Guest guest Posted November 7, 2000 Report Share Posted November 7, 2000 Hello and group: I have been following Dr. ' research for some time and have communicated with him several times by email. He answers promptly and is very gracious. He is on the lecture circuit now, it appears, but I'm sure if anyone emailed him with questions about his theory he would respond. Rhonda ---------- > Date: Mon, 6 Nov 2000 11:13:34 +0100 > From: " D. Shaw " <.Shaw@...> > Subject: Re: Professor Jo ' web site > > Thanks for this. I note: > <quote> > Our conclusion is that autoantbodies are first made by chance but can set up a > vicious cycle so that they go on being produced in large amounts, causing > damage to body tissues. Removing the cells that make antibodies should break > this cycle. It is now possible to remove most of these cells safely and > effectively. Preliminary results are encouraging. > </quote> > > This is the bit I find worrying - the belief that the antibodies are made by > chance, and not because of infection by a bacteria or mycoplasma. This not > only flies in the face of other researchers (most noteably Dr. Ebringer, also > in London! - and has apparently identified the molecuar sequence on HLA-B27 > that is confused with that on K. pneumoniae for AS patients - pretty > conclusive that!) but suggests that antibiotic therapy is pointless, which > there are plenty here who will testify it is not. > > I am very concerned that this research is going to lead a lot of researchers > down the wrong track, especially now that it has received such wide publicity. > > Jo - I hope you're reading this! > > > >> Professor Jo ' web site, which discusses the RA treatment discussed >> in my previous posting, is at: http://www.ucl.ac.uk/~regfjxe/ >> >> -Dr. Todd- > > > ________________________________________________________________________ > ________________________________________________________________________ > > Message: 2 > Date: Mon, 6 Nov 2000 21:44:21 +0100 (CET) > From: and Chas Adlard <cadlard@...> > Subject: Re: IV Protocol > > > Hi Jeffery, > > Welcome to the group > > The IV protocol is based on the clinical experience of Dr. > McPherson Brown, a US rheumatologist who used this protocol for fifty > years. The basic protocol is described in question 2 of our FAQ at > rheumatic.org/faq.htm. Variations are made in each individual case > according to disease severity, whether other problems are also present > etc. > > Scleroderma patients usually need both antibiotics. A good pattern is to > start with a week of IVs, 300mg clindamycin or lincocin the first two > days, 600mg the second two days, 900mg the rest of the week. Then oral > minocycline is continued and a 900mg clindamycin IV is given once every > week, once every two weeks or once a month. > > Please let me know if you need more information and I'll try to help you, > Chris. > > > On Sat, 4 Nov 2000, Jeffery Abplanalp wrote: > >> I was diagnosed w/ scleroderma w/in the past year and began AP this past >> May. >> F., about a week ago you commented about Clindamycin IVs and >> mentioned the specific protocol that you are currently following. I'm >> interested in knowing how you arrived at that specific protocol. I'm >> struggling just a bit with frequency and dosage - what is generally accepted >> to be effective and what is not. Like with any med, I know there must be >> some variability from person to person. But surely there must be some >> insight amongst those who administer IVs as to what appears to be reasonably >> effective, or is it mostly trial and error? >> Thanks, >> Jeff >> >> _________________________________________________________________________ >> Get Your Private, Free E-mail from MSN Hotmail at http://www.hotmail.com. >> >> Share information about yourself, create your own public profile at >> http://profiles.msn.com. >> >> >> >> To unsubscribe, email: rheumatic-unsubscribeegroups >> >> > > > > > ________________________________________________________________________ > ________________________________________________________________________ > > Message: 3 > Date: Mon, 6 Nov 2000 11:23:52 +0100 > From: " D. Shaw " <.Shaw@...