Dr Boz tells a story of one of her group members. https://www.youtube.com/live/kpsbaMhUa9k

Dear all, this new classroom is just in the planning stage, let's make it happen! The idea is to create a crowdsourced classroom where members share real-life progress stories, connect with other members, and find renewed hope. What’s a story of progress and success? Any win, big or small. Remission, or just moving forward. Let's start small; we've got some recent success stories. @Jeff Boldrick , @Whitney Khan , can we post yours in the classroom to kick things off? Also recalling @Odette Rocha , @Michelle Love and @Hengameh Bolouri had great stories, if I remember correctly. Can we add yours too? Others with great stories, please share! No, it's not bragging, it's giving hope to others. Moving forward, all admins can add member success stories from the community to the classroom (with permission). How does that sound?

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.

I asked Nhs a couple yrs ago and was told it’s unavailable in UK for renal / kidney cancer. I looked into it again recently & saw that some staff at Royal Free hosp & Royal Marsden hosp are looking into it, but it’ll be unavailable for yrs. Has anyone queried doing it in the UK, even privately, to track renal cancer? If so, any idea which private lab does it and for what fee? Does Exacta360 or another organisation offer it for tracking renal cancer?

Just had my scan result and I’ve managed to shrink my largest met by 5mm from 65mm, a lung met also had a bit shaved off and my pancreas met looks thinner but the same length! What did I do? Well I added in fbz to the protocol 3-4 months before the scan and I added iscador Qu by subcutaneous injections for 4 weeks before the scan. A previous IV mistletoe therapy for an 5 week period gave me stability in the next scan. Mistletoe is an immune system mobiliser If you can do that and have some sauna’s/fevers I think you might get things working better. I’m carrying on with another course of iscador qu and will try and keep it going for 3 months. My oncologist went ape about it but I think it’s having an effect.