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genetic anomalies and mms1 09 Nov 2024 16:26 #84684

  • papertigers7
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We were introduced to MMS1 back when my mom had pancreatic cancer. Unfortunately, she passed away as the book we received was quite confusing and did not know how to mix it up. As her caregiver, I had so much brain fog and was exhausted from my issue and could not comprehend how to use it.

Fast forward, to this year. Our NP has been taking classes in MMS and suggested my father with prostate cancer (shared his story in another thread on topic), So her basic directions was easy to follow. I was born with a heart defect that required several surgeries to repair, ended up battling infections at times throughout my life.  On heavy antibiotics, affected hearing so have hearing loss.  Also on anticoagulants due to the mechanical valve put in.  

I had issues with a normal level on warfarin, so had it on low end. The anticoagulation clinic did not like that, so they discharged me.  Since I was discharged, just completely stopped warfarin.  Started using Nattokinase instead per Dr. Peter McCullough.  I'm adding in cayenne and lumbrokinase as well.

I was born with no thymus, so challenge getting infections out of system, and low functioning parathyroid glands.  I'm hoping that I as I continue on MMS1 hourly, it will get rid of the heavy metals, reverse the parathyroid gland dysfunction, and treat the lingering infections.  The only medication I'm on is for the parathyroid & calcium absorption issue.  I have been able to stay off all other meds, by focusing on natural options and doing research.  Also stayed out of the hospital inspite my calcium being low for a few years.
Dana W

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