Guest guest Posted April 11, 2000 Report Share Posted April 11, 2000 From: curtainno1@... Subject: unsubscribe me, please. Please unsubscribe me from your site. Thanks. Hey, Curtain...I don't think you will get unsubscribed with this message--you need to go to onelist to unsubscribe. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 14, 2000 Report Share Posted April 14, 2000 Hi there. I have been reading the many questions coming up @ colonics, colemas, where to get boards, etc. I'd like to recommend a book that I've found extremely useful and have actually given to some members of my family: D r. Jensen's Guide to Better Bowel Care - a complete program for tissue cleansing through bowel management. I bought it @ Amazon.com for about $12.00. It explains the colema process, good solutions to use in your colema and various places to purchase all the equipment you need to get started. Hope this helps. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 12, 2000 Report Share Posted May 12, 2000 HAPPY MOTHER'S DAY TO ALL OF YOU SUPERMOMS OUT THERE!!!!!!!! Love Debbi, mom ot Logan (will be 6 in June) Eli (DS) and Milo (4 in sept) p.s. I would love to see and be on the tape, if we can fix our video cam. My name/address is: Debbi Barer, 22 Farm Road, Weston, CT 06883. Thanks! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 14, 2000 Report Share Posted May 14, 2000 > > Message: 2 > Date: Sat, 13 May 2000 12:12:40 -0700 > From: " Art Brown " <abrown101@...> > Subject: to > > Hello Dr. Moran, > > A question and a comment: > > Have you ever had any experience with this group, or should I say > vigilante posse, called Quackwatch? If so, do you have any comments about > them??? If you've mentioned them in past posts I've missed it. > Every once in > awhile that name comes up. > > I am familiar with Quackwatch and post there regularly. Does it matter? I am a surgeon with a vast experience of cancer and I believe I have shown a great deal of understanding of the problems of the alternative cancer scene, which should matter more. > Now, regarding the interesting and informative, uh, .... dialogs > between yourself and Vince Gammil ..... > > RE: this subject of success figures, also know as the GREAT > GOD DATA in > the sky. Why don't you like data, Art? A testimonial about cancer cure is data. You and your friends gather testimonials and other " data " about alternatives to try and decide which might be worth using. > > I agree it would be helpful to view some sort of figures regarding the > effectiveness of alternative treatments, although I'm sure they would be > immediately and vigorously atttacked by the conventional side as > inadequate, > inconclusive, flawed, concocted or whatever. You need them for yourselves, Art, as well as every cancer sufferer that may go looking for alternatives. > And no doubt Dr. Hulda and Dr. Kelley of nutritional > metabolic theory fame can supply actual meaningful data. >What is > it, between > the two they have about 70 years cancer fighting experience? > > However, I also strongly believe that an overlooked and > important burden > of proof should be upon the all the high paid legal eagles, policy makers, > power brokers, commissioners, lobbyists, regulators etc. that seem to > saturate the conventional medical establishment. > And that is this: BEFORE they be allowed go after alternative > practitioners, guns and badges blazing, they must be able to clearly prove > that alternative treatments are more harmful than conventional. > Nope. The boot will always be on the other foot. The onus of proof is always upon the proponent. This is why you need to sort it all out for yourselves, but you need to be prepared to listen to people telling you what to do. You also need to recognise that many of the criticisms of AM theories and personalities have merit, in the same way as there are half-truths in what AM says about conventional medicine. Moran Sigh, but that would be asking for the moon! > > - Art > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 14, 2000 Report Share Posted May 14, 2000 I am very interested in the pH therapy & calcium & cesium. Barefoot's book, Death by Diet, was some of the first information that I received after my diagnosis. When I received the roll of testing paper, my whole family & I immediately did the test. my husband's & three children, ages 25, 18 & 15 all tested VERY BLUE(7.0-7.4). my test was between 5.5 & 6.0. I used cesium for about 4 weeks, at which time I noticed the signs of a slight numness around the mouth and stopped. I also sought out an herbalist who did a Biological Terrain Assessment, perscribed a strict diet for 90 days, distilled water (which I was already doing) deep breathing, exercises and lots of supplements, etc. We have done a number of AMAS tests, which were some of the first done in this area. My history is: June 9, 1998 - discovered a lump in my breast June 19, 1998 - biopsy July 3, 1998 - lumpectamy. diagnosis: infiltrating duct cell carcinoma of the breast metastatic to seven of 12 axillary nodes. The lesion was 1½ cm in diameter and was Estrogen receptor positive, Progesterone receptor negative, and had both diploid and aneuploid and hyper-diploid cell populations and the S-phase could not be calculated The lesion was a Grade III/III Geraldine >Message: 1 > Date: Sat, 13 May 2000 11:50:38 -0500 > From: Jim Dunstone <jdunstone@...