Guest guest Posted June 17, 2004 Report Share Posted June 17, 2004 Essiac(sp?) Tea Geoff Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 22, 2004 Report Share Posted June 22, 2004 Don't know if this is the same person, but a friend of mine forwarded this answer to me: Her name is Dr. Lorraine Day @ drday.com. Dr. Day advocates a 10-step program for health, which includes juicing, vegetarian diet, drinking lots of water, exercise, etc rheumatic Cancer Treatment Do any of you remember back about 6 yrs ago when Ethel posted information about a liquid you could take that reduces/eliminates cancerous tumors in the body? There is also a female doctor that has a web site advocating this. I believe she treated her own breast tumor. Maybe one of you have this saved on your computer. Appreciate your help! Lea To unsubscribe, email: rheumatic-unsubscribeegroups Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 22, 2004 Report Share Posted June 22, 2004 Are you talking about Essiac tea? I believe that's named after a female Dr who lived in Canada by the name Caisse (Essiac spelled backwards.) Kimmie Message ----- From: " Ellen McCool " <ellenmccool@...> <rheumatic >; " leatanner " <leatanner@...> Sent: Tuesday, June 22, 2004 12:43 AM Subject: Re: rheumatic Cancer Treatment > Don't know if this is the same person, but a friend of mine forwarded this answer to me: > > Her name is Dr. Lorraine Day @ drday.com. Dr. Day advocates a 10-step program for health, which includes juicing, vegetarian diet, drinking lots of water, exercise, etc > rheumatic Cancer Treatment > > > Do any of you remember back about 6 yrs ago when Ethel posted > information about a liquid you could take that reduces/eliminates > cancerous tumors in the body? There is also a female doctor that > has a web site advocating this. I believe she treated her own > breast tumor. Maybe one of you have this saved on your computer. > Appreciate your help! > Lea > > > > > To unsubscribe, email: rheumatic-unsubscribeegroups > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 28, 2004 Report Share Posted July 28, 2004 Well, from what I've read so far... you're still talking about a semi-synthetic compound -- Those two words right there do it for me.... it ain't natural....lol... I think I'll stick to the All-natural and leave the semi-synthetics alone. I'll get thru the rest of it later today... I know it does sound like something I've heard of before but can't place it at the moment. Suzi <drcrandall@...> wrote: A patient said that a friend is going for this treatment. It looks really pricey for an alternative, if that's what it is. The method sounds familiar but I can't place the therapy that it resembles.What are your opinions?www.heatkillscancer.com Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 30, 2004 Report Share Posted July 30, 2004 Thanks Suzi for the input. It is definitely not natural and looks like a quick fix...for the vendor's pocketbook. But then again DMSO is not natural is it? I guess it's the price that makes it really questionable. Most natural cancer treatments don't go over $3000 that I know about. I'll let you know how the woman that has gone for the treatment makes out. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 30, 2004 Report Share Posted July 30, 2004 wrote: > Hi, everybody, > > Been on holiday, trying to catch up. This is one busy group...lots > of new faces! > > A patient said that a friend is going for this treatment. It looks > really pricey for an alternative, if that's what it is. The method > sounds familiar but I can't place the therapy that it resembles. > > What are your opinions? > > www.heatkillscancer.com > > > -=-=-=-=-=-=-=-=-=-=-=-=-=-= I have no doubt as to the efficacy of this drug. However, the synthetic chemotherapeutic agent would scare me off. The Greater Celandine, however, would be quite useful all by itself. Anyway, sounds like chemical microwaving of the cancer cells. -- Peace, love and light, Don Quai " Spirit sleeps in the mineral, breathes in the vegetable, dreams in the animal and wakes in man. " Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 26, 2006 Report Share Posted March 26, 2006 Hi Rogene, I don't get to check my email very often between work, the ranch and living so I am not very prompt to get answers out. : ) My cancer dr. wanted me to take chemo and then tamoxifen but that would have meant another surgery to put the port in, then 3-6 months of having and recovering from chemo and later another surgery to take the port back out. I didn't want to waste any part of my life " fighting " cancer, I just wanted to enjoy living for the time being and so I chose only to take tamoxifen. I didn't notice if that is the same drug you are on but so far I have be taking it for about 45 days and no real side effects yet. Time will tell. Polly Message: 18 Date: Fri, 24 Mar 2006 07:50:58 -0800 (PST) From: Rogene S <saxony01@...> Subject: Re: Re: Fw: implants.....please help: Hi Lea, Treatments are over . . . ten treatments over five days. No burns, no fatigue. Just a little sore where the balloon was. I'm trying the estrogen blocker the doctors recommend. I have some serious questions about it! . . . According to studies, it reduces the risk of cancer reoccuring from about 20% to less than 2%... Probably better than that of the general population. However, the major side effect is joint/muscle pain/stiffness. .. . And I'm feeling some of that. I woke up with a headache yesterday and today, I hurt from the top of my shoulders to the base of my skull! Still, I'm going to give this stuff a chance. One of my friends took part in the initial study. Her only effect was some hot flashes. They told her she could quit taking it after five years. All in all, I'm doing really good! Don't worry about me! Love, Rogene Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 26, 2006 Report Share Posted March 26, 2006 Hi Polly, Tamoxifen was ruled out for me . . . history of blood clots. . . However, the one they prescribed isn't working very good . . . Today, I'm having pain in what appears to be my kidneys. I'm not taking it again until I talk to the doctor - and maybe not then! I've had more discomfort from the medication than I did with the lumpectomy or radiation combined. They said there were other options. I like the idea that it can reduce reocurrance from 20% to less than 2% . . . But I'd rather take my chances if it means hurting like this! Hugs, Rogene --- northdak76 <northdak76@...