Guest guest Posted June 12, 2006 Report Share Posted June 12, 2006 Interesting timing. For awhile now I have been thinking of the list as it was. I joined around 1996, I believe. I often wonder about some of the listers. a P. posts once in a while, Ute just recently and the Fairy Lady. Geoff is quiet. Joe G. and Janet in Tulsa apparently are managing. I wonder about C., Liz G., Bev in Ontario, Ray B., Dr. Chiu. No doubt I have missed some folks. We were a community. Don't even hear about Dr. Franco either. Pray the ry ---------- No virus found in this outgoing message. Checked by AVG Free Edition. Version: 7.1.394 / Virus Database: 268.8.3/360 - Release Date: 6/9/2006 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 12, 2006 Report Share Posted June 12, 2006 I one from way back and was very active with posoting. Probaly seven years or so. Unfortunately the AP was not for me and after five years I sustained great joint damage. I only email privately since my experiences are not all positive and some messages need to be handled only with the person. I still read the posts to see how the " old timers " on the AP are doing, and still email several at their personal addresses. I wrote some of the ex-members from an old list that I had and asked it they still were on AP and how they were doing, and never heard a word. rheumatic re: group > > > Interesting timing. For awhile now I have been thinking of the list as it was. I joined around 1996, I believe. > I often wonder about some of the listers. a P. posts once in a while, Ute just recently and the Fairy Lady. Geoff is quiet. Joe G. and Janet in Tulsa apparently are managing. I wonder about C., Liz G., Bev in Ontario, Ray B., Dr. Chiu. No doubt I have missed some folks. We were a community. > Don't even hear about Dr. Franco either. > > > Pray the ry > ---------- > > No virus found in this outgoing message. > Checked by AVG Free Edition. > Version: 7.1.394 / Virus Database: 268.8.3/360 - Release Date: 6/9/2006 > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 12, 2006 Report Share Posted June 12, 2006 Hi ; I joined in 1998,have Scleroderma,doc said I would die within the year.HA! I am doing just fine thank you,about 98% normal.Had to get off the MTX and could not do it until I got the Celiac and vit.D controled then the AP kicked in just fine. Lynne G. wrote: > I one from way back and was very active with posoting. Probaly seven years > or so. Unfortunately the AP was not for me and after five years I > sustained > great joint damage. I only email privately since my experiences are > not all > positive and some messages need to be handled only with the person. I > still > read the posts to see how the " old timers " on the AP are doing, and still > email several at their personal addresses. > > I wrote some of the ex-members from an old list that I had and asked > it they > still were on AP and how they were doing, and never heard a word. > > > > rheumatic re: group > > > > > > > Interesting timing. For awhile now I have been thinking of the list > as it > was. I joined around 1996, I believe. > > I often wonder about some of the listers. a P. posts once in a > while, > Ute just recently and the Fairy Lady. Geoff is quiet. Joe G. and Janet in > Tulsa apparently are managing. I wonder about C., Liz G., Bev in > Ontario, Ray B., Dr. Chiu. No doubt I have missed some folks. We were a > community. > > Don't even hear about Dr. Franco either. > > > > > > Pray the ry > > ---------- > > > > No virus found in this outgoing message. > > Checked by AVG Free Edition. > > Version: 7.1.394 / Virus Database: 268.8.3/360 - Release Date: 6/9/2006 > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 12, 2006 Report Share Posted June 12, 2006 Congrats! I sure wish that my aunt had been able to have the same option of being able to use the AP in the 70's. Oh believe me, I know it works for many. I went to one of the best docs in the country for the AP for several years, but for me it didn't stop the damage. Good to see that you are still participating in the group! rheumatic re: group > > > > > > > Interesting timing. For awhile now I have been thinking of the list > as it > was. I joined around 1996, I believe. > > I often wonder about some of the listers. a P. posts once in a > while, > Ute just recently and the Fairy Lady. Geoff is quiet. Joe G. and Janet in > Tulsa apparently