Actual people

I am 67 years old and diagnosed 4 years ago with stage 4 metastatic breast cancer. I had cancer in my breast, back and ribs when I had treatment with zometa (a bisphosphonate) for 9 months to help repair my bones. The only other treatment I have ongoing is Letrozole a cancer drug every day. I have a very healthy diet with no red meat, no dairy products and large amounts of fruit and veges with fresh juice and smoothies. I had a hip replacement prior to my diagnosis 2014, and another hip replacement early 2016

February nine years ago I had my right eye removed because there was a melanoma in the back of it. I started taking TBL-12, now my 6 monthly visits to my specialist for checkups have shown that everything is healthy and these visits have now gone to every two years.

Hi.  My name is Sonya and I was diagnosed with Stage 3C High Grade Serous Primary Peritoneal Carcinoma in July 2015. I was also diagnosed with the BRCA1 mutation in May 2016. In the months leading up to July 15, I was slowly filling up with fluid in my abdomen and feeling very unwell.  I had been diagnosed with sarcoidosis in 2013 (auto immune disease) and my doctor originally thought it was the sarcoidosis causing the fluid.  I had an hysterectomy and  a cancer debulking  operation in October 2015 and then started six rounds of chemo.

I first took TBL-12 from Sept 2009 to Dec 2011 to reduce a high PSA level and stopped when it came down. This year i had an operation to remove bowl cancer, and feeling if I had stayed on TBL 12 it would have probably saved me an operation.

I was diagnosed with a right frontal brain tumor in 2012 following a double seizure at home. We found TBL-12 which according to clinical studies had immense healing properties and no known side effects. My last scan was November 2013 it showed no progression of cancer.

On 11/12/2016 our lives changed. Totally and forever. Everything that was our lives up until that day was instantly ripped away. That was the day our then 5 year old daughter was diagnosed with DIPG. Diffuse Intrinsic Pontine Glioma, a highly aggressive cancer of the pons. This is the part of the brain that controls all function like breathing, heart etc. It is also virtually inaccessible and untreatable. We were told that apart from radiotherapy there was nothing that could be done, at best a few months is all she has. That’s when we began to look around and do our research.

In 2014 Sophie  was 12 when diagnosed with conjunctivitis by our doctor. A week later Sophie could not stand any light at all and was wearing sunglasses continually.  She was also experiencing sharp pains behind her eyes.  I took her  to the emergency  department where they completed a lot of tests including an hour long MRI. I had to put eye drops (steroids) every 10 minutes into her eyes so she could open them for the doctors to look at. They told me her eyes  were very inflamed and she could lose her sight.