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Showing Visitor Messages 1 to 10 of 14
  1. Will
    07-11-2013 10:31 PM - permalink

    If you send me an email, I can send out Jim's Regimen.

    Best Wishes

  2. Caliburn
    07-11-2013 05:49 PM - permalink
    I took two scoops of noxplode every day for a year, from the october before this october to this past november when my symptoms started. Sometimes i would take it when i was having beer after the gym. Did you take this stuff also?
  3. cypress
    06-14-2013 06:54 PM - permalink
    Nothing new on tb4 , I am actually cutting back for a while after adding baicalin and dexamethasone Want to see what those do

  4. kiara
    05-26-2013 04:44 PM - permalink
    Hi, my vision isn't normal yet, I have this double vision going on almost every day but not all the day, it comes and in your case I also have wasting in hands feet thumbs calves and the specialists are concerned about this because is not a symptom of neuromyotonia. They said there is also a disease called myotonic distrophy that can cause muscles wasting and myotonia but first thay want to rule out autoimmune problems. They said sometimes even autoimmune problems can cause atypical symptoms like muscles wasting and vision problems. I also have some strange symptoms like difficulty swallowing, problems chewing, feeling as if sometimes my jaw is locked and it's hard to open my mouth and also neck pain and's really a mess. I'm glad to know you have a better mood and good sleep....anxiety doesn't help and makes our life even harder. Keep me posted about you, talk soon Kiara
  5. kiara
    05-25-2013 12:41 PM - permalink
    Hi Derec I had the tests yesterday. I haven't the results yet but during the emg they said they found fibrillations, fasciculations and myotonic discharges in almost all the tested muscles, they said it doesn't seem so bad cause despite these findings my motor units appeared to be normal in numbers and amplitude. They explained me that motor units in als are decreased in number and large in amplitude so in my case it doesn't seem to be als. I had a blood test for antibodies against potassium channels cause they think I could have autoimmune neuromyotonia....we'll see. I also had evoked motor potentials that were normal and a single fiber emg that appeared normal too. Now I have to wait for the results and then I will meet with the specialist again. What about you?
  6. cypress
    05-17-2013 10:36 AM - permalink
    cypress usually cheapest source, southern research higher priced option
  7. cypress
    05-17-2013 10:34 AM - permalink
    Yes I still take tb4 injections 2mg/ weekly. The propofol is amazing though.if you have als, find an excuse to undergo general anesthesia with propofol.
  8. here4her
    05-15-2013 11:03 AM - permalink
    Hi derec,

    O.K., good. You should be able to download and print out the protocol from that site. I also wanted to give you the name and number of the guy who runs that company (nutrivine).

    He (and his dad); Mike Siers 1-(561) 309-0948

    Paul's email address is:

    He is very helpful and has been 'doing' the protocol for a while now. My wife is just getting started....she has to psych herself up for it.....lotta 'stuff' to add to your routine.

    Hope you get it soon and get started asap. Please keep us informed.

    Hang tough,
  9. kiara
    05-14-2013 01:05 PM - permalink
    Hi Derec, I read your message to tb12 saying you have problems with your joints popping and cracking. I have the same problem, I developed the popping and cracking of joints when all this mess started and it's getting worse and worse: all my joints cracks hard when I move and it's not normal. Let me know how you're doing, wish you the best, don't lose hope you're so young. kiara
  10. here4her
    05-14-2013 11:23 AM - permalink
    Hello derec,

    I think the person with the most experience on this forum with the DP is dbltree.

    However, we signed up for the DP for my wife, received it within 3 days of payment. We only took the first 7 items on the list that are highlighted as 'most important'. The AAKG, are AKG the main work horses, and the other 5 work in conjunction with them. Of course, you could do the entire protocol, if you have the money and access to all the meds.

    I am not 100% sure that they ship to Europe, but I can't imagine that they don't. It would cost a bit more, naturally, but should be well worth it. We paid $316.45 US for a one month supply, shipping was free (this time). The company that has these supplements is called Nutrivine and is located in Florida.

    I have the contact information, and can tell you more, if you are interested. Send me a visitor message, and I will give you dbltree's email address, #'s that you can call for info.

    Hang tough,

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  • About derec
    What's your relationship with ALS/MND?
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  • Last Activity: 12-09-2013 09:34 AM
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