9) Mrs N tells of November 2001 to May 24, 2002 how she has gone and now.
dated May 24, 2002: From mrs. N. I received today the sequel to her story above and this is her current situation.
So ... we ... alive! And the quality is high. It is sometimes exciting and sometimes very difficult, but God is what life is beautiful . The iron discipline that you need the supplements to "eat." Them in time order, to your orthomolecular doctor to go, your "regular" oncologist visit, the tension on your lab results, you suddenly needed surgery interim 's. The voltage on your scan results, etc. etc. I then do my meditation Simonton, I pray, my husband gives me my falie me with that hospital conditions / results not trying to be a waste of time. And it works ....!
Surgery in October 2001 (RFA, see RFA-page cancers for all information) in Italy. Dr. Solbiati (Editors note: for those who want to address, send us an email ) had asked after three months I'd like to see a scan. So was my great cooperative oncologist prescribed a scan in the VU. The results (dated December 2001) was that a new metastasis was sitting in the abdomen near a fallopian tube, a small cyst which had to formed (fluid filled) to about 15 cm! I was in Mexico again on holiday: this is the Houtsmuller Country ...: avocado (quacemole), Pineapple, Papaya, which are now in the Netherlands, also available in small size, it is a very important food (fruit) in the fight against cancer, peppers, onions broccoli, alfalfa sprouts and many other programs, watermelon (ordinary other melons are sweet). So when I came back from Mexico was that bad news is to swallow.
The following happened: the oncologist said, "we will fight it with drugs." When I have an oncologist with whom I have often "An other opinion" discussed asked what he thought of it. He immediately said to wegopereren made by a good colleague (not in my hospital (Anthony van Leeuwenhoek)) but by Dr. X in the VU ... The orthomolecular doctor had before. This was so contrary to my attending oncologist at the VU, so my husband and my decision ... Then I have my oncologist at the VU asked if he wanted to make an appointment with that doctor. Dr. X wanted me to immediately operate but "no time and space." Two days later I called and this Dr. X said that the three or four weeks he needs had for me to find a place to operate it would not wait and that I would like to Dijkzicht Rotterdam because there was no waiting list is / was. (that was come to my attention). Result of this call: Five days later I was operated on at the VU by Dr. X. Before then he told me that it is a lot risk was because there was substance of the cyst during surgery leak that he would be well flushed yet, and still more terrible scenarios he painted me the day before my surgery I bought the book by Karin Spaink the chosen death .... While I'm actually a huge optimist, but I just could no longer sit down after that black and heavy story. After surgery, my "operator" at my bedside telling that the area was completely clean, well-managed operation, totally adhered intestines (it is very important) etc etc etc .... Whatever he was told that he was an inch again on the liver metastasis was seen sitting and that he had removed. He also said that on a scan is not even an inch metastasis see ... ..
After six days I was back from the hospital and he was proud of me as soon recovered. But nobody said the medical team would have something to do with the orthomolecular guidance in this patient. For my fitness and blood levels are very good. I had my fish boxes with supplements on the table beside my bed and got the Houtsmuller Diet in VU.Visdozen are ideal: for every day and every time. My tumor markers were dropped to 7, but two weeks later increased to nine. In other words, there was something active again. Then I oncologist who in Anth. Van Leeuwenhoek Hospital asked what to do. It was this time no phone call, but an oral advice. And this time he was very rude to my husband and me. Now know my husband a lot about cancer and the matter combat (he has access to key information) so he wanted with this doctor. NO WAY! He was very annoyed that we do not unquestioningly assumed what he said, there are namely several types of chemotherapy and combinations. Xeloda (see below) (editors note: if a copy will of a Phase III trial of Xeloda - also called capecitabine mentioned send me an email or order it directly from physician / oncologist at Roche Netherlands. See cancers, colon cancers for describing what capecitabine or Xeloda is) he had never heard at all. His advice was very heavy chemo, he said, terrible side effects. Then my husband said "And how long has my wife still living? "Then he said:" Another four months. " This conversation took place exactly four months ago place and I have a very good condition. My tumor markers are present below the 5 (...) and the scan was made last week says that my lungs, pelvis and bones are clean and that the "cooked" so burned away in the liver metastases became smaller again. (This is truly a wonder-not only for Dr. Solbiati ... .-). It is really in the report of the scan but the oncologist in the AVL. I must be gone .... You do not believe it ?????????!!!!!!!!
