Naltrexone used for ms

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Naltrexone used for ms

Posted Apr 21, 2016 by Admin

I climbed mountains and breathed the thin, clean air with a renewed joy of life that I feared would never be a part of me again. My husband is pleased to have his wife of 42 years back by his side and my Mother cried.If anybody whispered that something had an anti-tumor property, I was right there looking into it. Over the months and years, I have gone through it all. I first had radiation to shrink the tumor enough to think and breathe. Nobody was interested in helping, as there was no money available. Then in January 2012, Obamacare kicked in and I was able to get pre-existing condition insurance for 426 per month.

There is also lots of free info at http www. LDNers.org, http lowdosenaltrexone. org, http LDNN ow. org, http LDNS cience. org and many other websites with tons of information and references.Unfortunately, the cancer jumped to the psoas muscle of my left leg. That is the muscle that starts at the spine, goes through the pelvis and attaches to the front of the femur, to lift the leg.

The mental fog is rapidly lifting, and I can now remember a phone numbers, which had gotten difficult. It has not made a big difference in the heat problems, but I will learn to live with that.Customers who bought this product also bought.

I was diagnosed with MS in September 2000, when Texas had nearly a week of 100 temperatures. I had no idea that it was partly the heat that was so debilitating, but it finally landed me in the hospital, where I spent an extra day.Now at 61, after being on LDN for only a couple of months, I have just returned from a trip to the Colorado Rockies where we took two of our horses and rode for 1-2 hours a day, for over a week.

Best of all, the heat intollerance has gone, as well. I am not sure exactly when it started to fade, since it was probably in the autumn when the weather was getting cooler anyway.What it has helped with is no more fatigue, I sleep like a baby through the night, my cognitive function is vastly improved, my left leg and right arm are no longer nearly useless, but as normal as they were as a youth.

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I read the newsgroups and find myself drawn into the lives being helped by the LDN just like mine. Someday, I hope to be one of those who is announcing her fifth, tenth or twentieth anniversary on LDN.Well, it is almost three years since starting LDN and to date, NONE of my symptoms of MS have returned. Sure, I probably still have MS, but if I don't have to suffer from the symptoms, then it is kind of a moot point, right.

I am still somewhat atrophied from years of not being able to use my body the way that I wanted, but the muscles are coming back almost as quickly as the memory.I hope to stay in remission, just like I have been free from MS, for so many years).

I know you guys are here for the story of MS, so I will start with the fact that after 5 1/2 years, I still have no symptoms of MS. I went from nearly bed bound, to essentially normal, with the use of LDN.It alone cannot solve every problem that comes with our less-than-healthy lifestyles. But it can give us a good start and also give us the tools to start on the road back to health.

No more of the uncontrolled fatigue that would overcome my life. The mental fog lifted too. I'm not sure if I have a photographic memory like old times, but I can remember a phone number that I have dialed once, and that had been gone.Today is my one year anniversary on LDN. At this point, nearly all of my MS symptoms have been reversed. First to go was the fatigue. Sure, I'm over 60 and still get tired, but it is an honest tired from actually getting things done.

I find them self serving, money focused people with no quest for information. I have not found one interested enough in what I have done to "cure" my MS, or now, to totally cure my cancer, to even inquire.I realize that the ABCR drugs help support the MSS, but the Society is there to serve us, the MS patients even if it means that the thousands that we all spend on expensive and scary drugs is cut way down by the use of.

Looking back, I know that a part of my recovery came from finally having the energy to take better care of myself. We started eating better, taking good supplements, and generally living a healthier life style.Then went for chemo, but I did not count on the doctors to have the answers. My history with doctors is a real love/hate relationship, with an emphasis on the negative.

Even the 900 per month insurance payments would put us in the poor house. I had no alternative but to do the research on my own and see if there were something else out there that would make a difference in my life.Update December 14, 2014 Last May was 5 years on LDN, and a few days ago was 3 years since being turned over to hospice to die. A lot has happened in that time.

I am so GREATFUL that I found LDN, the new protocol for using Low Dose Naltrexone to help repair the immune system and put my symptoms in remission. I cannot adequately express the difference that LDN has made in my life.I cannot thank my lucky stars enough that I lost my health insurance and found Low Dose Naltrexone. If anybody else wants to try it, there is a Yahoo newsgroup with 10,000 happy members who are willing to tell their stories too, and help in.