Riordan, Cameron, Drisko Protocols
other version from NewZealand: http://www.alternativehealth.co.nz/cancer/vitciv3.htm
Hi regarding Vitamin C therapy, it is not a cure all. I took IV vit C for four months at 100 - 150 grams a daily. Sometimes we had to put in through my feet as all the viens collapsed. My Ca125 rose from 18 - 2500 in three months.at first I was told that my scan had become clear with the treatment then we realised that they were looking at the wrong scan report. I was in fact coverd in tumours again. This was my third reoccurence in 18 months.
The vit C is contraindicated in abdominal tumours we have since learnt as it encourages ascites. I developed 17 pints of fluid and a blood clot nearly died, whilst taking the infusions. I came if the IV c and took chemo again ( 3rd course in two years). The chemo worked at first and now I'm on my fourth reoccurence in two years.
I had a friend who has since died who use IVC as well. She also developed ascites and fluid around her lungs.
I am married to a doctor so I was monitored and looked after wonderfully. Unfortunately IVC does not always work. Sorry to put a downer on this. I am now looking at NCD virus therapy and still praying. I am 26 months past my sell by date. Thanks to God and great medical intervention. Marian.
I tried to highlight the major findings. Colors: Frequency, Dose, Speed, Period, Supplements, Effect, Condition, Side-effects, Advice, Notice.
Hi, I just wanted other women like myself who have advance ovarian cancer 3C to know that IV vitamin C has helped to put me in remission. I took 100grams daily by IV from July 2006 - Sept and now my CT scan is clear. The scan report previously showed a tumour in my pelvic area 1.5cm plus substantial cancer on my colon (I already have a colostomy from past surgery for mets). I had already had two courses of chemo that had not worked and I refused the third course due to fear of felling so ill again. I took VPS and omega 3, salvestrol etc., a strict vegan diet with no sugar or yeast etc., and so far so good. Considering I was given only six months to live I am thrilled. I hope and pray that I remain clear as at one time my CA125 was 8500 (Jan 2005). I have been in hospital and a hospice for seven months which was terribly hard on my family. I have four children the youngest is only four. Please consider IV vitamin C if all else fails. ... Marian
If you add K3 and r-ala you can get a much higher saturation level with smaller amounts of IVSA and it will stay in your system longer. Don't forget your bindweed Vascustatin and imm-kine. The IVSA only kills around 65% of the cancer cells, leaving the more aggressive ones behind.(Hickney and Roberts) so you need your immune system to be in a good position to help to deal with the rest. These products really worked for me. They help to reduce vascular growth to the tumour.
I know that the finances or lack of them is a great worry but the alternative dosn't bear thinking of.
If you need any help with the IV protocol etc., please email me. I'm looking at the NDV vaccine now for ovarian cancer just in case. Also there is a lab in spain that will make a vaccination for your ovarian cancer specific to you. What direction are you looking in now?
Are you taking VPS and MorEpa? <- what is this? need to research further...
I far as I understand of what is does from the description on this page: Vascustatin inhibits the blood vessels growth. Also the page says: "Highly recommended for use in conjunction with Imm-Kine".
We did the IVSA every night in our bedroom using a very fast drip to get the high saturation levels that are needed. A slow drip did not work for me. 100grams over 2 1/2 hours. With r-ala and K2 and K1. The cost was about $1600 monthly due to the cost of the drip equipment and solutions but then again if someone had told me that if I was to pay $5000 and get well I would have thought the price was cheap!!
If the 50grams does not work and I know a few people that have not responded to it, try a higher dose at a faster drip rate. Marian.
To get the maximum tumour kill we used K1&2 or 3. B12 is also important. Go to vitamin c foundation for more details. You can download the different protocols as need be.
Everyone is different. Mine is an extremely aggressive cancer. My tumour marker can move from 7 to 1200 in two months. My highest figure was 8500.
I usually start the drip in the evening but at times when I have been really scared I have been on a drip round the clock. Vit C is non toxic so you do what you have to do to survive.
What stage are you at? Do you have any mets? Where are you based?
Wishing you courage and peace. Marian.