MMS use associated with improved energy and nasal breathing in X-linked aga
My name is Jason, I live in the US in the state of Michigan. I was born with the supposedly incurable disease: X-linked_agammaglobulinemia
I am entrapped into a system of health care and cannot seem to free myself, I have scoured the internet in search of a cure for my condition or at least a means to survive once Obama Care comes into play. My first success with MMS was with an abscessed tooth where the infection had spread down my neck and into my ear. It was extremely painful, and thanks to the wonderful governor Granholm of Michigan who cut out dental care from the medicaid program I had no dental coverage. The MMS worked within a few days I was mainly without pain but the herxheimers were bad. I quit taking MMS at that time because my doctor wanted me to take a large dose of antibiotics before he pulled the tooth, which I had to do if I wanted it out. Since the tooth was a wisdom tooth and more than 2/3 rotted/broken out I complied. After this I felt relatively healthy except for catching roto-virus twice (which I realize now was do to my stopping the MMS). I felt better after the tooth was pulled and I thought the MMS might have made me ill.
My second success so far came for me after much study of MMS & chlorine dioxide; when I tried to convince my mom that it would cure her diabetes which is steadily getting worse. She refused to take the MMS because its not FDA approved… So to show her that it works I will do everything I can to cure myself of this dreaded illness. So far I have been following protocol 1000 as close as I can and taking 20-25 drop MMS baths twice a day, in addition to putting MMS drops in my eyes ears and nose. The baths were absolutely the breaking point. I awoke the next morning with 2x more energy than the previous day. I am fairly certain I am awash in virii,bacteria,yeast etc you name it. I have been on so many antibiotics and I get infusions of gamma globulin each month. I am keeping track of my counts and so far they have slowly gone up. I will continue to track this information and I will let you know asap if somehow I am cured. I have added a couple 1/4 capsule pills of mms2 during the day but so far it really upsets my stomach.
Due to my own diligence in trying to find real answers about my condition I found the average lifespan of a PID patient was 42 years. I want to thank Mr Humble from the bottom of my heart. I struggle to find the words that properly convey my appreciation for his selfless acts. For the first time in 15 years I can breath through my nose for at least 90% of the day. I have more energy than I ever remember having and I can breath deeply into my lungs without feeling like someone is sitting on my chest. I pray for all of you every night and will continue to do so until we are free or we are dead. Thank you Mr. Humble for giving me hope for the future and the possibility of seeing my children grow old.
I purchased your book and wish I had the funds to help more, however I am on a fixed budget of less than 800 a month so things are very tight I will help somehow even if its only by spreading the word and sharing your book. I encourage everyone to buy it and I will continue to discreetly help as much as I can.
Take care and God Bless You All
Jason
{2/29/12}
…I worked my way up to protocol 1000 for about 5 weeks along with a full size 0 mms2 capsule 2 – 4 times a day. Also a 20 – 30 drop bath usually at least once a day sometimes only every other day. Then at the end of January I took a break for about a month to let my system clean itself out and I wanted to see if my nose would stay clear.
My nose did not fully clear up and I am also still very tired. So 3 days ago I started back on the MMS but I have gone to 6 drops an hour of just mms1. So far no diarrhea but I am a little tired. I will add more to this but I have to go for now.