Guest guest Posted April 7, 2006 Report Share Posted April 7, 2006 Hi , Welcome to our group! I think you will find what you are looking for here. There are wonderful people and good information and plenty of support. I might add there is hope with LDN. At least this is what I have found. I only started LDN a couple of weeks ago. I have tried all the crab drugs. They didn't help me and the side effects were awful. I cannot speak for you, but they were not worth it for me. LDN is safer and you are right, those needles were a drag. I am fortunate because I have a compounding pharmacy right near my home. I also have a really cool doctor who told me about LDN. It may not be as easy for some others as has been for me. I really do feel blessed. I am happy and hopeful. Pam Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 7, 2006 Report Share Posted April 7, 2006 > > Hi everyone, > I have just found out about LDN and didn't realize there was a pill > form that could maybe help my ms. I'm 44 yrs old and I was dx with > rrms in 2001. I just discovered all the testimonials and got very > hopeful and excited. > I've made an appointment with my GP for a prescription and hope I > have as much success as everyone I have read about. I also struggle > with numb & tingling hands, both my legs feel like a new born colt > trying to stand and have the bathroom habits of a 2 year old who has > had to much juice to drink. I have to joke a little it helps to > keep me going. I have also just started feeling the effects of > fatique, wow, talk about dragging you down, no energy whatsoever. I > use to walk 5km a day and lead a fairly active life, I feel so > robbed and defeated so I'm hoping I will have good luck with LDN > just a little quality of life returned to me would be great! My > neur. also wanted me to start the CRAB drugs and I said I wasn't > ready for that, I hate the thought of needles and all the side > effects they could give me. I guess that is why LDN is so appealing > because everyone is saying there are very little side effects. > Looking forward to meeting new friends online and what LDN will do > for me and hopefully I'll be able to help someone else. Bye for now > I'll keep you posted, from Calgary, Alberta Canada > ======== Welcome , You may want to look over my LDN forum and information center. The link to it is below. Just ignore the google ads at the top. No pop-ups there. Low Dose Naltrexone Forum - Home http://ldn.proboards3.com/index.cgi? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 7, 2006 Report Share Posted April 7, 2006 Hi , Would you like me to send you a copy of the " welcome e-mail " for LDN? Just let me know and I will send it right out. Kind regards Aletha [low dose naltrexone] Hopeful new ms member > Hi everyone, > I have just found out about LDN and didn't realize there was a pill > form that could maybe help my ms. I'm 44 yrs old and I was dx with > rrms in 2001. I just discovered all the testimonials and got very > hopeful and excited. > I've made an appointment with my GP for a prescription and hope I > have as much success as everyone I have read about. I also struggle > with numb & tingling hands, both my legs feel like a new born colt > trying to stand and have the bathroom habits of a 2 year old who has > had to much juice to drink. I have to joke a little it helps to > keep me going. I have also just started feeling the effects of > fatique, wow, talk about dragging you down, no energy whatsoever. I > use to walk 5km a day and lead a fairly active life, I feel so > robbed and defeated so I'm hoping I will have good luck with LDN > just a little quality of life returned to me would be great! My > neur. also wanted me to start the CRAB drugs and I said I wasn't > ready for that, I hate the thought of needles and all the side > effects they could give me. I guess that is why LDN is so appealing > because everyone is saying there are very little side effects. > Looking forward to meeting new friends online and what LDN will do > for me and hopefully I'll be able to help someone else. Bye for now > I'll keep you posted, from Calgary, Alberta Canada > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 8, 2006 Report Share Posted April 8, 2006 Hey Calgary, I am from Edmonton and everyone here says LDN don't exist in Canada. My friend with MS as well has been looking high and low for information but I'm more into doing things like this, joining this group. I am 46 and got my diagnose in 1997. I use to have symptoms like you too, then last year, I went to a Doctor Sandhar in Edmonton, he did a Blood Print on me, and now all those symptoms are gone. I almost went on Copexone too, but after the MS Specialists and Neurologists were blown away by my improvement so Copaxone can wait. But I would like to get more Canadian Information on why both of us, that have some of the same doctors, try keep us from knowing or even testing LDN out. (And, if you want to know more , since you are around the corner from my City, to let me know. Okay? Let me know what happens. Please. ) helpforms <helpforms@...