Mother, and nurse who carries out the procedure of giving cancer patients chemotherapy, refuses to give her own child chemotherapy at home…
In this email she tells her story…
“how ironic is it that I prescribe the very same meds to others in the past and now I have made a decision that MEDS JUST SLOWLY KILL US. They don’t help us, doctor prescribe meds because we get a cut out of it from the pharmaceutical companies.” – Sonia C.
THIS IS WHAT MOST CHILDREN LOOK LIKE 7 MONTHS INTO CHEMOTHERAPY.
THIS IS SONIAS DAUGHTER, BRIANNA, 7 MONTHS INTO HER CHEMOTHERAPY.
Here is some light history about our family, and Brianna.
Brianna was diagnosed Sept 28.2011 with ALL Leukemia-standard risk. She was admitted into the hospital and stayed as an impatient for 6 weeks. When they first diagnosed her the hospital staff didn’t give my husband and I even 1 sec to process the word CANCER let alone our 2 year old having it. It was an extremely devastating time for all of us. Even more so for me because during her admission as I was almost 3 months pregnant.
Brianna was discharged home October 29.2011 and it was her first week at home that my mother mentioned Paul Beattie’s name to me. As soon as she did I called him at 930pm and he returned my call almost midnight. The first convo was very difficult for me to speak to him because I was ready to sell my soul to take away what my daughter had and give it to me.
That is when he told me get rid of all chemical products/cleaning/washing/refreshers//and put her on cod liver and Efamol and a children’s multi vitamin, and give her Epson salt baths 2 times a week to balance her magnesium levels. Stop buying food at the grocery store.
The next morning that is exactly what I did. Jan 24.2012 Brianna did a bone marrow and the results were astonishing. In 100 billion cells not 1 cancer cell. So crazy to believe 1 week later the oncologist requested another bone marrow done, with the exact same results. How is it this child after less then 4 months was cancer free but yet still had to follow protocol and receive chemo for another 2 years. That’s is when I stopped giving her chemo at home. Most people that would hear me say this including family and friends would think what kind of mother am I?? I’m taking a chance with my daughter’s life?? NOT at all, doctors follow exactly what they study in school. I’m speaking with experience as I’m a nurse practitioner, and how ironic is it that I prescribe the very same meds to others in the past and now I have made a decision that MEDS JUST SLOWLY KILL US. They don’t help us, doctor prescribe meds because we get a cut out of it from the pharmaceutical companies. Every med filled out by me and taking by a patient is 25-40% more moola in my pocket.
Shocking Hmmm?? Bet u didn’t know that.
Here we are now April. 28th 2012–my daughter has been undergoing chemo treatment for 7 months none, which she has gotten at home…but the worst of it, is being given to her at the hospital. Still looks like a regular kid. No hair loss no grey color, no weight loss, no loss of energy, no loss of appetite. And all the oncologists are scratching their head.
Just this week I’m been asked to give consent on having Brianna DNA tested. Stupidest thing i have ever heard. I have told them time and time again it has nothing to do with her DNA. She isn’t super woman-or amazon princess. She is no different then any other kid. But what she does have that no other kids parents are doing is giving her fatty acids that her body was previously lacking and she is jacked up on it and is healthy and strong like a horse. NO ONE CAN FIGURE OUT WHY!!
Now you may be wondering why doesn’t other parents do the same to there kids or why doesn’t the hospital make sure all people take these EFA’s ill tell you why.
Cod liver -Efamol doesn’t make pharmaceutical companies and doctors any MONEY!! that is the bottom line. Next question why don’t other parents give this to there children, or parents, friends..etc… Because they put all their trust and faith in doctors when doctors DONT CARE UNLESS IT MAKES THEM MONEY. Hard to believe because the truth hurts.
I as a mother will not nor will I ever put my daughters life in anyone’s hands except my own. Because I know the pain I had to go through to bear her. Its because of these EFA’s that my daughter is alive and has beaten cancer months before her time. Nothing to do with the doctors nothing to do with the chemo because those supplements are so powerful that they have fought off all side effects of those poisonous drugs. I love my baby too much to kill her slowly.
here is a recent photo of her. I bet when you look at her not one person will believe she has chemo running in her blood day in day out. because she doesn’t look like a “so called” cancer patient.
Best wishes Andrew.
I have attached 2 photos first one is Brianna 7 months in treatment with ALL leukemia standard risk
second photo is a girl 1 year older then Brianna 7 months in treatment with ALL leukemia standard risk
you can obviously see the different EFA’S do