> wrote: > Hi Rogene, > > I don't get to check my email very often between > work, the ranch and > living so I am not very prompt to get answers out. : > ) > > My cancer dr. wanted me to take chemo and then > tamoxifen but that > would have meant another surgery to put the port in, > then 3-6 months > of having and recovering from chemo and later > another surgery to take > the port back out. I didn't want to waste any part > of my > life " fighting " cancer, I just wanted to enjoy > living for the time > being and so I chose only to take tamoxifen. I > didn't notice if that > is the same drug you are on but so far I have be > taking it for about > 45 days and no real side effects yet. Time will > tell. > > Polly > > Message: 18 > Date: Fri, 24 Mar 2006 07:50:58 -0800 (PST) > From: Rogene S <saxony01@...> > Subject: Re: Re: Fw: implants.....please help: > > Hi Lea, > > Treatments are over . . . ten treatments over five > days. No burns, no fatigue. Just a little sore where > the balloon was. > > I'm trying the estrogen blocker the doctors > recommend. > I have some serious questions about it! . . . > According to studies, it reduces the risk of cancer > reoccuring from about 20% to less than 2%... > Probably > better than that of the general population. However, > the major side effect is joint/muscle > pain/stiffness. > . . And I'm feeling some of that. I woke up with a > headache yesterday and today, I hurt from the top of > my shoulders to the base of my skull! Still, I'm > going > to give this stuff a chance. One of my friends took > part in the initial study. Her only effect was some > hot flashes. They told her she could quit taking it > after five years. > > All in all, I'm doing really good! Don't worry about > me! > > Love, > > Rogene > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 27, 2006 Report Share Posted March 27, 2006 I talked to the doctor's nurse again today . . . She wants me to continue with the medication and see if the side effects pass with time. . . I'm to take Motrin, rather than the Tyenol I was taking. I'm not happy about it. But, I'm working with a top oncologist, so I'm going to keep trying. Today was the pits though! Love, Rogene Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 27, 2006 Report Share Posted March 27, 2006 Hi Rogene, I hope you start feeling better very soon! Kenda > I talked to the doctor's nurse again today . . . She > wants me to continue with the medication and see if > the side effects pass with time. . . I'm to take > Motrin, rather than the Tyenol I was taking. I'm not > happy about it. But, I'm working with a top > oncologist, so I'm going to keep trying. > > Today was the pits though! > > Love, > > Rogene > > > > > Opinions expressed are NOT meant to take the place of advice given by licensed > health care professionals. Consult your physician or licensed health care > professional before commencing any medical treatment. > > " Do not let either the medical authorities or the politicians mislead you. > Find out what the facts are, and make your own decisions about how to live a > happy life and how to work for a better world. " - Linus ing, two-time > Nobel Prize Winner (1954, Chemistry; 1963, Peace) > > See our photos website! Enter " implants " for access at this link: > http://.shutterfly.com/action/ > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 27, 2006 Report Share Posted March 27, 2006 Hi Rogene, I wish you well, and am sorry to hear that the meds are causing you discomfort. Good luck to you. Sis > > I talked to the doctor's nurse again today . . . She > wants me to continue with the medication and see if > the side effects pass with time. . . I'm to take > Motrin, rather than the Tyenol I was taking. I'm not > happy about it. But, I'm working with a top > oncologist, so I'm going to keep trying. > > Today was the pits though! > > Love, > > Rogene > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 16, 2008 Report Share Posted September 16, 2008 > > Dear Friends, > > I am a new member of this group, and I heard about this drug from a > doctor, who practices both alopathic, and alternative medicine. Below > is a brief description of the case for which this drug is considered > as > a part of the treatment protocol. > > My 80 year old father was diagnosed with the squamous cell carcinoma > on > the left chick that was surgically removed 2 years ago. Four months > ago > he discovered some swelling behind the left ear. MRI showed > metastases > in multiple lymphatic nodes of the left salivary (parotid) gland > infiltrated into some surrounded tissues. The did the biopsy in July > that confirmed the stage IV SCC diagnosis. The surgery was done on > 8/6. > The gland and some surrounding tissues along with a part of facial > nerve were removed. No distant metastasis has been found. We were > told > that radiotherapy was absolutely necessary, and my father will start > it > in a week. He is still in a very good physical shape (takes only > avalite, meclizin, and baby aspirin) and walks daily several miles, > but > after the surgery fatigue is very noticeable. He also follows a > healthy > mostly vegetarian diet (simplified Budwig), takes oleander extract, > essiac tea, and some ayurvedic preparations. > > Has someone had some information/experience with this type of cancer? > > We would greatly appreciate any comments or advice, especially if > it's > based on personal experience. > > Best Regards, > Nekto >============ Yes, my grandmother. Go to the link below and look at the 3rd post about my grandma. Click on that topic to open. The link below is to personal stories on my LDN forum. http://ldn.proboards3.com/index.cgi?board=personal Quote Link to comment Share on other sites More sharing options...
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