> wrote: Hi everyone,I have just found out about LDN and didn't realize there was a pill form that could maybe help my ms. I'm 44 yrs old and I was dx with rrms in 2001. I just discovered all the testimonials and got very hopeful and excited.I've made an appointment with my GP for a prescription and hope I have as much success as everyone I have read about. I also struggle with numb & tingling hands, both my legs feel like a new born colt trying to stand and have the bathroom habits of a 2 year old who has had to much juice to drink. I have to joke a little it helps to keep me going. I have also just started feeling the effects of fatique, wow, talk about dragging you down, no energy whatsoever. I use to walk 5km a day and lead a fairly active life, I feel so robbed and defeated so I'm hoping I will have good luck with LDN just a little quality of life returned to me would be great! My neur. also wanted me to start the CRAB drugs and I said I wasn't ready for that, I hate the thought of needles and all the side effects they could give me. I guess that is why LDN is so appealing because everyone is saying there are very little side effects. Looking forward to meeting new friends online and what LDN will do for me and hopefully I'll be able to help someone else. Bye for nowI'll keep you posted, from Calgary, Alberta Canada Make free worldwide PC-to-PC calls. Try the new Canada Messenger with Voice Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 8, 2006 Report Share Posted April 8, 2006 Hi , Like you, I’m on a mission to find out as much as I can about LDN and how I will overcome any obstacles on obtaining this drug in Alberta. I’m going to see my GP in the middle of April and I’m hopeful she will give me a prescription as of this moment I’m just beginning this quest and I will keep you and others informed as to how I make out. Can you tell me what is a blood print? I’m not understanding what has helped your symptoms, are you on LDN? If so, did you get it from your GP and can you buy it in Alberta? Nice to know I have someone in this corner of the world to relate to our same concerns. from Calgary From: low dose naltrexone [mailto:low dose naltrexone ] On Behalf Of Luik Sent: Saturday, April 08, 2006 6:46 AM To: low dose naltrexone ; helpforms@... Subject: Re: [low dose naltrexone] Hopeful new ms member Hey Calgary, I am from Edmonton and everyone here says LDN don't exist in Canada. My friend with MS as well has been looking high and low for information but I'm more into doing things like this, joining this group. I am 46 and got my diagnose in 1997. I use to have symptoms like you too, then last year, I went to a Doctor Sandhar in Edmonton, he did a Blood Print on me, and now all those symptoms are gone. I almost went on Copexone too, but after the MS Specialists and Neurologists were blown away by my improvement so Copaxone can wait. But I would like to get more Canadian Information on why both of us, that have some of the same doctors, try keep us from knowing or even testing LDN out. (And, if you want to know more , since you are around the corner from my City, to let me know. Okay? Let me know what happens. Please. ) helpforms <helpforms@...> wrote: Hi everyone, I have just found out about LDN and didn't realize there was a pill form that could maybe help my ms. I'm 44 yrs old and I was dx with rrms in 2001. I just discovered all the testimonials and got very hopeful and excited. I've made an appointment with my GP for a prescription and hope I have as much success as everyone I have read about. I also struggle with numb & tingling hands, both my legs feel like a new born colt trying to stand and have the bathroom habits of a 2 year old who has had to much juice to drink. I have to joke a little it helps to keep me going. I have also just started feeling the effects of fatique, wow, talk about dragging you down, no energy whatsoever. I use to walk 5km a day and lead a fairly active life, I feel so robbed and defeated so I'm hoping I will have good luck with LDN just a little quality of life returned to me would be great! My neur. also wanted me to start the CRAB drugs and I said I wasn't ready for that, I hate the thought of needles and all the side effects they could give me. I guess that is why LDN is so appealing because everyone is saying there are very little side effects. Looking forward to meeting new friends online and what LDN will do for me and hopefully I'll be able to help someone else. Bye for now I'll keep you posted, from Calgary, Alberta Canada Make free worldwide PC-to-PC calls. Try the new Canada Messenger with Voice Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 8, 2006 Report Share Posted April 8, 2006 , Go to www.copingandprevailing.com If you cannot afford to pay for the book send me your mailing address and I will send it to you. Regards, Tom [low dose naltrexone] Hopeful new ms member > Hi everyone, > I have just found out about LDN and didn't realize there was a pill > form that could maybe help my ms. I'm 44 yrs old and I was dx with > rrms in 2001. I just discovered all the testimonials and got very > hopeful and excited. > I've made an appointment with my GP for a prescription and hope I > have as much success as everyone I have read about. I also struggle > with numb & tingling hands, both my legs feel like a new born colt > trying to stand and have the bathroom habits of a 2 year old who has > had to much juice to drink. I have to joke a little it helps to > keep me going. I have also just started feeling the effects of > fatique, wow, talk about dragging you down, no energy whatsoever. I > use to walk 5km a day and lead a fairly active life, I feel so > robbed and defeated so I'm hoping I will have good luck with LDN > just a little quality of life returned to me would be great! My > neur. also wanted me to start the CRAB drugs and I said I wasn't > ready for that, I hate the thought of needles and all the side > effects they could give me. I guess that is why LDN is so appealing > because everyone is saying there are very little side effects. > Looking forward to meeting new friends online and what LDN will do > for me and hopefully I'll be able to help someone else. Bye for now > I'll keep you posted, from Calgary, Alberta Canada > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 8, 2006 Report Share Posted April 8, 2006 Hello , You actually are getting better luck than I was when I was in Edmonton for over 2 years looking into this. My friend actually got me HOOKED onto finding more on Naltrexone when she kept on passing me information on it. When I went back to Milan, Italy where my husband refuses to budge from due to work, I got serious to find out where in Europe as well. I did a Blood Print and my husband immediately saw a difference in me. I was having mood swings, was wobbly, tired, was forgetful, or had memory problems, dropped things, had everything from dizziness, to insomnia, swollen tender joints, sporatic digestive issues and more. Then, another friend of mine suggested to see Doctor Sandhar, I thought it was the same that helped my little girl through a horrid sickness so said yes, but I discovered it was only the student of. I've learned so much since then, thanks to Doctor Sandhar. My husband also wants to do a Blood Print for himself, and my little girl needs to do one also. But, before I actually did the blood print, I wanted to know what I was getting into so followed him and the people he was helping since I knew a few. They all were better after a short time, so I thought, with not me with my ms, anything is better than... But again, my husband immediately saw a huge difference in me after I did my Blood Print and am following though this thanks to Doctor Sandhar in Edmonton, Alberta. His phone number is (780) 439-6907 and he could send you out information on the Blood Print. It analyses your blood on intollerances of all sort and kind but its done in the USA under strickt hygenic conditions. So it costs and is not covered by the Health Care in Canada and sort of like a Mineralgram test that takes a gram of your hair and analyses it from the root which tell us all about our bodies, allergies and ills. I did that one years ago and my thyroid issue showed up after I'd been trying to tell doctors I had it for years, but it never came up, but naturally, Hashimotos thyroid is extreemly hard to detect. A regular GP will either doubt it or send you off to do scratch tests for all sorts of allergies, but I can testify that none of the ones I've ever done ever came up so close to being me the way I now know of my body to be. . I am not on LDN, although both and I would like to try this, the specialists in MS and neurology, we now both have, had tried to convince me to go onto Copexone, but instead, I did that Blood Print - blood extracted and sent to a specialized clinic in the States. The website is www.BetterHealthUSA.com the toll free number is (800)231-9197. But going through a doctor like Doctor Sandhar actually helps your body to prepare for going through what you will go through. I was completely detoxed from numerous things before doing it. My husband didn't see me for numerous months while I went on it, but he noticed I was changing all the time. But again, the doctors I've had, are stumped into being either amazed or very quiet about the whole deal other than still trying to set me up with a psychogist to analyse my depression, and that seems to have disapaited all together, thank God. Now, with the same doctors tried to get her to do some trial without going into much detail so she said no, and is again, is trying to get her GP to put her on LDN. Neither of us know if we can get Naltrexone from doctors in Canada or where to buy it, but I've found places to contact and some are still going to get back to me...one day over the rainbow... I look forward to hear from you, and you could write Heidt that has other information that I don't have- Her email is Cjheidt@... and she would really look forward to hear from you and even meet up with you since she has relatives in Calgary. ps I think I am with the 's group. I think I'm getting bloggered by others for somereason or other, very MS for me if you ask me... ndoyle <ndoyle1@...> wrote: Hi , Like you, I’m on a mission to find out as much as I can about LDN and how I will overcome any obstacles on obtaining this drug in Alberta. I’m going to see my GP in the middle of April and I’m hopeful she will give me a prescription as of this moment I’m just beginning this quest and I will keep you and others informed as to how I make out. Can you tell me what is a blood print? I’m not understanding what has helped your symptoms, are you on LDN? If so, did you get it from your GP and can you buy it in Alberta? Nice to know I have someone in this corner of the world to relate to our same concerns. from Calgary From: low dose naltrexone [mailto:low dose naltrexone ] On Behalf Of LuikSent: Saturday, April 08, 2006 6:46 AMlow dose naltrexone ; helpforms@...Subject: Re: [low dose naltrexone] Hopeful new ms member Hey Calgary, I am from Edmonton and everyone here says LDN don't exist in Canada. My friend with MS as well has been looking high and low for information but I'm more into doing things like this, joining this group. I am 46 and got my diagnose in 1997. I use to have symptoms like you too, then last year, I went to a Doctor Sandhar in Edmonton, he did a Blood Print on me, and now all those symptoms are gone. I almost went on Copexone too, but after the MS Specialists and Neurologists were blown away by my improvement so Copaxone can wait. But I would like to get more Canadian Information on why both of us, that have some of the same doctors, try keep us from knowing or even testing LDN out. (And, if you want to know more , since you are around the corner from my City, to let me know. Okay? Let me know what happens. Please. ) helpforms <helpforms@...