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Urgent ! Need help with my dad with MDS related Acute Myeloid Leukemia 24 Sep 2013 08:34 #36162

  • pejeal44
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Years ago, I studied under Hanna Kroeger. Leukemia was her specialty, as she worked in a hospital in Germany which took groups of patients in for 2 weeks, and they all left without leukemia, and never came back. Adjusting the tailbone:

Technique to set tailbone for leukemia - Hanna Kroeger: Google it, it is in You Tube

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Last edit: by pejeal44. Reason: http://www.youtube.com/watch?v=MRYX5D6ZlcA

Urgent ! Need help with my dad with MDS related Acute Myeloid Leukemia 24 Sep 2013 11:08 #36164

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Mike wrote: I just hope my dad has a chance to get back home at least one last time before this hospital keeps him for good. I know these doctors or going to just end up killing him.

You are very correct, if your dad stays in the hospital, more than likely the doctors will finish him off, as this is quite common. It happens to thousands monthly in the USA. Hospitals are quite dangerous places.

Allow me to briefly write about a friend of mine that was recently murdered in a hospital here in South Florida. Is murder too strong a word? Judge by your self. I call it murder by ignorance and apathy.

He was 61 and an outstanding international pilot, but contracted prostate cancer with metastasis. The first round of chemo made him very sick. Cancer went on "remission", he somehow recovered and started flying again. Cancer returned. A second "oncologist" told him the first chemo was not the proper one, so he prescribed another type and doubled it up. The side effect made him quite sick, worst this time, he was never prescribed or warned about clogs, and developed one in his right leg that traveled and lobed in his lung. He could not breathe well and went into the HOSPITAL. That was it. They did a tracheotomy and from then on it went downhill. His wife told me alarmed he was having seizures. I inquired about his diet. They had him in a high protein diet through IV plus albumin (egg protein). It took me 5 minutes on the Internet to realize this diet in a non-moving person has raised his ammonia blood level and created uric acid as it had overloaded his liver, affecting the brain. Indeed his ammonia went through the roof. They added more and more drugs to his IV. Anti-seizure, the oncologist, the urologist, the brain doctor added, you name it. At the end the cocktail was over 19 different drugs. Did they get together to check on any synergistic effect among these different drugs? Not that I know. Result, finished, kaput, in 10 days since the day he entered the HOSPITAL.

Death certificate: Cause of death lung embolism. REALLY? What about dead by chemotherapy and blatant ignorance?

So, I was diagnosed with melanoma, stage IIIb (whatever that is, I don't care). They wanted me on Interferon. I researched that. No way Jose, you do that to your mother, if you want to. I refuse to become some hospital's or doctor's guinea pig with some catheter in my jugular vein and being sick all day. I will go to my room at home and commit Seppuku if needs be, or die on my terms. So I got busy. MMS all the way. Mark in Thailand recovered himself from Melanoma Stage IV with MMS1 and MMS2.

Is MMS toxic? Does it kill you? Ha, ha. I was taking 15-20 drops hourly plus a whole capsule of MMS2 every 2 hours for months, whole body MMS and DMSO baths, and MMS enemas. It pickled me. Not a pimple anywhere. Colds? What's that? I injected the MMS in the melanoma on the foot, then used black salve, then injected it with hydrogen peroxide. I became a health minister with the church. I am going to Puerto Vallarta to become a teacher on November 3rd. All along, a surgeon is pushing me for more surgery. I rented a PEMF (pulse electromagnetic field therapy) machine and started "electrocuting" the cancer. I eat whole foods from an Amish Pennsylvania farm. Yes, lots of fat, like Mark Grenon boats about. It is good to make new cells. I feel great.
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Urgent ! Need help with my dad with MDS related Acute Myeloid Leukemia 27 Sep 2013 02:50 #36235

  • MikeAML
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Ok, we did the Hanna Krueger technique on him today. I had my sister who is a "licensed massage therapists" do it. Cant lie, I feel like she didn't learn it well anuf in advance or take the whole thing very seriously. None the less we did exactly as the video showed. I will be doing it to him a few more times myself until I feel its been done right. Well so far so good. His white cells are coming back up, same with his neutrophils. Platelets are increasing on their own, same for the red blood cells. The bone marrow biopsy resulted in 1-1/2% blast cells down from 70%. He's actually looking a lot better after the chemo. They had to take out his "pick line" that was in his right arm after they found a blood clot. They installed a new "hickmen line". They got him on blood thinners to keep the blood clot from growing and to help it dissolve. They plan on giving him chemo again in about 2 weeks, another bone marrow biopsy sometime next week and hopefully send us home tomorrow or the next. Still dont have an exact plan as far as the MMS is concerned. I'll likely start with protocol 2000. Anyway just wanted to give everyone an update and thank you all for your help.
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Urgent ! Need help with my dad with MDS related Acute Myeloid Leukemia 27 Sep 2013 14:49 #36255

  • Healthycelf
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There is another very simple treatment for blood clots, another for blood thinning, another for blood thickening (in case of bleeding from a wound such as a gunshot, which saved many lives in Vietnam) You might want to see if it's also on you tube under Hanna's treatments.

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Urgent ! Need help with my dad with MDS related Acute Myeloid Leukemia 29 Sep 2013 03:55 #36332

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Ok, so we made it back home! I honestly wasn't sure we would make it back after a few of the episodes I witness with my dad. Here's what happening now...

