Can Chlorine Dioxide cure Pneumocystis jiroveci pneumonia PCP?

Hi,

My father was just diagnosed with Pneumocystis jiroveci pneumonia (PCP), he is 78 years old. The doctors say it may be due to the R-CHOP chemo he is on. My question is does anyone know if PCP is an anaerobic bacteria that could be cured with MMS/DMSO? If yes which protocol is recommended?

Thank you very much for the urgent response!

A google search tells me this is fungus based issue.
MMS eliminates most fungus. The one/few that do not respond to MMS are dealt with using Aztec Clay. See Aztec clay thread in recent discussion.


keep in mind that diagnosis is not always correct.
PC1000 or Aztec clay are the protocols that come to mind.

Thank you Rev Ray, I will check it out! What bothers me is that he has been on PC1000, without DMSO, for a week and a half and he stopped it a few days ago, then yesterday we took him to the Dr because he was not feeling well. The Pulmonologist looked at the CT and thought it was PCP, he said he needs to do a biopsy Monday to tell for sure.

He started the 1000 protocol again last night and is feeling a little better, I am now testing him for DMSO allergy and if no symptoms I planed on adding it but was not sure if it was the right thing to do.

I also started him on the Budwig protocol last night. He lost too much weight and could not eat much.

I'm not sure Bud and MMS are compatible.
MMS is OXIDATIVE and Bud w/o looking may be anti ox therapy which conflicts and prevents either from working in some cases.

Given that MMS does seem to help improve condition, I think we can say MMS is helping.

MMS wrks very fast in the lungs IF there is nothing of concern between blood/MMS and lungs.
Also see www.mmswiki.is and see the breathing protocol. This may help faster.
Doc "thought" it was PCP....
Wouldn't it be great to more less resolve this before any painful biopsy invasion?
Remember MMS is far superior to any western meds of any kind, period.
So if he is improving on MMS, that is the best course of action in my opinion.

Ron I also want to let you know fungus is a cause of Cancer and not the other way around.
g2cforum.org/index.php/list/testimonials-of-experiences-with-mms/27873-fungus-digestion-sinuses#41631

Yes I understand about the microbes are the cause of the cancer, we discovered MMS a little too late...

I gave him two of the breathing protocols, Tuesday night and Wednesday morning. Not sure if it helped or not, Wednesday morning he seemed to be fine but then yesterday morning he was in bad shape.

Very confusing and that is why I decided to post here and ask!

Not sure about the Budwig interfering with the MMS, but out of desperation seeing him loose so much weight and not wanting to eat, I decided to give him the Cottage cheese and flax seed oil, to help his cells regain the 70mV they require to operate properly. Again, I am not sure if the MMS and Budwig interfere with each other, I tend to think it should not but I am not sure!

A quick review indicates Budwiggers also believe antioxidants is not the best approach.
There is talk of Omega 3 and 6 needed. That fish oil may be better than flax oil.
Rancid oils, from freezing bread to other means of fouling cause the oils to become rancid. When this occurs the cells that use fat around them are now unable to intake insulin and is thought to be cause of diabetes and cancer and other conditions due to cells being blocked by rancid fat.
I read that the rancid fat is replaced by new oils ingested that are good/clean.That is what you are doing with Bud I think, replacing bad oils with good.
Sat increases cell conductivity, sugar depletes cell conductivity.
MMS is a salt, with a voltage of .95V that may also activate or recharge cells.
Many feel a surge of energy or well being when using MMS initially.
He needs to eat something for sure.
He is in good hands.

I wanted to post an update on my dads condition. He was taking MMS protocol 1000 for 2.5 days straight and then when by day 3 when his condition did not show any sign of improvement, he decided to stop. He felt very dizzy and weak, could not eat and barely drink, had to force himself.

I was really hopping that by now his lungs would clear but it did not look like he was getting better at all. This morning I took him to the hospital and they gave him broad spectrum antibiotics. I am not sure if it had to do with that but he is now feeling a little better, he even felt hungry , which was the first in two weeks.

At this point I am a little disappointed and confused, I would have expected the MMS to take care of the lung infection, which the Dr think it is. Today they did a CT and tomorrow we will get the results. I will try to post an update tomorrow.

3 days is not long enough - unfortunately - guessing that his belief in antibiotics is probably helping him

2.5 days is not long enough for this type of condition.
How many drops were consumed in 60 hours?
MMS is FAR more powerful than any antibiotic.
It sounds like the MMS was used up elsewhere in body or deactivated with caffeine or some anti oxidant and not reaching lungs.
There is a reason he is ill, and toxicity is an issue.
So when MMS enters stomach and blood stream it counters the first issues first.
Know that antibiotics will kill good stomach flora and leave you w/o an immune system. That whatever is treated with AB will likely return. And be resistant.
There are 29 reasons people do not heal using MMS.
Here they are, 29 Reasons

Thank you! But he has been on MMS for a week and a half prior, and he got the infection, that is what I don't understand, believe me, I was really frustrated and confused. Maybe the CD was interacting with the chemo and 3 drops was not enough? I was just ready to introduce the DMSO...

I to believed that MMS is much stronger than antibiotics, I am VERY much against them. It destroys the gut flora. I showed my dad how to make kefir and yogurts, we use raw grass fed cows milk and goats milk. So believe me I did not want him to go on that. He was suppose to go to the hospital Friday, but I waited all weekend hoping the MMS would work.

I was on the 3 week 1000 protocol, my brother is also on it, he has Lyme, it definitely helped him.

I should add that his O2 level was very low, they had to give him O2 so maybe that is why he is feeling a little better, not sure.