are managing. I wonder about C., Liz G., Bev in > Ontario, Ray B., Dr. Chiu. No doubt I have missed some folks. We were a > community. > > Don't even hear about Dr. Franco either. > > > > > > Pray the ry > > ---------- > > > > No virus found in this outgoing message. > > Checked by AVG Free Edition. > > Version: 7.1.394 / Virus Database: 268.8.3/360 - Release Date: 6/9/2006 > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 13, 2006 Report Share Posted June 13, 2006 Dave, this site is devoted to the antibiotic protocol. I would highly suggest that you peruse the entire site and look at the established protocol there. Then, read the stories of the people there. I am WAY behind on updating my story which is there as I am one of the SD patients whose tests are now negative and I feel great. It has been a long and steady journey. READ the suggested diets and take the seriously. Read and follow suggestions for supplements. and first and foremost, go to amazon.com or one of the bigger bookstores and order two books and read them thoroughly. Both books are by Dr. McPearson Brown and Henry Scammel. The first is THE NEW RHEUMATIC BREAKTHROUGH and the second is SCLERODERMA: THE TREATMENT THAT CAN SAVE YOUR LIFE. I read and carried these books around like bibles as they came me direction and hope. Best of luck to you. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 13, 2006 Report Share Posted June 13, 2006 I STAND CORRECTED!!!! YOU ARE RIGHT! IT IS SCLERODERMA: THE PROVEN THERAPY THAT CAN SAVE YOUR LIFE. It is a small book and I still recommend both but for the SDers, it gives a personal approach to a deadly disease. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 13, 2006 Report Share Posted June 13, 2006 The Fairy Lady (dermatomyositis) made a complete recovery after changing her diet and incorporating detoxing as part of her therapy. Upon remission she studied to be a nutritionist and now has her own shop. Ethel rheumatic re: group > > > Interesting timing. For awhile now I have been thinking of the list as it > was. I joined around 1996, I believe. > I often wonder about some of the listers. a P. posts once in a while, > Ute just recently and the Fairy Lady. Geoff is quiet. Joe G. and Janet > in Tulsa apparently are managing. I wonder about C., Liz G., Bev in > Ontario, Ray B., Dr. Chiu. No doubt I have missed some folks. We were a > community. > Don't even hear about Dr. Franco either. > > > Pray the ry > ---------- > > No virus found in this outgoing message. > Checked by AVG Free Edition. > Version: 7.1.394 / Virus Database: 268.8.3/360 - Release Date: 6/9/2006 > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 13, 2006 Report Share Posted June 13, 2006 Hi Ethel. Can you tell me what is a good detox method. Thanks. Ethel Snooks <emsnooks@...> wrote: The Fairy Lady (dermatomyositis) made a complete recovery after changing her diet and incorporating detoxing as part of her therapy. Upon remission she studied to be a nutritionist and now has her own shop. Ethel rheumatic re: group > > > Interesting timing. For awhile now I have been thinking of the list as it > was. I joined around 1996, I believe. > I often wonder about some of the listers. a P. posts once in a while, > Ute just recently and the Fairy Lady. Geoff is quiet. Joe G. and Janet > in Tulsa apparently are managing. I wonder about C., Liz G., Bev in > Ontario, Ray B., Dr. Chiu. No doubt I have missed some folks. We were a > community. > Don't even hear about Dr. Franco either. > > > Pray the ry > ---------- > > No virus found in this outgoing message. > Checked by AVG Free Edition. > Version: 7.1.394 / Virus Database: 268.8.3/360 - Release Date: 6/9/2006 > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 13, 2006 Report Share Posted June 13, 2006 Treatment Than Can Save Your Life, but they do have one by Henry Scammel titled The Proven Therapy That Can Save Your Life. Is this the book that you have. I would very much like to buy it, but would like the one that you are talking about. Thanks ever so much. Sltfain@... wrote: Dave, this site is devoted to the antibiotic protocol. I would highly suggest that you peruse the entire site and look at the established protocol there. Then, read the stories of the people there. I am WAY behind on updating my story which is there as I am one of the SD patients whose tests are now negative and I feel great. It has been a long and steady journey. READ the suggested diets and take the seriously. Read and follow suggestions for supplements. and first and foremost, go to amazon.com or one of the bigger bookstores and order two books and read them thoroughly. Both books are by Dr. McPearson Brown and Henry Scammel. The first is THE NEW RHEUMATIC BREAKTHROUGH and the second is SCLERODERMA: THE TREATMENT THAT CAN SAVE YOUR LIFE. I read and carried these books around like bibles as they came me direction and hope. Best of luck to you. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 13, 2006 Report Share Posted June 13, 2006 From: " Rizun " <eorizun@...> Sent: Tuesday, June 13, 2006 10:30 AM Hi Ethel. Can you tell me what is a good detox method. That depends on the area you are detoxing because each area requires something different. It is thought best to start with a good bowel cleanse - one that will remove the impacted fecal matter - and repeat it again later. Colonics would be an excellent way to detox the bowel. You can ask at any good health food store and they should be able to tell you who offers this service in your area. I remember an RA patient in Texas telling me how many pounds she lost doing 5 days of colonics. She drank a lot of organic apple juice before and during the therapy. After the series was completed, a good probiotic was implanted to replace any good bacteria lost in the procedure. Other colon therapists offer herbs to clean the bowel. www.blessedherbs.com has a kit for several hundred dollars. Remember, 70% of immune function takes place in the gut. When it's out of balance - watch out! The well known herbalist, Dr. Schulze has a good oral bowel cleanse called Intestinal I and Intestinal II. It's reasonable and effective. I go through cleanses at least every six months and sometimes use this one. www.herbdoc.com. You need to drink a LOT of water with this or any other such cleanse. The doctors I know who prescribe cleanses do a parasite cleanse before doing a liver/gallbladder cleanse. I've used Dr. Hulda 's parasite cleanse (http://www..net/info/p_chart.htm) and also Premier Research Labs' Parastat and Paracidin starting with one capsule three times a day and building up to three capsules three tmes a day. I know these give results so I stick with them. There are a number of good liver/gallbladder cleanses on the net but the one I like best was given to me by a doctor who battled breast cancer metastcized to the bone, followed by what she diagnosed as MCTD. This was one sick doctor when I met her. Her arms and legs were hard and bronze colored. I introduced her to the AP protocol and she was juicing and detoxing. She also did DMSO IVs after learning about them from Dr. s at Oregon State University. I will post this liver cleanse separately. You need to repeat this cleanse until you clean the area out. You will be amazed at what you see and how much of it is there. You also need to consider being tested for heavy metal toxicity. www.gsdl.com. Intravenous chelation is sometimes used and then there is another product giving good results called - PCA-Rx by Maxam Neutraceutics - www.maxamlabs.com It is said to act as a chelator of heavy metals, cardio and vascular plaque, removes toxins and help rid body of mycoplasmas. Dosage is 1 to 8 oral sprays - mist (trans-mucosal) 1 or more times daily Another good product winning good reviews is NDF and NDF Plus from BioRay, Inc. www.bioray2000.com Dr. recommends the following: Blend in blender - 1 clove garlic ½ cup almonds, cashews or other nuts 1 cup packed fresh cilantro leaves 2 tablespoons fresh lemon juice 6 tablespoons olive oil Two teaspoons a day for two to three weeks. Freezes well so make several batches. (Liquid 3 to 1 ratio of oil to juice. Add touch of hot water to scrape blender. Check for neurotoxins often present in chronic disease. www.chronicneurotoxins.com. There is a visual test on this site you can take for a nominal fee. Several years ago a doctor handed me a brochure about a place (I think) called Blueberry Hill. He said one of his patients had gone there and in 7 days (!) had made a remarkable recovery from a debilitating illness. (I've forgotten the diagnosis. Blueberry Hill was a home surrounded by landscaped acreage - a very quiet, serene place. You were not allowed to talk on the phone, see friends or family, or do any work.) The doctor decided to send another patient, and then another, and the same thing occurred. He told me he was so impressed he was going to take a week off and go himself. What was the therapy? Detoxing the body and enhancing the immune system through diet and supplements. My daughter, a nurse, tells me back in the early 70s, one of the first things they did when a patient was put in the hospital was to give them an enema. She said you would be surprised at how many patients recovered from their illness after the enema, but this practice was stopped years ago. Please let me know if something isn't clear or you have questions. Ethel Ethel Ethel Snooks <emsnooks@...