Ah ,I've always admired your spirit of inquiry and courage to experiment. It has definitely inspired me!I think I'll do the MSM/CS pierced capsule under the tongue (45 min) daily for a couple weeks, and then stop and try MSM in my morning CE. It will

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Ah ,I've always admired your spirit of inquiry and courage to experiment. It has definitely inspired me!I think I'll do the MSM/CS pierced capsule under the tongue (45 min) daily for a couple weeks, and then stop and try MSM in my morning CE. It will be interesting to see the difference.I like the idea of adding Nato, Lumbro, and Sera with the MSM. Must try this after an initial trails of MSM or i'll never know what did what. Will keep everyone posted.Having a CE discipline already in place for so long, it's a wonderful 'port' for trying other things thte gut may not like or may destroy. Again, you were one of the inpsiring people to get me to try CEs. What a difference they have made in helping the detox side of this Lyme fight!Be well, my friend,Léna Hi Lena, While in Mexico, my doctor was doing IV therapies on my husband who has cholesterol and arhythmia problems. He put a lot of DMSO in the IV. He used so much that our entire house smelled like DMSO for a day. MSM is a derivative of DMSO without the solvent and is a good source of Sulphur. MSM is suppose to mitigate the negative side effects of the DMSO such as the smell and skin irritation. DMSO is only legal in this country by prescription whereas MSM is considered a supplement. Since they both are good for resolving inflammation as well as driving other medications into the cells, I would think that MSM would work well in a CE. Since the solvent part of the DMSO is removed when producing MSM, I would think it would be safe to the delicate mucousal lining. Whenever I put anything in my CE, I always do energetic testing to see if it will be in the highest and best interest of my body. You know me, if I think something has potential to be helpful, I go for it. For the past 10 years I have been my own experiment and after my MD started giving my Glutathione IVs and learning that it cannot be absorbed through the digestive tract, I decided to try the liquid Redisorb Glutathione in my CE, to see if it would be beneficial that way. Years later, someone came out with a Glutathione suppository, confirming that it indeed would work this way. I have opened EDTA capsules into CEs and I personally feel that it is almost as good as taking the stuff IV. Since it is expensive to do IVs, I find that the CE is a great delivery method for many things. I put drops of trace minerals in my CEs. I have opened probiotic capsules into CEs and had considered putting Natokinase, Lumbrokinase or Serapeptase capsules in the CE to target biofilms in the blood. I wonder if putting MSM together with Serapeptase would actually drive it into the biofilm better. Hmmm... something else for me to try! Give MSM a try and see how you feel, you might find that you will need to back down on the dosage since it goes right into the blood. I would start with half the capsule and if it doesn't address the inflammation bump it up a bit. Let me know how you do, I may give it a try as a means to drive things deeper into the cells. Thanks for the idea!! > > > > > > > > > > > > Hi all, I want to report what is going on. I started at 1/4 > dose enema a day and worked up to 1/2 dose and I am now doing 1 drop- > dose a day(enema). I have a sense of clarity in my head/brain that I > have not had since this became full-blown 1.5 years ago. Their are > actually times my brain almost feels at 100 percent. The other times > 75-85 percent. My head was bad! I am also feeling stronger, a bit more > strength and energy and I am fooling and joking and being silly with > my 6 year old again. I am not saying I'm cured....but have taken a > nice leap in the right direction. My son said: Mom, I feel so happy > when you are feeling better > > > > > > > > > > > > I know some don't agree with what I am doing and that is > fine. BUT I am a determined mom that has gone broke fighting for the > life of her son since he was very young, diagnosed with autism and > pretty much failure to thrive. I don't have the luxury of a rife or > coil but do have the MMS! I was dearly afraid of my life....but I am > fighting back with the MMS and I am determined to do what it takes. I > have a six year old that needs his mom-well! > > > > > > > > > > > > So I will continue to report what the enemas are doing for > me................maybe it will help others to make their own > decisions as to whether it may work for them or not. Paying it > forward .............for whatever it is worth. Jodie L. > > > > > > > > > > > > > > > > > > > > >