Announcement

Collapse
No announcement yet.

I think I found some HOPE!!

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

    I think I found some HOPE!!

    Quite a while ago I posted on one of the forums asking if anyone has ever heard of RBTI. That was when I was still researching it and was hoping to find others with MS that have tried it. I was unable to find anyone but I did find a lot of other positive results when using this way so I decided to just go ahead and give it a try. I did not want to share anything until there was something to share, whether good or bad, so others with MS would know.

    The basics of it are that your body must be remineralized in order to begin healing. RBTI uses your own body chemistry to help decide what foods, vitamins and minerals are and are not good for you at this moment. You test yourself (a series of tests you perform on your urine and saliva - it only takes about 15 minutes) every two weeks and call the numbers in to a professional who knows how to read the results and knows what to suggest next. As the body begins to heal and repair itself, your adviser will suggest what vitamins and minerals to take or not take and be sure you are on the right track with your food still.

    The one who reads your numbers does not want to know ANYTHING about what you are going through. The ONLY thing they want to know is: your age, height, weight, male or female, and then your numbers. I was quite shocked the first time I called in and gave my numbers. Challen, the man who is helping me along, said all sorts of things that were wrong with me and it was amazing how he could tell all of that just by reading my numbers. But really, it's not a trick or anything ... he just knows what the numbers mean. (The numbers are your urine and saliva pH, your urine brix/carb/sugar number, your salt/conductivity number, albumin number and your nitrate nitrogen and ammonia nitrogen numbers ... sounds pretty scientific and I guess it is but it's easy to perform the tests at home by yourself.)

    Honestly, I have not felt this good ever since I started having MS struggles about 2 1/2 years ago. Maybe it is a coincidence?? I don't know. I started a blog to keep track of what is going on and to share with others who are interested. I have the blog linked in my personal profile if anyone is interested in looking at it. Also, feel free to ask more questions if you are interested. Like i said, maybe it's all a coincidence and I am just having a really, really, really good 'relapse'? But I have been really slammed with MS this past year and it just seems impossible to be coincidence ... but maybe it is. Time will tell. In the mean time though, I am very happy to keep doing what I am doing and seeing what will happen.

    Joanne

    Not officially diagnosed due to non-MS-specific spots on MRIs, but the neurologists all agree it's MS.
    Frustrated. January 2019: finally saw an MS specialist worth seeing. Maybe we'll get to the bottom of this.
    EDSS of 5.5, sometimes 6.0

    #2
    I'm glad you feel better.

    I took a quick look through your first entry and I am curious... did you eat a lot of processed foods before? Any switch to more whole foods and less processed will always make someone feel better.

    I have to say that I was taken aback by his suggestion to stop taking all supplements and that he was against vitamin D especially since there is more and more research coming out about the benefits of high vitamin D especially for MS patients!

    Comment


      #3
      interesting ideas

      This kind of concept can also be done with a herbalist. They too can help you find your chemical balance.

      As always, caution and research is good on things that we use or take with any condition. Make sure that the person that you are working with has good credentials and, maybe even board certified, and the products have been tested.

      I did not read the blog, reading things that have any kind of length does not go well with my MS brain.

      What works for some does not work for others.

      Thank you for sharing your information. I will work slowly at your blog. I like to see what others are doing and compare to what I have or seen others do.
      God Bless and have a good day, Mary

      Comment


        #4
        Originally posted by misslux View Post
        I'm glad you feel better.

        I took a quick look through your first entry and I am curious... did you eat a lot of processed foods before? Any switch to more whole foods and less processed will always make someone feel better.

        I have to say that I was taken aback by his suggestion to stop taking all supplements and that he was against vitamin D especially since there is more and more research coming out about the benefits of high vitamin D especially for MS patients!
        For about 10 years or so I've been all homemade, from scratch, whole foods, lots of fruits and veggies, etc. I really love to cook.
        But before that I was NOT eating healthy. I was literally raised on fast food and did not do much better when I moved out.

        I understand your surprise about the vitamin D. I was surprised too but honestly, I am so desperate that I decided WHY NOT?! I might as well give this an honest go and see what happens. So far so good ... but I am not 'holding my breath' you know what I mean? I am encouraged though.

        Not officially diagnosed due to non-MS-specific spots on MRIs, but the neurologists all agree it's MS.
        Frustrated. January 2019: finally saw an MS specialist worth seeing. Maybe we'll get to the bottom of this.
        EDSS of 5.5, sometimes 6.0

        Comment


          #5
          update

          Just thought I'd give an update - I am currently experiencing another flare. It started pretty mild about a month ago but is worse here the last few days. Still not as bad as I know it can be. I am still hopeful and have seen other positive changes, but I'm realistic too.

          I plan to update my blog today if I have time.

          Not officially diagnosed due to non-MS-specific spots on MRIs, but the neurologists all agree it's MS.
          Frustrated. January 2019: finally saw an MS specialist worth seeing. Maybe we'll get to the bottom of this.
          EDSS of 5.5, sometimes 6.0

          Comment

          Working...
          X