Urgent ! Need help with my dad with MDS related Acute Myeloid Leukemia

Mike, you are asking for advice from someone who has direct experience with this - it's possible that there's no one on the forum at this time who has that experience.

I can only speak from my training. Which I'm happy to share -

Jemco, I wondered what had happened to your brother-in-law - I remember your earlier post where they originally decided not to do MMS because it was inconvenient to their lifestyle. Thanks for letting us know.

Yes, that was my sister who said it was not convenient.
She's a nurse and was trying to do all the things that she was told by the "doctors".
He had been in remission after four or five courses of chemo and then when he went for another frequent test, they told him that it returned and he had two months to live and chemo was no longer an option.
That is when I suggested again the MMS and gave him the CDS.
Initially, he said he had a brief time while on the CDS where he told me he felt playful.
I am not sure if this was a placebo or if the CDS was responsible, but I am sure the CDS helped.
Towards the end, he was telling us he was very weak and then he contracted C-Diff and they said he had a bad sore in his colon, so they gave him antibiotics.
I remember asking my sister via email "Why aren't they at least giving him an antibiotic cocktail enema?". I don't think they acted on that.
If I were more in control, I would have certainly suggested an MMS or CDS enema.
Once they reported detecting the C-Diff, he only lasted a few days.
I think the lack of immune system resulted in no defense to the C-Diff.
I also think the chemo got rid of the immune system.
This was extremely difficult on all of us.
I want to say to my sister, "What is your strategy to fight something like this if/when it happens again?"
I haven't thought it was the right time to say it because partly, I don't want to make stress and partly I worry that her opinion of MMS hasn't changed and again, I don't want to cause her stress.

Jemco, I totally agree with you, and also agree that for those who don't want to know anything other than traditional treatment, there's not much we can do but love them and allow them to experience whatever it is they're going to experience. Hugz.

Mike:

Get your father on the MMS right away at home. Right now his immune system is way compromised by all the antibiotics and the poison from the chemo. Go slowly to protocol 2,000 if you can. You can get the info about the different protocols from this website.

Blood of patients with advanced cancer is populated by innumerable pathogens, many of which won't grow in a Petri dish culture as many are devoid of a cell membrane. As oxygen - meaning voltage - decrease in the affected cells and blood, these pathogen go from spherical to rod-shaped, to yeast-like to finally fungus with hyphae. First thing the MMS will do is go to the liver and the blood and get rid of these pathogens. Remember MMS is water-purification and the cell is 70% water as well as the blood. So, the MMS will start to give a chance to the immune system.

He can also do full body baths with 10-80 drops of activated MMS, and enemas with 10 drops in the future (300 mL of water, plain and simple).

If you decide for the MMS, yes, indeed watch out for those antioxidants that will neutralize it, and give him the antioxidants only at night.

So the protocol calls for hourly MMS doses and there is a reason for that. The MMS literally disappears as it reacts with pathogens in one hour, so the dosing needs to continue relentlessly.

Jemco:

I have, unfortunately, heard that story of yours repeated so many times, in a similar version, I mean.

I liked when you wrote: she was told by the "doctors". Theses are the people I am scared the most of. The combination of ignorance and arrogance, makes for a deadly cocktail.

Iatrogenic (doctor-related) death is the leading cause of death in the USA, period. This when you put together all hospital and drug-related deaths. It is really pathetic.

I volunteered at the Genesis II Health Restoration Centre in Bulgaria for two months in Feb/March this year.
I treated a Kenyan man with leaukemia twice a day for the three weeks he was there.
I applied a gauze to his spine and down the back of his legs to his knees. I then soaked the gauze in a CDS/DMSO mix using a syringe.
It was left on for ten minutes then I applied aloe vera gel to the same area.

Everytime he had this treatment he became very tired which shows it was working very well.

Hi Mike,
I agree with pejeal44. Try to get his dose as high as possible. And to keep the nausea down, I would recommend PAMMS here on the forum at:

g2cforum.org/index.php/list/general-discussion/26841-pamms-pre-activated-mms-9-17-2013

Or to activate the drops of MMS for 2 minutes using ideally 4% hydrochloric acid (or my 2nd choice would be 50% citric acid) instead of just 20 seconds.

All the best,
Scott

Rejuvinated blood using ozonated water plus DMSO in the skin..... MMS kills the parasite
Virgin coconut oil 2 tsbpn
Youre correct , ph body is very important to fight off the disease
Follow Pams advise on protocol
if everytthing else fails ...its in the patients resolve to live
The above had been effective to almost all that wants to live longer


this is how I treat my friends and anybody else that listen



Heal your inner mind and the rest will be cured let go of all the problems and the doctors away
its just like an excuse or reminder of how we abused our body


Im new to MMS and DMSO but they are surely an added bonus to have a quick fix on pain , recovery and budget constraints

In the Philippines,
We as traditional healers used only oil, water , and FAITH in God to overcome our miseries
Its up to the patient to help him or her to cleanse his body and soul

Hope for ur Dad's fast recovery

Thank you everyone for your advise. I would love to get him home and started on protocol 2000, but it looks like they are keeping him here till 10/5/2013 now. They found something in his lung and sent a camera down there and took a sample to see exactly what it is and treat it properly. Shortly after the procedure he went back into a fever. Last night he got back up to 103 but now is back to normal and just sleeping alot. If they can get ride of his lung infect, which they originally said it looked like a fungus pneumonia we might get out of here. This morning a doctor came and woke me up and said they are now thinking it might be a bacteria instead which would be easier to treat. He also has a blood clot in his right arm where they have installed a pick line. Today we get the resaults of the bone marrow biopsy to see what the chemo did and if his leukemia has some what been defeated. I'll keep everyone updated as I hate reading through this forum and coming across stories that never get followed up on. Thanks!


Oh, does anyone know if the MMS would conflict with the medicine he's taking? Thanks!

MMS should not conflict with his meds.
Pam