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Originally Posted by Arrowwind09
I will be interested in hearing about the antiangiogensis therapy. Are you going to try bindweed? What really blew me away about the article is that it helped in very advanced cancer. The Townsend Letter is about equilivant to the Journal of American Medicine in the Alternative health realm.
Has your husband been doing mms?
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Arrow, I feel so bad that I have not been back here to post as I know how important updates are and how hungry people are to read of positive results here. I know I certainly do hunger for others' testimonies.
He had the chemoembolization now a month ago and they did not use Avastin but used doxyrubacin. Just today, a whole week after his last MRI, they called to give us an update (after not returning our calls for a whole week) but didn't really have anything to tell us other than that the tumors are not bigger and they now say they won't know anything til he has lab work.
He was doing a whole lot better before he had the CE. They managed to somehow butcher his leg with the incision for the catheter and he was so drugged up with demerol that he seemed a whole 20 years older after the procedure and still has pain from the incision site, taking hydrocodone for pain in his leg. He isn't taking a lot of them but I wish he didn't have to take any of them. I'm sure he has pain but I can't understand why he should have so much pain this far out and from such a small incision. There was far too much bruising and I feel like they somehow messed up his leg. I don't understand it.
Anyway...I have continued to constantly read and I have learned a lot of things. I don't want anyone to be discouraged about the MMS drops which we did try or any of the other therapies that have worked for some. I think that it is really an individual thing and that one has to find the right thing for their particular condition. I have not seen much on this site about oleander or about pau d arco but I have read extensively about them on many other sites.
The thing is that with the CE, the blood vessels that feed the tumor are blocked with the chemo and so nothing can get to them, nothing at all, for at least the duration of the chemo beads in the vessel. I understand that they last for about a month. So, even oleander or MMS drops or B17 or anything is getting to the tumor. He has been taking (1 week) oleander in the capsules but only in very small doses so as to gradually increase over time. We have ordered some pau d arco tea and I hope it is the real thing (inner bark). I ordered from a vendor called Taheebo Tea Club. Does anyone know of them?
I will let you know how things are going after a week or so of that. He most certainly will NOT be going back for a second round of the CE. Forget it. Thank you very much but no thank you very much.
I do so hope we can regain what has been lost through 'white man's' medicine thus far...but I learned a long time ago that one thing you cannot ever get back is TIME that is lost.
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