My husband and I were so upset about the treatment of this doctor in AVL I immediately the next day there organized scan and other tests have been canceled. It was the administration of that department (poly oncology) urged me if I have a complaint about this doctor wanted to submit. The names of two people were given to me ... ... I did not. I do have a record of the "conversation" and that made the doctor sent. ... In it I wrote him that I already was aware of the fact that he has close links with the Association against Quackery. (Editors note: This doctor does have close ties with the Association against Quackery and is bandied about in the media for its positive opinion on regular chemotherapy and are very strong negative opinion of 'alternative / complementary "to give. A bad thing because it never mentions that he made close ties with the Association against Quackery. This is often in the media the impression that a regular oncologist with a certain status objective information about specific treatments. is pure deception by a respected 'oncologist). The fanaticism with which he discussed his idea about my chemo, authoritarian mode of treatment, I gun it is not patient. You'll only be his patient ..! He has written back and went into nowhere: only defense. Another letter from me to see him again. Kees Braam has copies of this correspondence. Orthomolecular therapy, supplements: "all rubbish" according to this doctor.
By now I was back at my pretty knowledgeable, patient Cooperative oncologist at the VU (I still support multiple opinions, because doctors are also not all agree with each other about the strategy as we know, and we must also be informed as is evident from the various opinions in my case alone) . Incidentally, my oncologist was interested in the VU, friendly. What a great man! He told me that the tumor markers of me being cancer activity from 7 to 9 again. It's nothing that I know but he still wanted me to do chemo went well and Xeloda, which is a way you can swallow! That was my husband asked him four months earlier but then it was not known in the VU. In America this for three years but apparently we have used in the Netherlands the wheel. Now I use it for almost two months with great effect mentioned above. This product is of course not heaven, because your hands are red skin (may very) thin so quickly gaps (there will Xeloda an ointment advice) and the skin of the feet is very thin so very good soft shoes and a good foot care law with cut nails. And you can get diarrhea and then the amount reduced. But ... .... it is compared with chemo-infusion in the hospital a world of difference because you're basically once every three weeks for checks to your oncologist. And the effect is better. A very important informative story about the amount of Xeloda that you could / should swallow. There, my husband and orthomolecular doctor talked with each other.
Now, I'm back further in time and I I intend to continue what I've been doing so far, especially with the Simonton Meditation, something interpreted by myself. Incidentally, I have about three conversations with a therapist Simonton had been increasingly uncomfortable. Moreover, such a conversation rather expensive. My first idea is the first book of Simonton to read that is very instructive, and perhaps sufficient. (Editors note: Simonton comes in the summer of 2002, so very soon to see the Netherlands page other alternatives under Simonton therapy) Memories from a therapist has actually been a good first interview (click) else better to find another, there are plenty. The support that I have the information from the site of Kees Braam make us as (ex-) cancer patients are empowering. Especially to the doctors because of their overloaded, there is little or no communication between them and that is a definite problem. The doctors must sometimes their information from their patients! Let us keep you informed if at all possible; about our diet, our doctors, our experiences in hospitals, etc. etc. etc. Also a member from view, the journal of the Association Moerman . can be good. (or join OPS see page OPS) It costs almost nothing and there are such encouraging stories and all other important matters. (Editors note: We also have a free email group for those with peers on issues relating to cancer will email / exchange. send me an email and I write for free, now about 40 members)
A. dated May 24, 2002, N.
