Aspergillus and MMS

Has anyone here ever got rid of aspergillus by breathing in MMS?

Also, I've been searching the web over and over and can't find a real break down on exactly how to breath the MMS... I know you don't use more that 3 drops at a time, don't drink it straight, breath lightly...all the average info that one can find...

I need to know how many times a day, like a schedule or something....anyone care to shed some light?

What one must consider when using chlorine dioxide or mms is that it needs to come in contact with what your trying to kill. No contact, no kill. Contact time is also important. Breathing in chlorine dioxide for a few breathes is probably not as good as breathing it in, all night, in a lower concentration. You could try making a solution of mms and activator, place it in your bedroom while you sleep. Have it far enough away so you can't smell it but close enough that you'll get some chlorine dioxide while you sleep. Because the chlorine dioxide is a gas trapped in a liquid it will release slowly through the night. A bowl will release it faster than a glass. What you would need to determine is, how mms to activate. I'd suggest start slowly and build up over a few nights. Hope you find this helpful and if you could keep us posted as to the effectiveness of this. Thanks

Thanks NZDUTCHIE. The reason I'm asking is because my father has been given two weeks to live. He has AML which is coming back strong, but the doctors are more worried about the fungus pneumonia taking him out more than the AML at this point.

Please give me your guys advise on this.

I am activation 2 drops and having him lightly breath it in at 1 breath of MMS to 5 breathes of fresh air. He's doing this for 15 minutes every hour, and kind of at random. I'm thinking about doing it every hour 8 times a day. Does this sound OK? Should I be more or less aggressive?

Also, he is neutropenic....

I think in your father's circumstance, aggressive is the way to go. Have you seen any progress so far? Is he ingesting activated mms as well? . There was some info about dilute hydrochloric acid being able to boost the body's white blood cell activity.
www.keelynet.com/biology/hcl.htm

Our prayers are with you.

I've had him breathing the MMS1 for about 3 days now and I want to say that he is talking a little better but I really won't know until they do more chest X-rays to look for the fungus pneumonia nodules. If they show that they are shrinking then we will know for sure that its working, right now its unknown.

All he does is sleep 24/7, while he's sleeping I hold a cup of mms next to his mouth. Not too excessively though...

Question for everyone here... What works better on Aspergillus, MMS or Colloidal Silver?

And no he his not drinking the MMS just yet. I just started him on the CS, I also just read the MMS is canceled out by CS...trying to figure out what would be the best option for him. Thanks!

Also, I just want to point out to everyone that PAM has posted on almost everyone's post on the forum but for some reason has decide not to partake in my discussions.

I guess when your too blunt and direct she decides not to help.

MikeAML wrote: Also, I just want to point out to everyone that PAM has posted on almost everyone's post on the forum but for some reason has decide not to partake in my discussions.

I guess when your too blunt and direct she decides not to help.

Shame on you. Pam is a busy lady and a kind person. Those of us on this forum are very fond of her. You are surely out of line. Please stop.

I have no experience with CS so would have suggested MMS internally. Have a look at this www.facebook.com/photo.php?v=10150991514880160