{Part of original post}

I am a seriously ill person who has been diagnosed with both ALS and Lyme Disease…

I thought I had better qualify my previous statement. I now realize it sounds like I have both diseases whereas it is actually more of an either/or situation:

I am not sure if I have ALS or Lyme disease. I was diagnosed with ALS by a neurologist last May but 2 months later, I took antibiotics for an unrelated ailment (swollen glands) and I had a “Herxheimer reaction” (which should not happen to an ALS patient). Since August, I have been also given a working diagnosis of Lyme by an infectious diseases doctor (it can sometimes imitate ALS) and have recently had a weak/borderline positive Lyme test result from IgeneX labs in CA. So, my feeling is that I do have Lyme (with severe neurological manifestation of symptoms) and not ALS, even though I have been diagnosed with both.

{2/8/08}

I have been taking MMS for 1 month now. Currently, I am at 10 drops twice a day. I have had to stop and re-start twice due to extreme “herx” reactions. My goal is to get up to 15 drops 2x a day WITHOUT nausea. I got up to 15 drops before and had a violent reaction (the usual- vomiting and diarrhea) BUT I felt great for several days after the reaction subsided. I DO feel like it is getting to something toxic in my system and killing it.

I am still weak, have trouble walking and my hands are crippled from nerve damage. I do notice that some of my other symptoms are better or gone.

Better: fasciculations (twitching muscles), fatigue

Gone: tingling, facial numbness, blurred vision

I have been using MMS for MS symptoms just over 2 months and am seeing things which I love. For now what about the reduction of the skin lymph glands? I think this is a major sign of what may be happening inside all the other organs and glands. I had enlarged lymph below my breasts, under my arms and stomach. My holistic dr said they were swollen lymph glands. The computer allergist specialist said they had strep, mold and other virus and bacterial overloads. These glands are a part of the skin and look like fat deposits. I have had lymph massage drainage and this helped but nothing permanent. They the Lymph deposits on my trunk underarms, and lower stomach look like they are disolving. I also have small tumors around these lymph glands and they are too getting smaller. Does anyone know of anyone else with this experience. I think if it is doing this to my outsides it is also doing this to my pancreas, bowels (are loaded with glands, immune glands,)Brain in MS, and thyroid one side was swollen last week when I saw the dentist. I am also regaining better function with my Lungs. I would appreciate any support on this issue. Links experiences ect. Thank You