> wrote: The Fairy Lady (dermatomyositis) made a complete recovery after changing her diet and incorporating detoxing as part of her therapy. Upon remission she studied to be a nutritionist and now has her own shop. Ethel rheumatic re: group > > > Interesting timing. For awhile now I have been thinking of the list as it > was. I joined around 1996, I believe. > I often wonder about some of the listers. a P. posts once in a while, > Ute just recently and the Fairy Lady. Geoff is quiet. Joe G. and Janet > in Tulsa apparently are managing. I wonder about C., Liz G., Bev in > Ontario, Ray B., Dr. Chiu. No doubt I have missed some folks. We were a > community. > Don't even hear about Dr. Franco either. > > > Pray the ry > ---------- > > No virus found in this outgoing message. > Checked by AVG Free Edition. > Version: 7.1.394 / Virus Database: 268.8.3/360 - Release Date: 6/9/2006 > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 14, 2006 Report Share Posted June 14, 2006 I see some of the people posting on the two other sites I know of. The biggest problem is that when we get our lives back and feeling great again, it is easy to forget about the sites. I am as guilty as others. I post mostly on this site as it comes to my email. Others I only visit occasionally now. I feel a bit guilty but am so busy with doing all the things I never thought I would do again. Just need more hours in the day. Martha Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 14, 2006 Report Share Posted June 14, 2006 ....Although I was not on your list, I am doing great. Five years on AP and no pain or other drugs. Came out of remission once and went back up to a higher dose. Went right back in remission and then back on a maintanance dose. I am grateful that the Minocin continues to work and did once get an email from an 85 year old man who had been on of Dr Browns patients. It was still working for him after 40 years!!! Please God, let me be like him!! Martha Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 14, 2006 Report Share Posted June 14, 2006 >I see some of the people posting on the two other sites I know of. what exactly are the other two sites? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 14, 2006 Report Share Posted June 14, 2006 The Roadback Foundation has a site...plug it into your browser. There is also a site _http://www.rheumaticsupport.net/_ (http://www.rheumaticsupport.net/) which is informative. I browse both of them occasionally but the email on this site is easy to keep up with and I tend to see anything new that someone sends. On the other hand all the information is helpful, and when one is struggling the more helping hands the better. If one candle brightens the darkness, think how much better three will be. Martha Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 14, 2006 Report Share Posted June 14, 2006 Gwen, I would quickly go back to format and request the Digest version instead of the individual emails. Some of the new ones here need the same amount of attention that we " oldies " got way back when. Life will be simpler for you, then! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 14, 2006 Report Share Posted June 14, 2006 thanks , . Not sure what you mean " go back to format " . How do I do that? Gwen Re: rheumatic group Gwen, I would quickly go back to format and request the Digest version instead of the individual emails. Some of the new ones here need the same amount of attention that we " oldies " got way back when. Life will be simpler for you, then! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 14, 2006 Report Share Posted June 14, 2006 GWEN, THIS IS A SIGHT FOR OTHERS TO GET INFORMATION ON THERE DISEASES, IF YOURS IS UNDER CONTROL OR YOU ARE MORE INFORMED? LOG OFF FOR AWHILE. OTHER NEW MEMBERS ARE TRYING TO HELP THEMSELVES. GOD-BLESS ROSE (OLD MEMBER BUT STILL TRYING TO UNDERSTAND). rheumatic group Just got back from a stint in hospital.What is with all the mail in the group all of a sudden? My mail box was full , just in the last few days. Not sure what to do about this---I really don't want to discontinue my involvement but I can't have this happen all the time. Gwen (old member) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 15, 2006 Report Share Posted June 15, 2006 Martha Do you have R.A.? I am 60, and have gone into remission after many years of pain. I did standard protocal for approx. 10 years and then approx 5 years of I.V. Clindamycin. Did you ever get deformities or joint replacements? I have had many. I do fear the return of the R.A. Right now, I take prednizone (4 mg.), celebrex 2x daily, ranitidine, and pain drugs as needed. Thanks, Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 15, 2006 Report Share Posted June 15, 2006 The IV'S are paid for if you have medicare. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 15, 2006 Report Share Posted June 15, 2006 Dear , Will you please elaborate on the 5 years of Clindamicin IVs? How many times a week did you go, etc. . . I have been doing the Clindamicin IVs for several months now and I had no idea it could take years (it's $75/IV)! kjdel1977@... wrote: Martha Do you have R.A.? I am 60, and have gone into remission after many years of pain. I did standard protocal for approx. 10 years and then approx 5 years of I.V. Clindamycin. Did you ever get deformities or joint replacements? I have had many. I do fear the return of the R.A. Right now, I take prednizone (4 mg.), celebrex 2x daily, ranitidine, and pain drugs as needed. Thanks, Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 15, 2006 Report Share Posted June 15, 2006 I did the IV's for 6 or 7 years. At first I did them once a week for 10 weeks and then a 5 day stretch of daily then back to the 10 weeks. I did that for a year. Later I did them 4 day stretches once a month and then the last year only a 4 day stretch when I noticed symptoms. I administered my own since I am a nurse so it was not as expensive as getting someone to do them. It was the best thing I did. cooky By the way if you have not read all of our biographys go to rheumatic.org/medhist.htm Re: rheumatic re: group Dear , Will you please elaborate on the 5 years of Clindamicin IVs? How many times a week did you go, etc. . . I have been doing the Clindamicin IVs for several months now and I had no idea it could take years (it's $75/IV)! kjdel1977@... wrote: Martha Do you have R.A.? I am 60, and have gone into remission after many years of pain. I did standard protocal for approx. 10 years and then approx 5 years of I.V. Clindamycin. Did you ever get deformities or joint replacements? I have had many. I do fear the return of the R.A. Right now, I take prednizone (4 mg.), celebrex 2x daily, ranitidine, and pain drugs as needed. Thanks, Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 15, 2006 Report Share Posted June 15, 2006 Oh, I don't have medicare. I am only 28 years old. Tooshooze@... wrote: The IV'S are paid for if you have medicare. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 16, 2006 Report Share Posted June 16, 2006 Could you tell me where you doctor at? I would sure be glad to have medicare pay for the IV's SKip Re: rheumatic re: group The IV'S are paid for if you have medicare. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 16, 2006 Report Share Posted June 16, 2006 Hi Gwen! Geoff here. You wrote: > Just got back from a stint in hospital.What is with all the mail in the > group all of a sudden? My mail box was full , just in the last few days. Rather than doing as Craig suggests, you might change your settings at Groups to get the digest rather than individual emails. That condenses the volume considerably. Geoff Acts 2:39 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 19, 2006 Report Share Posted June 19, 2006 www.rheumaticsupport.net is one. I don;t know the URL for the rfb. Re: rheumatic re: group >I see some of the people posting on the two other sites I know of. what exactly are the other two sites? Quote Link to comment Share on other sites More sharing options...
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