> > Subject: Re: Colitis connected w/arthritis? > > Hi > >> I've always felt this was probably an area in which the docs just don't know >> as much as they would like to let on, and am always interested in learning >> more. Do you have more references on Dr. Ebringer's work? > > http://www.kickas.org/mollecular_mimicry.shtml > > http://www.kickas.org/asdiet.shtml > > There is some stuff on ReA in these articles. > > Regards, > > > > ________________________________________________________________________ > ________________________________________________________________________ > > Message: 4 > Date: Mon, 06 Nov 2000 15:10:40 -0000 > From: john.downing@... > Subject: Anyone been to Dr. Anne Bacon? > > I am looking for an AP doctor in the Northern Virginia area > and have heard this name mentioned. Her office is in Winchester, > VA. Has anyone ever been to her. > > Thanks, > > > > ________________________________________________________________________ > ________________________________________________________________________ > > Message: 5 > Date: Mon, 06 Nov 2000 16:28:55 -0000 > From: " Mark Holmes " <mholmes@...> > Subject: PPA Warning-Women under 50 warning > > http://www.cnn.com/2000/HEALTH/11/06/ppa.warning.ap/ > > > > ________________________________________________________________________ > ________________________________________________________________________ > > Message: 6 > Date: Mon, 6 Nov 2000 11:45:50 EST > From: STKWINGUY@... > Subject: St. 's Wort Interaction with Drugs > >>>I wish I had a reference for this but I don't. There was some > discussion a while back about this and it could be that St. 's Wort > interacts with antibiotics in such a way as to reduce their effectiveness. I > immediately stopped taking it, because I don't want anything to interfere > with the AP. But I don't know if there is any proof for this... << > > Quoted from Consumer Reports On Health, June 2000 issue: > ..*. St 's wort can cause blood levels of a wide variety of prescription > drugs to plummet, with potentially dangerous results. > Researchers believe St 's wort affects drug metabolism by boosting > production of a key enzyme in the liver, speeding elimination of many common > drugs. Among the drugs probably affected: > Oral contraceptives; Statins; Beta-blockers; Calcium-channel blockers; > Digitalis; Theophylline; Warfarin (Coumadin); Certain antibiotics, notably > clarithromycin (Biaxin) and erythromycin (E-Mycin). > Moreover, St 's wort may interact in a different way with other > antidepressant medications, magnifying their intended effects as well as > their side effects, such as agitation and confusion as well as increased > blood pressure and heart rate. > And the herbal may increase sensitivity to light, a side effect that may be > compounded when it's taken with with drugs that cause the same problem, such > as tretinoin (Renova, Retin-A) and the antibiotics doxycycline (Vibramycin) > and tetracycline (Achromycin). > If your taking a prescription drug and want to try St 's wort, ask your > doctor whether the herbal is likely to interact with the drug. > And if you're already taking St 's wort plus a prescription drug, don't > STOP the herbal until you talk with your doctor, who can check to make sure > the blood level of the drug does not RISE precipitiously when the herbal is > discontinued. > <End of quote> > > > ________________________________________________________________________ > ________________________________________________________________________ > > Message: 7 > Date: Mon, 06 Nov 2000 10:07:20 -0700 > From: Gwen Armstrong <armstrog@...> > Subject: more letters like this might get action > > http://www.medscape.com/Medscape/GeneralMedicine/journal/2000/v02.n06/mgm110 3.gibs/mg > m1103.gibs.html > > > > ________________________________________________________________________ > ________________________________________________________________________ > > Message: 8 > Date: Mon, 6 Nov 2000 12:07:52 -0800 > From: " Liz G. " <pioneer@...> > Subject: Pamidronate and pred-induced osteoporosis--article > > http://www.docguide.com/news/content.nsf/news/75B09BCB4BFAC9758525698B007029 > F3?OpenDocument & id=4818A9BB262494A6852568C500627E56 & c=Arthritis%20Other & coun > t=10 > > Guess you'll have to copy and paste this back together.... > Article: > ACR: Pamidronate Prevents Glucocorticod-Induced Osteoporosis > > > > > > ________________________________________________________________________ > ________________________________________________________________________ > > Message: 9 > Date: Mon, 06 Nov 2000 15:17:21 -0600 > From: Probert <elbows@...