> wrote: Hi everyone,I have just found out about LDN and didn't realize there was a pill form that could maybe help my ms. I'm 44 yrs old and I was dx with rrms in 2001. I just discovered all the testimonials and got very hopeful and excited.I've made an appointment with my GP for a prescription and hope I have as much success as everyone I have read about. I also struggle with numb & tingling hands, both my legs feel like a new born colt trying to stand and have the bathroom habits of a 2 year old who has had to much juice to drink. I have to joke a little it helps to keep me going. I have also just started feeling the effects of fatique, wow, talk about dragging you down, no energy whatsoever. I use to walk 5km a day and lead a fairly active life, I feel so robbed and defeated so I'm hoping I will have good luck with LDN just a little quality of life returned to me would be great! My neur. also wanted me to start the CRAB drugs and I said I wasn't ready for that, I hate the thought of needles and all the side effects they could give me. I guess that is why LDN is so appealing because everyone is saying there are very little side effects. Looking forward to meeting new friends online and what LDN will do for me and hopefully I'll be able to help someone else. Bye for nowI'll keep you posted, from Calgary, Alberta Canada Make free worldwide PC-to-PC calls. Try the new Canada Messenger with Voice Make Canada your Homepage Canada Homepage Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 13, 2006 Report Share Posted April 13, 2006 To from Calgary Did you get my message??? Elizabaeth from Edmonton ndoyle <ndoyle1@...> wrote: Hi , Like you, I’m on a mission to find out as much as I can about LDN and how I will overcome any obstacles on obtaining this drug in Alberta. I’m going to see my GP in the middle of April and I’m hopeful she will give me a prescription as of this moment I’m just beginning this quest and I will keep you and others informed as to how I make out. Can you tell me what is a blood print? I’m not understanding what has helped your symptoms, are you on LDN? If so, did you get it from your GP and can you buy it in Alberta? Nice to know I have someone in this corner of the world to relate to our same concerns. from Calgary From: low dose naltrexone [mailto:low dose naltrexone ] On Behalf Of LuikSent: Saturday, April 08, 2006 6:46 AMlow dose naltrexone ; helpforms@...Subject: Re: [low dose naltrexone] Hopeful new ms member Hey Calgary, I am from Edmonton and everyone here says LDN don't exist in Canada. My friend with MS as well has been looking high and low for information but I'm more into doing things like this, joining this group. I am 46 and got my diagnose in 1997. I use to have symptoms like you too, then last year, I went to a Doctor Sandhar in Edmonton, he did a Blood Print on me, and now all those symptoms are gone. I almost went on Copexone too, but after the MS Specialists and Neurologists were blown away by my improvement so Copaxone can wait. But I would like to get more Canadian Information on why both of us, that have some of the same doctors, try keep us from knowing or even testing LDN out. (And, if you want to know more , since you are around the corner from my City, to let me know. Okay? Let me know what happens. Please. ) helpforms <helpforms@...> wrote: Hi everyone,I have just found out about LDN and didn't realize there was a pill form that could maybe help my ms. I'm 44 yrs old and I was dx with rrms in 2001. I just discovered all the testimonials and got very hopeful and excited.I've made an appointment with my GP for a prescription and hope I have as much success as everyone I have read about. I also struggle with numb & tingling hands, both my legs feel like a new born colt trying to stand and have the bathroom habits of a 2 year old who has had to much juice to drink. I have to joke a little it helps to keep me going. I have also just started feeling the effects of fatique, wow, talk about dragging you down, no energy whatsoever. I use to walk 5km a day and lead a fairly active life, I feel so robbed and defeated so I'm hoping I will have good luck with LDN just a little quality of life returned to me would be great! My neur. also wanted me to start the CRAB drugs and I said I wasn't ready for that, I hate the thought of needles and all the side effects they could give me. I guess that is why LDN is so appealing because everyone is saying there are very little side effects. Looking forward to meeting new friends online and what LDN will do for me and hopefully I'll be able to help someone else. Bye for nowI'll keep you posted, from Calgary, Alberta Canada Make free worldwide PC-to-PC calls. Try the new Canada Messenger with Voice Have a question? Canada Answers. Go to Canada Answers Quote Link to comment Share on other sites More sharing options...
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