I’ve been diagnosed with Raynaud’s disease for more than x 10 years. After 3 months of 8 doses/day of CDS + unactivated MMS, I can now for the first time in years use my own fingers to type on a screen because the blood flow is sufficiently elevated in my extremities.
My usual dose was between 20-25ml CDS + 12-15 drops MMS in 1L of water- Protocol 102A. I drank 125ml every hour x 8 hours per day. I usually took a binder cocktail of 1T diatomaceous earth, 1 tsp Zeolite and 1 scoop of modified citrus pectin (Pectasol) in 1oz of organic apple juice and 6-7oz water 90-120 minutes after my protocol was done for the day. I could not tolerate MMS1- nausea and vomiting, although I did do it for 21 days earlier this year.
My fingers now work better than a stylus- prior to ClO2 therapy they would not register on touchscreens at all.
After 3 months on this dosage, I moved on to a maintenance dose of 3 hourly doses in a total of 12oz of water, 10-15ml of CDS 12 drops unactivated MMS. I do this daily because I do not want to lose my gains. I take this 2 hours after dinner at approximately 8, 9, 10pm followed by just the Pectasol at 11:30 and melatonin at 12:30.
