Guest guest Posted February 21, 2012 Report Share Posted February 21, 2012 Diane tell your friend not to waste her money, she will not get any benefit, I have tried them all, directly into the brain, into the blood, and slow release capsules every month for a year. > Hi everyone. > Has anyone had a stem cell transplant or know of anone with MS that has. What was the outcome and I would love to here your opinions on it. Someone I know is considering it and I wanted to know what other msers think. > Thank You. > Diane > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 23, 2012 Report Share Posted February 23, 2012 That is only one perspective.....I did stem cell therapy in Mexico where they took the stem cells out of the bone marrow in my leg and put them directly back into my body...and I had a HUGE benefit. All my symptoms went completely away after a few months. 2 years later little symptoms started to come back here and there, but nothing major. I am now on LDN to keep in that way. But if I ever had to do it again, I'd do it again in a heartbeat. ----- Re: Stem Cell Transplant Date: Tue, 21 Feb 2012 16:48:06 +0800 <!DOCTYPE HTML PUBLIC " -//W3C//DTD HTML 4.01//EN " " http://www.w3.org/TR/html4/strict.dtd " > Diane tell your friend not to waste her money, she will not get any benefit, I have tried them all, directly into the brain, into the blood, and slow release capsules every month for a year. > Hi everyone. > Has anyone had a stem cell transplant or know of anone with MS that has. What was the outcome and I would love to here your opinions on it. Someone I know is considering it and I wanted to know what other msers think. > Thank You. > Diane > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 23, 2012 Report Share Posted February 23, 2012 - What form of MS did you have going into the stem cell transplant? Does anyone know who performs that on pp with SPMS or PPMS? > Hi everyone. > Has anyone had a stem cell transplant or know of anone with MS that has. What was the outcome and I would love to here your opinions on it. Someone I know is considering it and I wanted to know what other msers think. > Thank You. > Diane > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 23, 2012 Report Share Posted February 23, 2012 That is fantastic to hear!! :)Congratulations on your treatment's success! 'What we do in life, echoes through eternity.' MARCUS AURELIUS (121 - 180 A.D.) To: mscured From: tazeeyore@... Date: Thu, 23 Feb 2012 13:05:51 +0000 Subject: Re: Stem Cell Transplant That is only one perspective.....I did stem cell therapy in Mexico where they took the stem cells out of the bone marrow in my leg and put them directly back into my body...and I had a HUGE benefit. All my symptoms went completely away after a few months. 2 years later little symptoms started to come back here and there, but nothing major. I am now on LDN to keep in that way. But if I ever had to do it again, I'd do it again in a heartbeat. ----- Re: Stem Cell Transplant Date: Tue, 21 Feb 2012 16:48:06 +0800 <!DOCTYPE HTML PUBLIC " -//W3C//DTD HTML 4.01//EN " " http://www.w3.org/TR/html4/strict.dtd " > Diane tell your friend not to waste her money, she will not get any benefit, I have tried them all, directly into the brain, into the blood, and slow release capsules every month for a year. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 23, 2012 Report Share Posted February 23, 2012 Hi , As far as the LDN, thanks to Dudley, I did not need a prescription. http://www.webspawner.com/users/howtoobtainldn/index.html Here is where you can buy it https://www.alldaychemist.com/search.php?search_query=Naltrexone+ and this is how you make it (per Dudley)... Once you have a supply of 50 mg Naltrexone tablets, you can convert them as needed to LDN. To do so, fill a graduated cylinder with 50 ml of distilled water (unlike tap or spring water, distilled water contains no impurities that could potentially react with and thus reduce Naltrexone's effectiveness). Pour the water from the graduate into a 4 oz amber glass jar with a tight-fitting lid. Then add a 50 mg Naltrexone tablet. The tablet will mostly dissolve in about five to ten minutes. Since not all of the tablet is soluble in water, instead of yielding a clear solution, the result will be a cloudy suspension. It must be shaken each time before use to evenly disperse all the undissolved particles. One ml of the (shaken) suspension will contain one mg of Naltrexone. You can use a graduated baby medicine dropper to measure out the dose you need. For greater accuracy, some people prefer to use a regular medicine dropper and add the LDN drop-by-drop into a 5 ml graduated cylinder. It is also possible to draw up fairly accurate doses using an oral dosage syringe. As far as the Stem Cell therapy, here is the e-mail address of the Dr. I saw doctor_andrade@..., when you e-mail him, let him know it was me who referred you (). Basically I went to Mexico for 1 week. They tested my blood and urine for all sorts of things, and based how to preceed with treatment from there. They gave me high doses of Vit. C and amino acids, a very small does of Chemo to regulate my immunity, and on the 3rd day took out the stem cells and immediately put them back in my body. By the 5th day I was able to go home. This is in Tijuana Mexico, just over the border, they put you up in a nice 4 star hotel which is only a block away from the clinic. Everyday they pick you up and bring you to the clinic, you basically spend the day there everyday, and then they bring you back to your hotel for the night. He has has great success with this treatment. At first my symptoms got a little worse, but then within a few months, every single symptom I had when completely gone. They did start to come back after a couple of years...but with that said, I went back to my normal lifestyle. I didn't