Hello Dave,
Please let me start by explaining that Rachel and I are both retired and our "expertise" in alternative and complementary treatment is limited to information gathered over the past 6 months, is not based on expert knowledge, and any statements should not be taken as medical advice.
My personal gain from Rachel's illness is the discovery of how much more than surgery and chemotherapy is available, and useful, in the management of cancer. I very much regret not having come to this realisation at a time when it might have been useful to my patients, and really hope that the "integrative medicine" takes off and allows the coexistence and amalgamation of all useful therapies. We may need to ditch the term "alternative medicine" first, because it is a divisive one.
Prior to looking at the RECNAC website my main reference to Vitamin C was Dr Abraham Hoffer and you will find a lot of hits in Google under "Abraham Hoffer and Vitamin C and Cancer". It certainly seems to have some value, but as you have discovered, we need to find a form which is not as readily excreted by the body and is still safe to use from the point of view of overdosage. This problem seems to place some limits on the value of this as a mainstay treatment, but if it is making an obvious difference to your wellbeing why abandon it?
Theoretically I was impressed by the alkalinisation idea as in Caesium and Ionised Water. How bad was your problem with Caesium? Oxygen therapy was another treatment which appeals for having an effect without apparent side effects. And as you know there are many more, we are giving Rife a go as well. There is no need to limit yourself to any one method.
Tetrathiomolybdate is someting which has an effect on angiogenesis and may counteract the pulmonary fibrosis associated with Iressa - I have no idea if it has been trialled in this way as yet.
Please do not take my statements as medical advice. They are comments made on topics which are quite new to me and I will continue trying to lessen my ignorance for a long time yet.
Best wishes,
Karel.
Thought I should add my two cents worth as the patient! I would certainly endorse what Karel says about our lack of expertise on so-called alternative therapy. Despite medical training, I found myself in exactly the same position as all other Stage 4s and doing the same running around looking for answers. One thing which becomes very obvious, to misquote George Orwell, is that some Stage4s are more equal than others, and this of course translates to the varied reactions we have to treatments; for example, I'm about to start my fifth cycle of Cisplat and Gemcitabine, and have had fairly mild side effects, also Caesium didn't bother me except for mild nausea. I take vitamins, minerals and enzymes on the advice of nutritionists and others who have spent much longer than myself researching the topics, and I keep my oncologist informed on what I'm doing; I've also changed my diet to get rid of sugar, as little salt as possible{preferably potassium chloride }, as little fat as possible, and protein from vegetable or white meat and fish sources. So far the situation remains stable, but we continue to look for anything useful and apparently sensible. Many people in our situation do manage to beat the odds, and a forum like this is excellent for exchanging information and hope, providing we all remember that even if we become experts in our personal situation, we still must rely on the objective advice from the specialists in their own fields.
All the very best, Rachel.