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Cancer Warriors
480 members • Free
47 contributions to Cancer Warriors
6d •
Methylene Blue
Does anyone here have any experience with this? I just purchased it and a 660nm red light.
1 like • 5d
Here is what GROK indicates. Do your own Grok search to see the basis for Grok's answer. I have not read any of the yet. To calculate the energy of a single photon with wavelength λ = 660 nm: Formula Photon energy E=hcλE = \frac{hc}{\lambda}E=λhc, where - hhh = Planck's constant = 6.626 × 10⁻³⁴ J s - ccc = speed of light = 3.00 × 10⁸ m/s - λ\lambdaλ must be in meters It’s usually most convenient to express the answer in electronvolts (eV). Step-by-step calculation 1. Convert wavelength to meters: λ = 660 nm = 660 × 10⁻⁹ m = 6.60 × 10⁻⁷ m 2. Use the standard conversion formula for photon energy in eV: E(eV)=1240λ(nm) E \text{(eV)} = \frac{1240}{\lambda \text{(nm)}} E(eV)=λ(nm)1240 3. Plug in the value: E=1240660≈1.8788 eV E = \frac{1240}{660} \approx 1.8788 \text{ eV} E=6601240≈1.8788 eV Final answer The energy of a 660 nm photon is ≈ 1.88 eV (typically rounded to two decimal places for visible/near-IR light). For more precision: 1.879 eV). (This is a deep red photon—common in red laser pointers.) 1.2s Fast Is this 1.88eV energy adequate to break chemical bonds in human tissue? Yes, 1.88 eV (660 nm deep-red light) is more than enough energy to break many common chemical bonds in human tissue. Here are the typical bond dissociation energies for bonds found in biological molecules (in eV per bond): Bond typeApproximate energy (eV)Can 1.88 eV break it?O–H (in water, alcohols)4.4–4.8NoC–H4.0–4.3NoC–C3.6NoC=C (alkene)~4.9NoC–O (single)2.5–3.6Sometimes / marginalO–O (in peroxides)1.5–2.2.2YesS–S (disulfide bridges in proteins)2.2–2.7Marginal / possibleC–S~2.7MarginalC–Cl, C–Br, C–I (if present)2.5–3.4SometimesPeroxide linkages~1.5–2.1Yes What 660 nm light actually does in tissue - By itself, 660 nm photons do NOT directly break most normal biological bonds (C–C, C–H, O–H, etc.) because those bonds require UV light (3–5 eV, i.e. < ~400 nm). - However, 1.88 eV is sufficient to break weaker bonds such as: Peroxide (–O–O–) bonds Some disulfide (–S–S–) bonds (especially if strained or sensitised) Certain carbon–heteroatom bonds in photosensitisers
0 likes • 5d
Grok answers this way regarding methylene blue for anti-cancer. I have not read the studies yet, but it seems that clinical trials have demonstrated a correlation between methylene blue and improve cancer outcomes only in basal cell carcinoma, a cancer type that I have had hundreds of removed, including 7 MOHs surgeries, until I discovered the hard way that avoiding all seeds , plants, and their oils and eating a high animal saturated fat diet greatly reduced my basal cell carcinoma rate. There is a 1966 scholarly article which reported this effect in hairless mice. Yes, methylene blue (MB) has been demonstrated to exhibit anticancer effects in preclinical studies (in vitro and in vivo models) and early clinical trials, primarily through photodynamic therapy (PDT)—where MB acts as a photosensitizer activated by red light (e.g., 630–680 nm) to generate reactive oxygen species (ROS) that selectively kill cancer cells. It has also shown promise in metabolic therapy by disrupting cancer cell energy production (e.g., shifting metabolism to make tumors more vulnerable to other treatments) and as an adjunct in chemotherapy or pain management during cancer care. However, MB is not a standard or FDA-approved standalone cancer treatment; its use is experimental, and large-scale human trials are ongoing or needed to confirm efficacy and safety across cancer types. Key mechanisms include: - PDT-mediated cytotoxicity: Light-activated MB produces singlet oxygen and ROS, inducing apoptosis (programmed cell death), necrosis, or autophagy in cancer cells while sparing healthy ones due to selective uptake. - Metabolic interference: MB inhibits mitochondrial function in cancer cells, reducing proliferation and enhancing chemotherapy sensitivity. - Anti-proliferative effects: Inhibits tumor growth, invasion (e.g., via downregulation of matrix metalloproteinases), and metastasis in models. Evidence from Preclinical Studies A 2023 systematic review of 10 preclinical studies (across colorectal, breast, melanoma, and other cancers) found MB-PDT reduced tumor sizes in 7 studies, with doses of 0.04–24.12 mg/kg. Nanotechnology (e.g., MB-loaded nanoparticles) enhanced efficacy by improving delivery and ROS production. Other findings:
5d •
A new anti-cancer immune therapy, Immunity Bio ANKTIVA
ImmunityBio 2025 Aug 26 press release, on finance.yahoo.com, https://finance.yahoo.com/news/initial-data-shows_100_disease-123000153.html, an intital study is claimed to have demonstrated that 5 out of 5 patients with recurrent glioblastoma (glioblastoma growing after the standard protocol) demonstrated "100% disease control" (cancer volume not increasing) with 2 of the 5 "in near complete response". Glioblastoma is a difficult case, being inside the blood brain barrier. They indicate that is may prove to be effective on most or many cancer types.
6d •
Mother of my children has passed on due to glioblastoma brain cancer
1960: polio vaccine pulled for causing cancer via SV40. 1965: the first scholarly articles were published on gain of function of SARSCOV2. SARS bird flues repeatedly shut the world down over the decades. 2020 Jan 28 I shared a scholarly article proving that the SARSCOV2 virus was human made. All scholarly articles were censored. When the jab was pushed on us all by our employers and college administrators I discussed everything in details, and indicated that no family member get jabbed, saying health comes first, we would survive loss of employment and college. I discussed SV40 in jab. Secretly the mother of my children got herself, our children, and her parents jabbed. The health of our entire family except me was wrecked. She accepted 3 boosters as required by her hospital employer. Intuitive Surgical ended my employment. She got a leg-length blood clot. She got glioblastoma. I sent her scholarly articles and discussed repeatedly and at length that the "evidence based standard of care Stupp Protocol" was ineffective, expensive, and was a death sentence. I studied, recommending the standard surgery, declining the brain irradiation, minimal corticosteroids, the Thomas Seyfried Press Pulse Protocol, high fat beef eggs hard cheese no carbs keto diet, 6-diazo 5-oxo L-Norluecine, fenbendazole, mebendazole, ivermectin, hyperbaric oxygen, intravenous vitamin C, ECGC, laetrile, Apigenin, leave of absence, possibly an electric field generator, provided spreadsheets to track her Press Pulse Protocol. I am a scientist. She declined all of this other than the Stupp protocol, accepting surgery, irradiation, and chemotherapy that I agree with Seyfried appears to work by making patients so sick to be unable to eat which forces into ketosis. . The glioblastoma slowly at first then exponentially quickly took her capabilities away. She at 62 passed away surrounded by her loving family. ImmunityBio ANKTIVA came too late for the mother of my children, but for those with glioblastoma and most cancer types search for the ImmunityBio 2025 Aug 26 press release, on finance.yahoo.com, https://finance.yahoo.com/news/initial-data-shows_100_disease-123000153.html, where an intital study is claimed to have demonstrated that 5 out of 5 patients with recurrent glioblastoma (glioblastoma growing after the standard protocol) demonstrated "100% disease control" (cancer volume not increasing) with 2 of the 5 "in near complete response". MichaelEdwardWright@gmail.com
1 like • 5d
@Bernardo Henriques Thank you Bernardo
1 like • 5d
@Lemon P Thank you, Lemon P
11d •
resources, physician or university, hospital, clinic
My cancer was initially diagnosed between 1 & 2 stages for which I supplemented. I am back trying to piece together an oncologist and location or system for care. I have traditionally inadequate health insurance and need help navigating what works for a throat tumor, mantle cell lymphoma diagnosis. I unsuccessfully tried to schedule tumor reduction surgery followed by carbon ion therapy. I welcome the sharing of experiences.