modify my diet, I wasn't taking any supplements, I wasn't on LDN. Had I been doing any of those things, the symptoms may have never came back. The symptoms that did come back were very minor, not like they were before. I'd get a little tingling here and there, a little numbness here and there, and slight pain here and there, all of which would come and go. Most of the time, I still had no symptoms. But since I was experiencing this, I was afraid that eventually they would come back stronger, and that is why I got on LDN. Since being on LDN, a rarely get a symptom at all. When I do, it is one of those aboved mentioned and is very short lived. Hope this helps, feel free to e-mail back with any further questions. I will also send this to MScured in case it can help anyone else who may be interrested. ____________________________________________________________ 57 Year Old Looks 27 Local Woman Reveals Wrinkle Secret That Has Doctors Angry. http://thirdpartyoffers.juno.com/TGL3131/4f4668d9335dd16f501cst02vuc Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 23, 2012 Report Share Posted February 23, 2012 - so happy for you. Sounds encouraging for people with MS. How did you find out about this doctor? Any other info about this would be appreciated. Diane Subject: RE: Stem Cell Transplant To: mscured Date: Thursday, February 23, 2012, 10:25 AM  Hi , As far as the LDN, thanks to Dudley, I did not need a prescription. http://www.webspawner.com/users/howtoobtainldn/index.html Here is where you can buy it https://www.alldaychemist.com/search.php?search_query=Naltrexone+ and this is how you make it (per Dudley)... Once you have a supply of 50 mg Naltrexone tablets, you can convert them as needed to LDN. To do so, fill a graduated cylinder with 50 ml of distilled water (unlike tap or spring water, distilled water contains no impurities that could potentially react with and thus reduce Naltrexone's effectiveness). Pour the water from the graduate into a 4 oz amber glass jar with a tight-fitting lid. Then add a 50 mg Naltrexone tablet. The tablet will mostly dissolve in about five to ten minutes. Since not all of the tablet is soluble in water, instead of yielding a clear solution, the result will be a cloudy suspension. It must be shaken each time before use to evenly disperse all the undissolved particles. One ml of the (shaken) suspension will contain one mg of Naltrexone. You can use a graduated baby medicine dropper to measure out the dose you need. For greater accuracy, some people prefer to use a regular medicine dropper and add the LDN drop-by-drop into a 5 ml graduated cylinder. It is also possible to draw up fairly accurate doses using an oral dosage syringe. As far as the Stem Cell therapy, here is the e-mail address of the Dr. I saw doctor_andrade@..., when you e-mail him, let him know it was me who referred you (). Basically I went to Mexico for 1 week. They tested my blood and urine for all sorts of things, and based how to preceed with treatment from there. They gave me high doses of Vit. C and amino acids, a very small does of Chemo to regulate my immunity, and on the 3rd day took out the stem cells and ! immediately put them back in my body. By the 5th day I was able to go home. This is in Tijuana Mexico, just over the border, they put you up in a nice 4 star hotel which is only a block away from the clinic. Everyday they pick you up and bring you to the clinic, you basically spend the day there everyday, and then they bring you back to your hotel for the night. He has has great success with this treatment. At first my symptoms got a little worse, but then within a few months, every single symptom I had when completely gone. They did start to come back after a couple of years...but with that said, I went back to my normal lifestyle. I didn't modify my diet, I wasn't taking any supplements, I wasn't on LDN. Had I been doing any of those things, the symptoms may have never came back. The symptoms that did come back were very minor, not like they were before. I'd get a little tingling here and there, a little numbness here and there, and slight pain here and there, all of which would come and go. Most of the time, I still had no symptoms. But since I was experiencing this, I was afraid that eventually they would come back stronger, and that is why I got on LDN. Since being on LDN, a rarely get a symptom at all. When I do, it is one of those aboved mentioned and is very short lived. Hope this helps, feel free to e-mail back with any further questions. I will also send this to MScured in case it can help anyone else who may be interrested. __________________________________________________________ 57 Year Old Looks 27 Local Woman Reveals Wrinkle Secret That Has Doctors Angry. http://thirdpartyoffers.juno.com/TGL3131/4f4668d9335dd16f501cst02vuc Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 23, 2012 Report Share Posted February 23, 2012 I think one of my reasons for success, is that I went and did the treatment almost immediately after I was diagnosed with Relapse Remitting MS. Because I suspected it, I was already doing research on what I wanted to do. I started watching U-Tube videos on people who have done stem cell therapy and came across a guy (named ) who had this treatment done in Mexico, and even the doctor was in the video. His e-mail address was in the info for the u-tube video, so I e-mailed him to get doctor's info. That is how I found the doctor in Mexico. Overall it was a pleasant experience. Here was the original video I found... - This shows the doctor, and the guy was actually on the Montel show, which can be found on U-Tube as well. ----- Re: Stem Cell Transplant Date: Thu, 23 Feb 2012 05:41:27 -0800 (PST) <!DOCTYPE HTML PUBLIC " -//W3C//DTD HTML 4.01//EN " " http://www.w3.org/TR/html4/strict.dtd " > - What form of MS did you have going into