This information is invaluable. I bought a box each of Petmectin & Petdazole just to keep in case I know anyone who needs it. I might keep buying more when I can afford it and keep a little stash for the family.
I'm in Australia and it took about a month to arrive.
This information is invaluable. I bought a box each of Petmectin & Petdazole just to keep in case I know anyone who needs it. I might keep buying more when I can afford it and keep a little stash for the family.
I'm in Australia and it took about a month to arrive.
I hope you never have to offer this to someone with cancer, but if you do, don’t be surprised if the person doesn’t even engage in a discussion about it. I gave this info on these parasitical drugs to our friend who pretty much wasn’t receptive. Perhaps he was too far along in his allopathic cancer treatment (years) and too wedded to his docs’ protocols and their experimentals to try a “last ditch” effort with IVM & FenBen. He died 3 months later. I offered it to another with a “turbo” cancer. Her father (deceased) was an MD so she was stuck in allopathic land. Fortunately she survived, for now, with the removal of the cancerous organ. We have another friend (supposedly) with cancer who still makes noise about wanting more shots because his MD said so. He’s the stubborn type that is not open to suggestions so I just have to hope the train wreck doesn’t happen.
The same thing happens to me. One example is my niece's boyfriend, who has NF1 (Neurofibromatosis 1) , which caused him to have a leg amputated at age 14. Last December, he had a (second) glioma removed from his brain, and was told to expect it to grow back again, faster than it did before. Despite that, when my niece showed him PubMed studies I sent her about IVM and FenBen working well on gliomas (studies posted on this Substack), he is hesitating about trying them, saying that he "will look into it". I guess he prefers having yet another brain surgery instead? I don't get it.
This information is invaluable. I bought a box each of Petmectin & Petdazole just to keep in case I know anyone who needs it. I might keep buying more when I can afford it and keep a little stash for the family.
I'm in Australia and it took about a month to arrive.
I hope you never have to offer this to someone with cancer, but if you do, don’t be surprised if the person doesn’t even engage in a discussion about it. I gave this info on these parasitical drugs to our friend who pretty much wasn’t receptive. Perhaps he was too far along in his allopathic cancer treatment (years) and too wedded to his docs’ protocols and their experimentals to try a “last ditch” effort with IVM & FenBen. He died 3 months later. I offered it to another with a “turbo” cancer. Her father (deceased) was an MD so she was stuck in allopathic land. Fortunately she survived, for now, with the removal of the cancerous organ. We have another friend (supposedly) with cancer who still makes noise about wanting more shots because his MD said so. He’s the stubborn type that is not open to suggestions so I just have to hope the train wreck doesn’t happen.
The same thing happens to me. One example is my niece's boyfriend, who has NF1 (Neurofibromatosis 1) , which caused him to have a leg amputated at age 14. Last December, he had a (second) glioma removed from his brain, and was told to expect it to grow back again, faster than it did before. Despite that, when my niece showed him PubMed studies I sent her about IVM and FenBen working well on gliomas (studies posted on this Substack), he is hesitating about trying them, saying that he "will look into it". I guess he prefers having yet another brain surgery instead? I don't get it.