His blood counts are finally for the first time in about a year starting to increase on there own. They want him to go back for another Bone Marrow Biopsy on Wednesday or Thursday. Once they get the results of the Biopsy they are going to determine how many more rounds of the CPX trial Chemo they want to give him. For the record they gave him three rounds originally. They are talking about giving him more rounds of Chemo as soon as 10 days from now.

Here's what they got him taking as of right now...

Amoxicillin/Clavulan 125MG (1) at 9am and (1) at 9pm

Acyclovir 800MG (1) at 9am and (1) at 9pm

Voriconazole 200MG (2) at 9am and (2) at 9pm

Lovenox Injections (1) at 9am and (1) at 9pm - Lovenox is a blood thinner for his blood clot.

Terazosin 1MG at 9am - to help with urination.


I'm thinking that I should start him off with a half drop of MMS tomorrow (Sunday 9/29/13) each hour for 8 hours. I'm thinking I should start the MMS at 11am 2 hours after his pills and injection, and stop the MMS at 6pm 2 hours before his next pills and injection. Monday I'd like to bring him to 1 drop per hour, Tuesday 2 drops per hour and 3 drops per hour by Wednesday.

They say that originally his Blast Cells or cancerous Cells were 70% of his blood cell. After the first 3 rounds of chemo they now say its down to 1-1/2% Blast Cells. I would like to attack the Blast Cells with the MMS while they are down and try to eradicate them or keep them low anuf that when they do the next Bone Marrow Biopsy they decide that he's doing pretty good and maybe they will hold off on more Chemo. I know the MMS probably won't work that fast with the short amount of time I have before they decide to do Chemo, but I'm hopeful that it will.

They have been giving him a blood thinner through IV while we were in the Hospital. And while they were giving it to him they would take his blood every 12 hours or so do determine if they were giving him too much. They slowly decreased the blood thinner until they were satisfied that it was a safe number.

My MAIN concern at this point is that I remember reading that MMS acts as a blood thinner. They are very worried about him having internal bleeding as a result of the blood thinner they now have him on which is Lovenox Injections. They said if he gets any unusual head aches to call them up right away as it could be internal bleeding in his brain or something.

Will the MMS put him at a higher risk for internal bleeding with him on this Blood thinner for his Blood Clot in his arm?

Also, if you all feel that it is safe for me to give him the MMS, would you recommend something different then my plan? What about the MMS2 and the DMSO spray? How would you go about doing this if you felt it wouldn't put him at a higher risk of internet bleeding due to thinning his blood out much.

We also intend on going to the Dentist Monday or Tuesday while his WBCS and Platelets are up and taking out one of his back teeth. Reason being is they originally thought the tooth was responsible for the initial fevers that landed us in the Hospital for the last 2 weeks while he was Neutropenic from the Chemo. If they are going to do more rounds of Chemo we want the tooth out before they kill off all his Blood Cells again. Just a side note.

Thanks again to everyone here!
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Urgent ! Need help with my dad with MDS related Acute Myeloid Leukemia 29 Sep 2013 06:41 #36334

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I'm thinking, his body doesn't have enough time, in two weeks, to heal with the MMS, even if the MMS works on target. (MMS does not do the healing, it just helps the body destroy the pathogens, and your body does the healing.) You asked, so , I would keep with the tail bone adjustments, and the count will be normal in a week, like Hanna said in her "YouTube" video (if you watched hers,) "You cannot, cannot fail with this." Fortify the blood with the juices and egg if you at all can get by with that in the hospital. If not, wait until he get's back home. Chemo is very destructive, and I'd ask them to test, the day before the Chemo is to start again if possible, or hold off on it, even. Jim Humble, says that MMS will not undo Chemo damage, and that Chemo kills people, not the cancer... It is, your call.
God bless your dad, and you, as a family member. Keep us posted, as we all will learn from you.

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Urgent ! Need help with my dad with MDS related Acute Myeloid Leukemia 29 Sep 2013 13:58 #36336

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MMS will not put him at a higher risk for bleeding, Mike. It does not work as a blood thinner.

Check with the dentist re: an extraction with a lot of blood thinners - just a thought.

Your plan sounds like a good and reasonable way to start. Jim always says start low and go slow.

Prayers for your dad!

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Urgent ! Need help with my dad with MDS related Acute Myeloid Leukemia 29 Sep 2013 18:58 #36348

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Thanks Pam. Intend on taking him off the blood thinner the night before we goto the Dentist and putting him back on them later in the day after the extraction....thanks for your prayers!

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Urgent ! Need help with my dad with MDS related Acute Myeloid Leukemia 30 Sep 2013 00:56 #36358

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I have a bit of experience with terminally ill patients in hospitals. You need to take him out of hospital...even if it means signing indemnity forms. Then you need to stop all medication...simple as that. If a patient is dying anyway on a dozen meds...you need to stop them all. If they can eat, are going to the toilet, talking and hearing and seeing, they have a fair chance. Even severe constipation..which is a common side effect of hospital meds...can kill them. The side effects of so many meds usually kill the patient. Once they are out and eating and functioning you apply a tested protocol like MMS, or colloidal silver, or DMSO. Slowly. Then you mitigate the huge detox that usually results ...a zapper works well for this...but the MMS can handle itself. Then you work on their energy..orgonite, or geopathic and electromagnetic stress. Sunshine, walking, earthing. Then they have a fair chance. If they continue to stay in hospital their chances of making it are diminished each day. You have to just bite the bullet and ignore all tests and stuff...especially if they are dying anyway. I have had the best success with those that were palliative and told there was nothing more that could be done. Best of luck.
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