> >Subject: Re: VINCENT GAMMIL > >Hi all. I have just been to a seminar where the speaker was a biochemist >by the name of Barefoot. He was very high on the values of >calcium and cesium. The gist of his presentation was that if you can >change the body from acidic to alkaline then you will be disease free >and he indicated that this can be done in five weeks by taking cesium. > >Has anybody come across this gentleman befor or does anybody have any >comments regarding sthe validity of this process. > >Regards, > >Jim > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 25, 2000 Report Share Posted June 25, 2000 I have noticed when I get excited or in a hurry which I would say is stressful to me..LOL!! I get the tremors more and the best way I have found to combat them is to take a deep breath and try to relax. I just sit for a few minutes and take those deep breaths and it seems to work. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 3, 2000 Report Share Posted August 3, 2000 In a message dated 08/03/2000 2:15:07 AM Pacific Daylight Time, egroups writes: << I was also thinking of creating a table at the the forums eGroups page of the foods for O's to avoid and ones that are OK *perhaps* with a column to allow any of us to add comments about each item as necessary. Is there a use for this or will no-one use it? >> I'd use it Steve! Thanks for all your efforts ! -Seattle Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 4, 2000 Report Share Posted August 4, 2000 In a message dated 8/3/00 8:57:42 PM Mountain Daylight Time, lescase@... writes: << I was also thinking of creating a table at the the forums eGroups page of the foods for O's to avoid and ones that are OK *perhaps* with a column to allow any of us to add comments about each item as necessary. Is there a use for this or will no-one use it? >> >> I think it is a great idea. I would definitely use it and contribute also. Pam from ID Pamacs Selkirk Rex Home of GRCH Pamacs Winnie The Blue The first CFA Grand Champion Selkirk Rex Check out my home page at http://hometown.aol.com/sharpcats/myhomepage/index,html Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 4, 2000 Report Share Posted August 4, 2000 In a message dated 8/4/00 9:56:57 AM Eastern Daylight Time, Sharpcats@... writes: << << I was also thinking of creating a table at the the forums eGroups page of the foods for O's to avoid and ones that are OK *perhaps* with a column to allow any of us to add comments about each item as necessary. Is there a use >> I'll go there, and check it out. I think it's a good idea. Thanks Ann in Fla Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 13, 2001 Report Share Posted October 13, 2001 > .Hmm. I wonder if I had told him > that they were GEORGE CLOONEY'S babies if he would have jumped at the > opportunity? > > Amber ;^) Maybe you should try that with a female doc??? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 28, 2002 Report Share Posted February 28, 2002 Sorry Vicky I haven't seen any post from you of late.... & I was offline & sick for -(real sick) for about the last 6 months.....had encephalopathy bouts(which are just horrible as you're awake but have no memory whatsoever of what's going on around you- even what you've been thinking & saying...finally it gets so bad every one thinks you're speaking some sort of alien tongue & I don't mean like from another but from outer space-- that's when I ended up in the hospital-- they kept asking me ?'s and every time I'd give a different answer My husband & friends told me about later when I was able to think & remember-- but to this day I couldn't/can't remember anything about those times And I really feel lostabout....I just thank the Lord I didn't try & go out driving & I didn't fall down my stairway in the house & outside of house...but I did do some really screwy things form what I've heard! arlene VicLea227@... wrote: > I know laughter is great and all that. I've been keeping up with all going > on and it just seems that there is not much discussion regarding hep c > lately. It also seems to me that there is a core group of members that go > back and forth which seems to leave others out. Maybe I'm being a little > self centered but I know that there are times that I post and no one responds > to me (maybe because I'm not good and quick with words). I'm just sharing my > honest feelings. I haven't posted lately cause I haven't been feeling a part > of. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 28, 2002 Report Share Posted February 28, 2002 Hi Dennis Good to hear from you again......sap for Maple Syrup??? Man I could sure use some of that...... Last year I ran out of the Maple syrup that one of the travel guys from New England brought to Oregon--he gave Ken a couple of jugs of it....but he went back home sometime back arlene Dennis wrote: > Hi Vicky > > As you know, we all have our own personalities and life styles here. I > think that helps keep this group interesting and personal. We kind of know > and respect each other for these differences. I am on another group but > don't read it much or contribute just because it is very clinical and > impersonal. I don't post much because I am not knowledgeable enough to > advise anyone. I also work a full time job and have chores to do before and > after work. After the evening chores and meal I am done in and don't have > the energy to writer -or even read sometimes. Please enter in here where > your interest lies and I'm sure you will get support. > I appreciate hearing from all of you. > TGIF and no major storms this weekend. I was out in the field Yesterday and > saw a pair of Bluebirds! > The sap buckets are out and Spring is on its way. > > Hang in there everyone > Dennis from NH > > Re: [ ] Digest Number 336 > > > I know laughter is great and all that. I've been keeping up with all > going > > on and it just seems that there is not much discussion regarding hep c > > lately. It also seems to me that there is a core group of members that go > > back and forth which seems to leave others out. Maybe I'm being a little > > self centered but I know that there are times that I post and no one > responds > > to me (maybe because I'm not good and quick with words). I'm just sharing > my > > honest feelings. I haven't posted lately cause I haven't been feeling a > part > > of. > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 28, 2002 Report Share Posted February 28, 2002 Machelle DITTO from me also You've(everyone) has to remember WE are living thru this disease & most all Drs have no idea what it is to go thru what we have to deal with day-to-day-----hour-to-hour They get their info from textbooks & we seem to learn from each other----a lot of people don't understand or comprehend the the medical lingo as WE didn't go to school to get our info!!! Personally I'd rather have learned it from a textbook than from that transfusion I had years ago arlene Machelle wrote: > I for one am happy with the way the list is. I look forward every morning to > checking my mail from this list. I have never met such a bunch of strong > people. These people have found reasons to laugh and have fun in spite of > having this disease. When I am lost in this list, I don't feel like I'm > sick. I feel like I am with family and friends and not a bunch of doctors. > Ya know even when someone posts the occasional scientific findings or news > articles, I usually skip them. I know I should be reading them to keep up > with what's going on, why I'm going through certain things..etc....The > reason? I'd rather not worry with it, but would rather talk to my friends > on here for the advice...I'm also the kind of person who has a hard time > comprehending what I'm reading when all the words are 10 or more letters > long....lol > Jump in on the conversations, you'll be surprised at what you may learn > just by asking what's on your mind. I'm sure if you have a question, some > one will answer it for you. This list is a support group....we support one > another through EVERYTHING...good or bad.. > > Support has many definitions: > As a verb: > 1. to carry the weight of, hold up ( we all carry the weight of other's > problems.) > > 2. encourage; help (we encourage each other with everything, not just Hep) > > 3. to advocate; uphold (we advocate for our cause) > > 4. to maintain with money or subsistence ( we maintain our livelihood) > > 5. to help prove ; vindicate, etc (we help prove that having this disease > does not make you an outcast) > > 6. to bear, endure (we endure all the good and bad things that have > happened to us with the help from other list members) > > 7. to keep up; maintain ( we maintain our sanity with through this group) > > As a noun: > > 1. a supporting or being supported (everyone here helps support others) > > 2. a person or thing that supports (laughter helps with that support) > > 3. a means of support (this group has been my means of support since > diagnoses) > > Via Webster's Dictionary.... > > I hope I haven't upset you with what I've wrote, that was not my intention. > > Machelle > > Treasure the love you receive about all. It will survive long after your > gold and good health have vanished. > -Og Mandino > Re: [ ] Digest Number 336 > > I know laughter is great and all that. I've been keeping up with all going > on and it just seems that there is not much discussion regarding hep c > lately. It also seems to me that there is a core group of members that go > back and forth which seems to leave others out. Maybe I'm being a little > self centered but I know that there are times that I post and no one > responds > to me (maybe because I'm not good and quick with words). I'm just sharing > my > honest feelings. I haven't posted lately cause I haven't been feeling a > part > of. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 28, 2002 Report Share Posted February 28, 2002 I know laughter is great and all that. I've been keeping up with all going on and it just seems that there is not much discussion regarding hep c lately. It also seems to me that there is a core group of members that go back and forth which seems to leave others out. Maybe I'm being a little self centered but I know that there are times that I post and no one responds to me (maybe because I'm not good and quick with words). I'm just sharing my honest feelings. I haven't posted lately cause I haven't been feeling a part of. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 1, 2002 Report Share Posted March 1, 2002 Vicky, I don't ever remember you posting that I didn't answer you...... The reason this group was started, was because we wanted to feel free to say whatever we wanted to without restrictions..... I have seen people joining in the last few months that actually were scared that they had no chance and with all the laughter and cutting up it has made them come out of their shell and actually feel they are alive and going to live thru this.... I was there at one time, and I wish I had a group like this to come to.... We support each other no matter what, and if you join in it will make you feel apart of the laughter ad tears... We are all in this fight together and I personally have never seen anyone intentionally ignored...... I am sorry you feel this way..... -dz- I hope you are wrong about how you are feeling.... I am still in a great deal of pain and I have been checking in to see what is happening..... I will be saying a prayer for each and every one of you.... Angel Hugs, Diane May Rainbow Dreams Color Your World With Love, Hope, Peace & Unity Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 1, 2002 Report Share Posted March 1, 2002 I'm sorry you have been feeling left out, I personell try to respond to everyone who post on here, maybe not each time. But I try to get to know everyone in the group. This group has given me the support that I needed to face this dragon And I have opened my feeling in here more then I ever have before. Terry --- VicLea227@... wrote: > I know laughter is great and all that. I've been > keeping up with all going > on and it just seems that there is not much > discussion regarding hep c > lately. It also seems to me that there is a core > group of members that go > back and forth which seems to leave others out. > Maybe I'm being a little > self centered but I know that there are times that I > post and no one responds > to me (maybe because I'm not good and quick with > words). I'm just sharing my > honest feelings. I haven't posted lately cause I > haven't been feeling a part > of. > > __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 1, 2002 Report Share Posted March 1, 2002 Hi Vicky As you know, we all have our own personalities and life styles here. I think that helps keep this group interesting and personal. We kind of know and respect each other for these differences. I am on another group but don't read it much or contribute just because it is very clinical and impersonal. I don't post much because I am not knowledgeable enough to advise anyone. I also work a full time job and have chores to do before and after work. After the evening chores and meal I am done in and don't have the energy to writer -or even read sometimes. Please enter in here where your interest lies and I'm sure you will get support. I appreciate hearing from all of you. TGIF and no major storms this weekend. I was out in the field Yesterday and saw a pair of Bluebirds! The sap buckets are out and Spring is on its way. Hang in there everyone Dennis from NH Re: [ ] Digest Number 336 > I know laughter is great and all that. I've been keeping up with all going > on and it just seems that there is not much discussion regarding hep c > lately. It also seems to me that there is a core group of members that go > back and forth which seems to leave others out. Maybe I'm being a little > self centered but I know that there are times that I post and no one responds > to me (maybe because I'm not good and quick with words). I'm just sharing my > honest feelings. I haven't posted lately cause I haven't been feeling a part > of. > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 1, 2002 Report Share Posted March 1, 2002 Being a loosely knit group, we have to police ourselves. I'm glad you are speaking out, we