TOPIC:

My name is Jason, I live in the US in the state of Michigan. I was born with the supposedly incurable disease:
en.wikipedia.org/wiki/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

Great testimonial Jason, thank you for sharing it!

And welcome to the forum!

That is interesting the baths were a breaking point for you. For me it was the bag treatments once I got up to 1/2 tsp doses and 20 minutes in the bag (genesis2forum.org/index.php?option=com_kunena&func=view&catid=28&id=3054&Itemid=66). For about an hour afterward my pain and fatigue would go away more powerfully than I had every experienced. I knew then it was pathogens and I need the bag treatments. I am still doing them every day.

I bet if you get enough MMS and other support for your body, it will heal itself. I have heard stories like that with many natural therapies. Please do keep us posted. I think you are doing a great job.

Michael

God Bless You enigma182! I love your spirit!

OK well that was my letter to join and I wrote that a few months ago. Here is where I am now:
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.

So far I get herx reactions from the 6 drops and I am thinking I will need to go down to 4 or 5 drops as I end up not taking more than 3 - 4 6 drop doses per day. The thing that is really driving me crazy is my sinuses still have not cleared up. I have tried the sinus rinse with 1 drop per oz of water into a sinus rinse bottle. The problem is this makes my nose swell completely shut and it burns pretty badly. Is that normal? If not what should I do? I am trying to keep the baths to every couple of days so I have the energy to take care of my newborn and toddler, they require lots of energy and attention. I was really hoping to see better results by now. I am welcome to suggestions, I have not tried a bag treatment yet as I dont have the time with also watching my children.

I suspected candida earlier on as I had some issues on the out side of my lower body which I have now mostly cleared up with the baths and the body spray. Maybe I need to have a special diet to kill the candida? I was so excited when I got some energy back after I initially tried the baths but that was a few months ago and I am not feeling energetic anymore. Anyways I am so ready to turn this into a positive experience.

As a side note I have been making my own mms per the instructions in the book. I purchased bulk NaClO2 and citric acid powder from the internet. My MMS mixture turns a nice dark yellow and smells very much like chlorine when mixed ever though my nose is not fully clear. Also I can usually move air thru my nose but not smell thru it isn't that odd?

Also i have been mixing my MMS with a juice from the store available here in michigan. It is called simply lemonade. I noticed there is a small about of pulp still in the juice and I read the info in the book again about not having pulp in it. This is the only juice I can find that doesnt have added vit C. Has anyone else used this and if so is it ok? I imagine I would not be getting the herx if it didnt work but I am trying to rule out anything that woudl effect killin off this stupid sinus infection. I have has sinus congestion for as long as I can remember so I am eager to be healthy.

Also I had a lump in my right breast that I have had since my teenage years. The doctor said it was normal and alot of males get them under or close to the nipple and it is from hormones. In women it would grow into adult breasts. Anyways all that being said it is now gone

My lungs are clearer, however I am coughing mucus up, I also hope to clear them up however I am worried about the breathing treatments as I have had asthma since my teens.

Well that is the road so far, I am sure I forgot some things along the way and I seem to have rambled on alot. Thank you for the encouraging words.

That nasal rinse 4 drop per 4 OZ made my nose swell shut too.
4 drops per 8 oz of water worked much better. It still tough to take but my nose does not swell shut now.
I use my neti pot with the saline solution much nicer on the nasal tissues.
You can find neti pots in some heath food store and on line pretty reasonable price. You can make your own if your so incline. I use sea salt instead of the Neti pot brand of salt.

Well another month goes by and still no cure but I am not feeling worse as long as I take at least a 6 drop maintenance dose each day. I am beginning to suspect that my candida is now fighting back against the MMS and has been for some time. I really need to get this under control. I have read about changing my diet and some other things however going all raw foods and non GMO etc is pretty expensive also I don't see any suggested diets does anyone have a link maybe?

I took only mms2 at 4 caps per day for about 12 days and stopped that about a week ago then resumed my maintenance doses of mms1. I was really hoping to not be ill after so many months of going on and off protocol 1000 and 2000 as well as taking at least 1 or 2 mms baths a week. however my nasal passages persist in being clogged with mucus and the ringing in my ears is still there as well as general fatigue and, a stupid persistant eye infection. The fatigue is lessened since I stated the mms and my depression is more under control and I can usually kill off a cold or bug withing 4 hours if I take a dose of mms with the onset of symptoms. So I am benefiting from the use of it just not feeling energetic and healthy.

I was trying to do the 4 drops in 8oz of water for a nasal rinse however that still burns like crazy is that normal? Also my nose is usually swollen shut about 90% for about 30 - 60 minutes afterward. Would bentonite clay be a better option? Should I rinse with it, and what about drinking a certain amount per day mixed with water. I really am looking for help here. Anyways thank you for reading, I hope you all find happiness and health. Take care and have a nice day.

enigma, most nasal washes are actually a mild saline solution - personally, I'd start with the saline solution and add 1 activated drop of MMS. Once that's good, then I'd go to 2 activated drops, added to the saline solution. I think you need to buffer it a bit. NOW, I'm "guessing" here - have not done this - but this "makes sense" to me.

Thanks pam, ken, and tish.

I am still plugging away at this, I am currently only taking a 6 - 8 drop maintenance dose per day and doing the saline nasal rinse with 2 drops of activated mms. This doesn't burn or burns very little however I am not really kicking my infection. I do have mercury fillings and I will most likely have to get them removed. Unfortunately this is an expensive process and I think the ADA should have to pay for it since the damn amalgam is so poisonous and they still say its . k. Anyways, if I can ever get that done maybe then I will regain some more of my health. Unfortunately I will probably lose most of my molar teeth as they have basically fallen apart which sucks seeing as I am only 31. I think most of the issues with my teeth are due to all the medication I have been on.

So far the MMS does seem to be helping and will usually kill a cold/bug within a day or two if I am vigilant about taking it. That may seem like a long time however I would like to point out that my IGG is only existant via an IV injection per month which is very costly and, my IGM and IGA are only approximately 10% of normal and cannot be boosted via injections or IV's. These are what fight off infections before they get a foothold etc. I normally would have to endure a week or two of antibiotics to kill off the sickness that MMS usually kills off in only a couple hours. My biggest worry is that I am not gaining in energy. Once I go thru a round of protocol 1000 should I wait a certain amount of time before doing it again?