the stem cell transplant? Does anyone know who performs that on pp with SPMS or PPMS? .. ____________________________________________________________ 53 Year Old Mom Looks 33 The Stunning Results of Her Wrinkle Trick Has Botox Doctors Worried http://thirdpartyoffers.juno.com/TGL3131/4f469409587491709b36st01vuc Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 23, 2012 Report Share Posted February 23, 2012 I forgot to mention that even though I had RRMS, he has treated people with both SPMS and PPMS, and even ALS with great results. The also treat cancer, and while I was there, people from the US whom their doctor's had given up hope on them with their cancer...have been cured at his clinic! Although they will use chemotherapy, they use it in moderation, along with high doses of vitamins, amino acids, etc...and have achieved great success with cancer. If I ever had cancer, I would not be treated in the US, I'd be going to his clinic. I do have the doctor's home and cell number as well if anyone was very serious about having this done. ----- Re: Stem Cell Transplant Date: Thu, 23 Feb 2012 05:41:27 -0800 (PST) <!DOCTYPE HTML PUBLIC " -//W3C//DTD HTML 4.01//EN " " http://www.w3.org/TR/html4/strict.dtd " > - What form of MS did you have going into the stem cell transplant? Does anyone know who performs that on pp with SPMS or PPMS? > Hi everyone. > Has anyone had a stem cell transplant or know of anone with MS that has. What was the outcome and I would love to here your opinions on it. Someone I know is considering it and I wanted to know what other msers think. > Thank You. > Diane > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 24, 2012 Report Share Posted February 24, 2012 Thanks so much -Something to look into~Diane  Subject: Re: Stem Cell Transplant To: mscured Date: Thursday, February 23, 2012, 1:30 PM  I think one of my reasons for success, is that I went and did the treatment almost immediately after I was diagnosed with Relapse Remitting MS. Because I suspected it, I was already doing research on what I wanted to do. I started watching U-Tube videos on people who have done stem cell therapy and came across a guy (named ) who had this treatment done in Mexico, and even the doctor was in the video. His e-mail address was in the info for the u-tube video, so I e-mailed him to get doctor's info. That is how I found the doctor in Mexico. Overall it was a pleasant experience. Here was the original video I found... - This shows the doctor, and the guy was actually on the Montel show, which can be found on U-Tube as well. ----- Re: Stem Cell Transplant Date: Thu, 23 Feb 2012 05:41:27 -0800 (PST) <!DOCTYPE HTML PUBLIC " -//W3C//DTD HTML 4.01//EN " " http://www.w3.org/TR/html4/strict.dtd " > - What form of MS did you have going into the stem cell transplant? Does anyone know who performs that on pp with SPMS or PPMS? .. __________________________________________________________ 53 Year Old Mom Looks 33 The Stunning Results of Her Wrinkle Trick Has Botox Doctors Worried http://thirdpartyoffers.juno.com/TGL3131/4f469409587491709b36st01vuc Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 25, 2012 Report Share Posted February 25, 2012 Thanks for sharring , i have always wondered if stem cells would help reverse the effects of MS. russ > > > Hi everyone. > > Has anyone had a stem cell transplant or know of anone with MS that has. What was the outcome and I would love to here your opinions on it. Someone I know is considering it and I wanted to know what other msers think. > > Thank You. > > Diane > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 21, 2012 Report Share Posted March 21, 2012 Diane, I went for fetal stem cell transplant therapy in Barbados about 5 years ago. I know I got the real thing based on the credentials of the doctors there. The main doctor had done stem cell treatment after Chernobyl in Russia with good results. That is where it was used for the first time based on what the Russian Dr. told us, and it was not published per the Russian Dr. He had been a Professor at a major University or Research Institute that had been studying stem cell research for many years. I believe this was in the Ukraine and was part of the work in helping people after the Chernobyl disaster as an experiment to see if it would help people. He said they had good results. The procedure I had was very expensive, $25,000 plus the trip expenses. I got what I would say was a face lift from the experience. It did not affect the progression of MS that I am dealing with. I could not afford more treatments. I believe that the research for nervous system disorders like MS has not been perfected yet or had not been perfected at that time. (My doctor who travels the world lecturing and has her finger on the pulse of what is going on, told me that stem cell and MS research has not gotten to a point that it is viable treatment yet.) I know for heart disease , the results have been phenomenal based on what the Russian Doctor told our family. He had stem cells used for his heart after a heart attack and had a great recovery. He looked great. I have not heard of research here in the US with MS. In fact, it seems like much of the research has been kept under wraps. There may be research in other countries. I understand that Singapore is where the leading research on stem cells is being done. I also believe that there is great possibility with stem cells, I just don't think it has been perfected yet. Johanna in San , CA. Hi everyone. Has anyone had a stem cell transplant or know of anyone with MS that has. What was the outcome and I would love to hear your opinions on it. Someone I know is considering it and I wanted to know what other msers think. Thank You. Diane Quote Link to comment Share on other sites More sharing options...
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