> > Subject: Re: Re: Colitis connected w/arthritis? > > on 11/6/00 4:23 AM, D. Shaw at .Shaw@... wrote: > >> Hi >> >>> I've always felt this was probably an area in which the docs just don't know >>> as much as they would like to let on, and am always interested in learning >>> more. Do you have more references on Dr. Ebringer's work? >> >> http://www.kickas.org/mollecular_mimicry.shtml >> >> http://www.kickas.org/asdiet.shtml >> >> There is some stuff on ReA in these articles. >> >> Regards, >> > > Hi , as you probably know, I have read that material. I would like to > encourage anyone who disputes that or I could have reactive arthritis > to re-read it, as Dr Ebringer definitely does not state that HLA-B27 > positive status is necessary for a diagnosis of ReA. > > It seems most of my posts anymore are to remind folks who have > over-simplified the work of Ebringer and others that they are indeed > over-simplifying. > > What is stated in the above references is that approximately 70% of people > with the ReA diagnosis are HLA-B27 positive. This leaves a full 30% who are > not, including me. I have had rheumatologist state that in women with > post-dysenteric ReA, there is NO correlation with HLA-B27 status. Dr > Ebringer states that we probably have closely related tissue types. I > believe this is the area in which there is still more to be discovered. > > I have had uveitis, which is considered as important a factor in the > diagnosis as HLA-B27 status, and another indicator for more severe or > prolonged disease activity. > > Both and I have been on the list a while now, and have been through > this several times. I feel Dr. Franco is more qualified to make 's > diagnosis than list members. Just want to remind folks that we are mostly > amateurs here, and need to be careful about over-simplifying what we do > know, or generalizing one's experience to others inappropriately. > > Jean > > > > ________________________________________________________________________ > ________________________________________________________________________ > > Message: 10 > Date: Mon, 6 Nov 2000 18:16:30 EST > From: Tomlinkara@... > Subject: Latest Venture > > Hi everyone, > Thought you may be interested in following my story.Have RA and been on AP > since Apr 97.Made an amazing recovery for 1 and 1/2 years then got stuck.Have > been in a plateau since Aug 98.Sed rate hovers around 40 (+ or- 5) and have > persistent pain in my hands and wrists.(The last symptom to go away).So am > seeing Dr .On Fri I had an injection of Vit and min.Today I had an IV > treatment of hydrogen peroxide.Tomorrow I have chelation therapy with DMPS.I > also go and have a sauna following treatments ( to get rid of toxins) then > come home and drink tons of water.IV Clindamycin is also a > possibility.Anyway-so far no change .I can't tell you how much of a relief it > would be to be able to use my hands without pain. > Hugs, > Lin > PS I also have a positive ASO titre that won't respond to treatment.Maybe > this will help > > > ________________________________________________________________________ > ________________________________________________________________________ > > Message: 11 > Date: Mon, 06 Nov 2000 17:42:36 -0600 > From: Snooks <emsnooks@...> > Subject: Re: Anyone been to Dr. Anne Bacon? > > Our list shows the following address for Dr. Bacon: > > Anne Bacon, M.D. - Rheumatologist > Arthritis Specialists of Winchester > 1730 Amherst St. > Winchester, VA 22601 > > It's my understanding she does both oral and IV therapy. > 540-667-6232 > > Ethel > john.downing@... wrote: >> >> I am looking for an AP doctor in the Northern Virginia area >> and have heard this name mentioned. Her office is in Winchester, >> VA. Has anyone ever been to her. >> >> Thanks, >> >> >> To unsubscribe, email: rheumatic-unsubscribeegroups > > > ________________________________________________________________________ > ________________________________________________________________________ > > Message: 12 > Date: Tue, 07 Nov 2000 00:17:15 -0000 > From: marisa@... > Subject: PA Webcast Transcript is Available! > > Hello! > > I just wanted to let you all know that the transcript for the > HealthTalk Interactive psoriatic arthritis webcast, > entitled " Understanding Psoriatic Arthritis: Hope Through Knowledge > and New Treatments, " is up on our site at > http://www.healthtalk.com/rain/101700/replay.html. Please take a > moment to check it out and let me know if you have any questions or > comments! > > We also have other content on rheumatoid arthritis. Visit our > Rheumatoid Arthritis Information Network (RAIN) at > http://www.healthtalk.com/rain/rainindex.html. > > Warmest Regards, > > Marisa > > > > ________________________________________________________________________ > ________________________________________________________________________ > > Message: 13 > Date: Tue, 7 Nov 2000 01:04:41 GMT > From: " Adlard " <cadlard@...