarity and answers. Sometimes I find myself wondering “what if?” and wishing we had been given more time. Everything happened so quickly, and we never even had the opportunity to try the new protocol from Astron Health that we had been exploring. Since losing my mum, I’ve found myself replaying everything over and over in my head. Wondering if there was something else I could have tried, another question I could have asked, another avenue I could have explored. But if I’m completely honest, my biggest regret isn’t a treatment, a protocol, or a therapy that we didn’t try. My biggest regret is not showing her more love. I was so focused on finding answers. So focused on finding a cure so that she could live. I spent countless hours researching, reading studies, analysing scans, tracking symptoms, and learning everything I possibly could. Every day felt like a race against time. I was constantly thinking about the next step, the next blood test, the next scan, the next treatment, the next possibility.

I had a checkup with my oncologist yesterday after an MRI and CT scan and want to give people some hope. There has been no progression, no spread of the disease. The MRI on my brain was clear and not spread throughout the rest of my body. The big news she gave me is that the tumor in my lung is no longer there and no sign of it in my lymph nodes, the scan was completely clear. The middle lobe of my right lung has collapsed and all that is left is scar tissue. For all intents and purposes the cancer is no longer there. I am now in the position that I have to continue keeping my body in a state that keeps it unfit for cancer to survive. Never give up!! Over two years in, and this news has me over the moon. I thank this community for the support and information, as it is in large part responsible for my good news.

I recently reached out to Dr. Dominic D’Agostino with a question many of us have asked: Is it more effective to pulse oxidative or cytotoxic therapies on consecutive days (e.g., Mon–Wed) or spaced out (e.g., Mon/Wed/Fri)? Here’s what he shared: “This depends on the type of pulse therapy, cancer type, standard of care, individual response, specific biomarkers, etc. There is little data and it is hard to speculate. We did M/W/F for HBOT in mice for a variety of reasons discussed in our publications. My approach would be to apply other pulse therapies in a way that causes minimal or no side effects. Dosage can be adjusted and individualized as response is observed.” — Dr. Dominic D’Agostino Takeaway: There’s no one-size-fits-all answer. The best pulsing schedule is likely the one that: - Causes minimal or no side effects - Fits within the patient’s overall metabolic protocol - Can be adjusted based on response and biomarkers For example, in a mouse study using a ketogenic diet + HBOT (hyperbaric oxygen therapy), they used a Monday/Wednesday/Friday schedule. This might offer a model worth considering — not because it’s universally best, but because it’s been shown to improve survival in that specific context. As always, keep in mind: - The cancer type and progression matter - Therapies like IV vitamin C have short half-lives (2–3 hours), so timing may influence effectiveness - Cancer cells can adapt — so switching things up periodically might help If you’re pulsing therapies in your own or a loved one’s protocol, consider tracking biomarkers, symptoms, and energy levels. Personalization and flexibility are key.