1 like • 6d
Ivermectin has been repeatedly reported to be effective especially on throat cancer including late stage. Search for mail order sources. I have posts listing sources. I use Petmectin from Virex Health.
Jan 13 •
A Post I Made in Other Community
I wanted to share a post I made in other community, as I think it's also relevant and useful here: I've attached a comprehensive questionnaire for Tracking and Documenting Experiences with Metabolic Therapy. I developed it together with a help from my friend. Actually he did all the work 🙂 Please note that I am not a research expert, so this is the extent of my contribution. For further technical discussions on refining the questionnaire to achieve optimal results, I recommend consulting a research expert. Here's a comprehensive questionnaire designed for online platforms like SurveyMonkey or Typeform, focusing on experiences with metabolic therapy. Questionnaire Title: Tracking and Documenting Experiences with Metabolic Therapy Introduction (Displayed at the beginning of the survey): Thank you for participating in this important research initiative. This questionnaire aims to track and document the experiences of individuals using metabolic therapy and related approaches for cancer issues. Your contributions will help build a valuable dataset for long-term analysis and potentially establish large national cohorts. Please be assured that all responses are anonymous, and the survey will remain open indefinitely, allowing you to contribute at your convenience. Section 1: Background Information - 1. What is your primary cancer diagnosis? (Open text field) - 2. How long have you been dealing with this? (Dropdown: Less than 1 year, 1-3 years, 3-5 years, 5-10 years, 10+ years) - 3. Have you been formally diagnosed by an Oncologist? (Multiple Choice: Yes, No, Unsure) - 4. If yes, what was the full diagnosis? (Open text field) - 5. What other health conditions, if any, do you have? (Open text field) Section 2: Metabolic Therapy and Related Approaches - 6. Have you used Metabolic therapy? (Multiple Choice: Yes, No) (If Yes to Q6): 6a. How long have you been using Metabolic therapy? (Dropdown: Less than 1 month, 1-3 months, 3-6 months, 6-12 months, 1+ year) 6b. What specific components of Metabolic therapy have you used? (Checkboxes: Please select all that apply. Include options based on the specific components of Metabolic therapy. Example: Press Pulse Protocol, Specific exercises, specific repurposed drugs and supplements, specific mindset techniques, etc. Add an "Other (please specify)" option with an open text field.) 6c. Where did you learn about Metabolic therapy? (Multiple Choice: internet, online community, friends and family, Book/Publication, Other) - 7. Have you used the Press Pulse protocol? (Multiple Choice: Yes, No) (If Yes to Q7): 7a. How long have you been using the Press Pulse protocol? (Dropdown: Less than 1 month, 1-3 months, 3-6 months, 6-12 months, 1+ year) 7b. What specific aspects of the Press Pulse protocol have you implemented? (Checkboxes: List key aspects of the protocol. Example: Press Protocol: 1. Diet: Ketogenic diet, Keto carnivore diet, Paleolithic Ketogenic Diet, etc. 2. Exercise: Aerobic, Zone 2 aerobic, resistant training, HIIT, etc. 3. Supplement: Curcumin, EGCG, Vit D3 and K2, Melatonin, Lugol’s iodine, Milk thistle, MCT oil, Ginger, etc. Pulse Protocol: 1. Repurposed drugs: Ivermectin, Mebendazole, Fenbendazole, DON, etc. 2. Others: HBOT, Hydrogenated gas and water, sauna, etc. Add an "Other (please specify)" option with an open text field.)
1 like • Jan 14
Thank you, @Fitch T
1-10 of 47
@michael-wright-8925
Surrogate for a loved one with glioblastoma. Scientist. Seeking Pulse Therapy medical service providers as close to Seattle, WA, USA as possible.
Active 15h ago
Joined Dec 2, 2024
INTJ
Seattle, WA, USA
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