> > Subject: Re: Latest Venture > > Hi Lin, > > I'd be interested to know if chelation helps you - Janene is also considering > this option to ease stiffness. I had an email from a Dr. Mezo saying that the > stiffness which remains is caused by calcium deposits in the joints and that > chelation eliminates these deposits. > > Looking forward to hearing from you, > Chris. > >>Hi everyone, >>Thought you may be interested in following my story.Have RA and been on AP > >>since Apr 97.Made an amazing recovery for 1 and 1/2 years then got stuck.Have > >>been in a plateau since Aug 98.Sed rate hovers around 40 (+ or- 5) and have > >>persistent pain in my hands and wrists.(The last symptom to go away).So am > >>seeing Dr .On Fri I had an injection of Vit and min.Today I had an IV > >>treatment of hydrogen peroxide.Tomorrow I have chelation therapy with DMPS.I > >>also go and have a sauna following treatments ( to get rid of toxins) then > >>come home and drink tons of water.IV Clindamycin is also a >>possibility.Anyway-so far no change .I can't tell you how much of a relief > it >>would be to be able to use my hands without pain. >>Hugs, >>Lin >>PS I also have a positive ASO titre that won't respond to treatment.Maybe > >>this will help >> >> >>To unsubscribe, email: rheumatic-unsubscribeegroups >> >> >> > > > > ________________________________________________________________________ > ________________________________________________________________________ > > Message: 14 > Date: Tue, 07 Nov 2000 04:24:57 -0000 > From: " Mark Holmes " <mholmes@...> > Subject: Allergy sufferers take heed > > Be careful when taking herbs if you have allergies. Some info here > you might not have known. I realize that this group is a hotbed for > alternative medicine, but like regular drugs, herbal meds are not > always a safe alternative. > > http://www.msnbc.com/news/485764.asp?0nm=-19L > > Mark > SW VA > http://mark_holmes.tripod.com > > > > > > > ________________________________________________________________________ > ________________________________________________________________________ > > Message: 15 > Date: Tue, 7 Nov 2000 00:27:03 EST > From: Careabxs@... > Subject: Re: St. 's Wort Interaction with Drugs > > Thank you so much for the info from Consumer's Reports on SJW Your > response plus those of many other people have me taking a second look at > using this. I am on 12 different prescription medicines, including a calcium > channel blocker so I don't want to make things worse for myself! I just wish > that the two rheumy's I saw would have cautioned me about this! > Thanks again > Carol E from NY > > > > [This message contained attachments] > > > > ________________________________________________________________________ > ________________________________________________________________________ > > Message: 16 > Date: Tue, 07 Nov 2000 06:03:59 -0000 > From: " Borland " <lborland@...> > Subject: Re: Colitis > > Hi , > It's great to hear you're getting good results from HBOT. 20 years > is a long time to put up with anything. I think the colitis is > related to the arthritis. From everything I've heard about leaky gut > syndrom it sounds like that's the mechanism for infection entering > the bloodstream where it causes systemic problems. Anything that > causes inflammation of the intestinal walls also causes increased > permeabilty. The walls of the intestines, though they appear solid, > are actually like a very fine sive that allows only the tiniest > molecules to get through. Anything larger will cause an immediate > attack by the immune system. With LGS, plenty of the large stuff > gets through. The " molecular mimicry " causes antibodies fighting > these large molecules (including parts or organisms that are > molecular in size) to then attack healthy tissue. I just learned > recently that certain immunizations worked on that principle. For > example, with a gammaglobulin shot they inject you with something > harmless that is so similar to the hepatitus virus that you form > antibodies that will attack the hepatitus too. That's a type of > molecular mimicry that works to our benefit. > > > > >> > > According to Dr. Alan Ebringer ReA and AS are associated with >> HLA-B27 and RA >> > > is associated with HLA-DR4/DR1. I didn't want you to think I > was >> referring to >> > > reactive arthritis when I used RA. Reactive Arthritis is a >> classification >> > > that includes Reiter's Syndrom and a host of other infections > that >> cause joint >> > > inflammation. It's much easier to get your rheumatologist to >> treat with >> > > antibiotics when you have ReA because they recognize that there > is >> an >> > > infection causing the symptoms. The trouble is that most of > them >> don't look >> > > for ReA unless you show other symptoms of infection besides just >> joint >> > > inflammation. However, sometimes that's the only symptom that >> shows. >> > >> > Hi >> > >> > I find your comments on HLA-B27 interesting. My diagnosis is >> reactive >> > arthritis, but I am HLA-B27 negative. My rheumatologist made the >> diagnosis >> > based upon characteristic enthesopathy of heels, hips, etc, and >> uveitis. Two >> > other rheumatologists have confirmed this diagnosis. The last one >> said in >> > women with post-dysenteric ReA, there is NO correlation between >> arthritis >> > and HLA-B27 status. All the rheumatologists I've spoken with felt >> uveitis >> > was in my case as important to the diagnosis as HLA-B27 status. >> > >> > My first rheumatologist said he suspected I would be positive for >> > HLA-DR4/DR1, but felt the expense of the tests was not justified > in >> the >> > light of other positive indicators. >> > >> > I've always felt this was probably an area in which the docs just >> don't know >> > as much as they would like to let on, and am always interested in >> learning >> > more. Do you have more references on Dr. Ebringer's work? >> > >> > For the record, I have had arthritis for 13 years, have had a good >> response >> > to 14 months of minocycline, but am still hoping for more >> improvement. >> > >> > TIA >> > >> > Jean > > > > ________________________________________________________________________ > ________________________________________________________________________ > > Message: 21 > Date: 7 Nov 2000 08:10:06 -0000 > From: rheumaticegroups > Subject: Poll results for rheumatic > > > The following rheumatic poll is now closed. Here are the > final results: > > > POLL QUESTION: When new members join and/or old ones > unsubcribe, it is hard to keep track of > everyone's illnessess. To get a better > understanding of the > diseases of this group, please indicate > below the condition (s) that you are > currently afflicted with. > > CHOICES AND RESULTS > - Lupus, 0 votes, 0.00% > - Reactive Arthritis, 0 votes, 0.00% > - Rheumatoid Arthritis, 1 votes, 20.00% > - Sjogren's Diesease, 0 votes, 0.00% > - Scleroderma, 2 votes, 40.00% > - Polymyositis, 0 votes, 0.00% > - Dermatomyositis, 0 votes, 0.00% > - Reiter's Syndrome, 0 votes, 0.00% > - Ankylosing Spondylitis, 1 votes, 20.00% > - Psoriatic Arthritis, 1 votes, 20.00% > - Fibromyalgia, 0 votes, 0.00% > > INDIVIDUAL VOTES > - Lupus > - Reactive Arthritis > - Rheumatoid Arthritis > - asolomon@... > - Sjogren's Diesease > - Scleroderma > - RTC@... > - lcmedit@... > - Polymyositis > - Dermatomyositis > - Reiter's Syndrome > - Ankylosing Spondylitis > - .Shaw@... > - Psoriatic Arthritis > - john.downing@... > - Fibromyalgia > > > For more information about this group, please visit > rheumatic > > For help with eGroups, please visit > help > > > > > > > > ________________________________________________________________________ > ________________________________________________________________________ > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 23, 2001 Report Share Posted April 23, 2001 'oxyplus ' wrote: ==== - OxyPLUS is an unmoderated e-ring dealing with oxidative therapies, and other alternative self-help subjects. - - THERE IS NO MEDICAL ADVICE HERE! - - This list is the 1st Amendment in action. The things you will find here are for information and research purposes only. We are people sharing information we believe in. If you act on ideas found here, you do so at your own risk. Self-help requires intelligence, common sense, and the ability to take responsibility ...' > Take a look to the attachment. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 17, 2001 Report Share Posted August 17, 2001 Copy all, Gretchen! Thank you for the reminder. He has already paid the ultimate price. --------------- MODERATOR NOTE: One error I need to correct is that Steve's parents do speak English, but it is not their native language. His Mother's english is reported to be more fluent than his Dad's. Gretchen --------------- Date: Thu, 16 Aug 2001 20:28:01 -0000 From: anna_nim@... Subject: Re: Update information for September's Event >> 4) We are having a balloon launch in memory of all those that have been effected from the vaccine. >> When you launch the balloons, be sure to send up some for those who died. The name of Steve Suk needs to be added. He died at Walter this summer. In the end, he was bleeding through his pores, before his skin began falling off. DoD may not be heavily involved in 'dammage control' in his case, Steve was Korean, and his parents don't speak English. They aren't likely to connect with the vaccine activists any time soon. And I'm betting he won't be found listed in with those who had 'reactions' He and his family were discouraged from making the connection to the vaccine. Gretchen List owner ________________________________________________________________________ ________________________________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 11, 2002 Report Share Posted March 11, 2002 Hi All, I am joining the HB Group today! I has said I was joining last week but not only missed that but failed miserably and ate ice cream and potato chips for the first time in 3 years! EEEH GAD!! Also, you sent me a plan to get rid of cellulite a while back and I have misplaced it - how did it go? Thanks in advance for any assistance you can give me! Love and Laughter [and fitness and health] to all! Cj Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 27, 2005 Report Share Posted March 27, 2005 Dear Carol, I have made the decision to have revision sugery in June. I, like you, hadn't realized there was such a procedure until recently. I am still in reasonable shape, but I am getting progressively worse. I saw my original surgeon at Stanford Hospital and then saw Dr. Serena Hu, at UCSF. The Spine Center at UCSF is the place to go for this type of condition. There is also another doctor, Dr. Berven. Both he and Dr. Hu deal with revisions on a regular basis. There are only a handful of doctors in the country that specialize in revisions, and these two are in this group. Both doctors I saw said I have flat back syndrome and will need to have surgery. I can wait five years or so to do it. I decided to go for it now because I am in the best shape to handle recovery, I have good health insurance, and why obsess and be in pain for any longer than I have to. Neither doctor told me I would have to wait until I was in more pain or more disabled. I think that is counter productive considering the level of recovery needed to pull through this, both mentally and physically. Dr. Hu also said that women who have been through menopause generally tend to have poorer recoveries than premenopausal women. This is also another factor for me because I am osteopenic (almost osteoporotic) and I want my bone to fuse. If you decide to get an appointment with Dr. Hu be prepared to wait a month or two; she gets booked up fast. Good luck with all this. It's been an eventful few months for me learning about all of this and make such big decisions. Jenni Gates Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 29, 2005 Report Share Posted March 29, 2005 Thank you for the info.I am printing this out for future reference. As I said previously, I was not aware of HARMS. And as others have said, I'm sure very few if any Orthopedic Doctors are either. That's part of the reason why I've always felt like a freak. Everyone minimizes my pain and uncomfortableness. I know it's not in my head. I know it's a waste to go to my GP unless only for pain med's. So, I guess I'll slowly start my search. I will appreciate a lot of prayer. All this will have to come about in the right time, and right now it doesn't seem like the time. I have a daughter graduating from High School in June, so we'll we busy with that and college starting in the fall. Thank you everyone for your thoughts. Carol V. > > Dear Carol, > > I have made the decision to have revision sugery in June. I, like you, hadn't realized there was such a procedure until recently. I am still in reasonable shape, but I am getting progressively worse. I saw my original surgeon at Stanford Hospital and then saw Dr. Serena Hu, at UCSF. The Spine Center at UCSF is the place to go for this type of condition. There is also another doctor, Dr. Berven. Both he and Dr. Hu deal with revisions on a regular basis. There are only a handful of doctors in the country that specialize in revisions, and these two are in this group. Both doctors I saw said I have flat back