don't want to leave anybody out. For quite some time that core group of individuals was the only thing keeping this board going. Now we have gained quite a few new members and we should be cognizant of that. We like to have fun, but I don't want it to be at anybody else's expense. I will take your thoughts to heart and hope that we can provide a forum that is helpful to ALL it's members. -dz- --- VicLea227@... wrote: > I know laughter is great and all that. I've been > keeping up with all going > on and it just seems that there is not much > discussion regarding hep c > lately. It also seems to me that there is a core > group of members that go > back and forth which seems to leave others out. > Maybe I'm being a little > self centered but I know that there are times that I > post and no one responds > to me (maybe because I'm not good and quick with > words). I'm just sharing my > honest feelings. I haven't posted lately cause I > haven't been feeling a part > of. > > __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 1, 2002 Report Share Posted March 1, 2002 I for one am happy with the way the list is. I look forward every morning to checking my mail from this list. I have never met such a bunch of strong people. These people have found reasons to laugh and have fun in spite of having this disease. When I am lost in this list, I don't feel like I'm sick. I feel like I am with family and friends and not a bunch of doctors. Ya know even when someone posts the occasional scientific findings or news articles, I usually skip them. I know I should be reading them to keep up with what's going on, why I'm going through certain things..etc....The reason? I'd rather not worry with it, but would rather talk to my friends on here for the advice...I'm also the kind of person who has a hard time comprehending what I'm reading when all the words are 10 or more letters long....lol Jump in on the conversations, you'll be surprised at what you may learn just by asking what's on your mind. I'm sure if you have a question, some one will answer it for you. This list is a support group....we support one another through EVERYTHING...good or bad.. Support has many definitions: As a verb: 1. to carry the weight of, hold up ( we all carry the weight of other's problems.) 2. encourage; help (we encourage each other with everything, not just Hep) 3. to advocate; uphold (we advocate for our cause) 4. to maintain with money or subsistence ( we maintain our livelihood) 5. to help prove ; vindicate, etc (we help prove that having this disease does not make you an outcast) 6. to bear, endure (we endure all the good and bad things that have happened to us with the help from other list members) 7. to keep up; maintain ( we maintain our sanity with through this group) As a noun: 1. a supporting or being supported (everyone here helps support others) 2. a person or thing that supports (laughter helps with that support) 3. a means of support (this group has been my means of support since diagnoses) Via Webster's Dictionary.... I hope I haven't upset you with what I've wrote, that was not my intention. Machelle Treasure the love you receive about all. It will survive long after your gold and good health have vanished. -Og Mandino Re: [ ] Digest Number 336 I know laughter is great and all that. I've been keeping up with all going on and it just seems that there is not much discussion regarding hep c lately. It also seems to me that there is a core group of members that go back and forth which seems to leave others out. Maybe I'm being a little self centered but I know that there are times that I post and no one responds to me (maybe because I'm not good and quick with words). I'm just sharing my honest feelings. I haven't posted lately cause I haven't been feeling a part of. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 3, 2002 Report Share Posted March 3, 2002 Vicky I'm sorry if you feel I have left you out..I sure didn't mean to at all..You have been here a slong as the rest of us have and you are a big part of the group..I wish we could hear from ou more like Deb(the wicked one)..See I didn't forget about her either even though I didn't mention her lately.. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 1, 2003 Report Share Posted January 1, 2003 In a message dated 01/01/2003 2:18:04 AM Central Standard Time, autism writes: << My son was on the cover of TIME magazine in May.... and it was a surprise to see him in the this weeks addition of TIME - >> Dear Pam, I saw your son's photo and recognized it immediately as one of " our " children before reading the accompanying description. It was just something about his body english and the beauty of his little face that was so reminiscent of my grandson, Elliot. He is extraordinarily beautiful!! Barbara B Quote Link to comment Share on other sites More sharing options...
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