syndrome and will need to have surgery. I can wait five years or so to do it. I decided to go for it now because I am in the best shape to handle recovery, I have good health insurance, and why obsess and be in pain for any longer than I have to. Neither doctor told me I would have to wait until I was in more pain or more disabled. I think that is counter productive > considering the level of recovery needed to pull through this, both mentally and physically. Dr. Hu also said that women who have been through menopause generally tend to have poorer recoveries than premenopausal women. This is also another factor for me because I am osteopenic (almost osteoporotic) and I want my bone to fuse. If you decide to get an appointment with Dr. Hu be prepared to wait a month or two; she gets booked up fast. Good luck with all this. It's been an eventful few months for me learning about all of this and make such big decisions. > > Jenni Gates Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 31, 2005 Report Share Posted March 31, 2005 Carol V. My name is Carole, and I imagine you are about the age of my own daughter. Please do not think of yourself the way you described. Didn't you produce a wonderful young woman? Aren't there other places in life that you can be so proud of? You know, you did not do anything to anyone. You were given a special place in life, just like I was. There are just so many of us out here! I am so glad that you found this site and am pretty sure you will be hearing from the moderator () too! Please hang in there. There are several online groups that have really kept my head " above water " for some time now! Welcome! Carole M. (the elder) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 10, 2008 Report Share Posted May 10, 2008 Hello Amit, this is praveen, i am a software engineer, was working for a MNC in France, due to a illness, i need to return india in 2003, for almost 2 years i was under treatment in SGPGI lucknow, still i am unable to walk, i move with the help of a walker, but the things are improving, and i am very positive that i will be able to walk soon on my own, kind words at this forum make me happy and encourage me. thanks praveen. Hello every body.I'm new to this group and would like to represent myself. My name is Dror I'm 45 years old from North Hollywood of beautifulCalifornia, Positive thinking is to my opinion by the root of goodsuccess in life and well being, I'm very glad to find this group andlooking forward to meet you guys and to run a prolific discussingwith you concern. Even though I do not really meditate these days I do Yoga threetime a week and I love it. Any one of you have some experiencewith Yoga? Have a wonderful day.Dror________________________________Be a better friend, newshound, and know-it-all with Mobile. Try it now. __________________________________________________________Be a better friend, newshound, and know-it-all with Mobile. Try it now. http://mobile./;_ylt=Ahu06i62sR8HDtDypao8Wcj9tAcJ Back to top Reply to sender | Reply to group | Reply via web post Messages in this topic (2) 2. Motivational Quote of the Day!~ [10 May 2008] Posted by: "Golden Inspirations" contactus@... golden.inspirations Sat May 10, 2008 3:45 am (PDT) *"Do not wait to strike till the iron is hot;but make it hot by striking."- B. Sprague <http://www.myeverydaypage.com/>** **Forward it to all your friends and make their day.**brought to you by:MyEverydayPage.com <http://www.myeverydaypage.com>** ** **In Association with:*[image: cid:image001.jpg01C8B1D1 (DOT) DA422BB0]<http://www.goldeninspiration.com/>*www.GoldenInspiration.com* Back to top Reply to sender | Reply to group | Reply via web post Messages in this topic (1) Recent Activity 22 New MembersVisit Your Group Health Memory Loss Are you at risk for Alzheimers? Meditation and Lovingkindness A Group to share and learn. Weight Loss Group on Get support and make friends online. Need to Reply? Click one of the "Reply" links to respond to a specific message in the Daily Digest. Create New Topic | Visit Your Group on the Web Messages | Files | Photos | Links | Database | Polls | Members | Calendar "Every day in every way,I'm getting better,better,better & better." Change settings via the Web ( ID required) Change settings via email: Switch delivery to Individual | Switch format to Traditional Visit Your Group | Terms of Use | Unsubscribe Quote Link to comment Share on other sites More sharing options...
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