The Universal Antidote“I have a British Isles complexion; fair skin, burn if I stay out in the sun too long. Due to previous sun exposure, I have what the dermatologist call ‘pre-cancerous’ skin lesions on my face. After a poster on here recommend misting the skin with ClO2, I have started spraying my skin several times per day with ClO2, and the lesions have either gone away entirely or are on the verge of disappearing.”
Protocol Used: CDS Spray Protocol D
“Quick bit about my asthma. After just a few weeks of protocol 1000+ I stopped needing my asthma steroid inhaler and other asthma meds. It’s been 3 weeks now and I’m still not needing them. Well today I was in an allergen situation that I could not tolerate in the past. Heavy pet dander for almost 3 hours. I did feel the need to use my rescue inhaler once at first but in retrospect it could have been that I was a little anxious to be exposed to the dander. I am now 2 hours removed from the environment and I feel 100% normal. I would normally have symptoms for DAYS after exposure. My mind continues to be blown. Thank you so much to this group and to the Natural Health Knowledge Groups for helping me on this journey. CDS for life! God is good. ❤️👏”
Link to original post HERE
Protocol Used: Starting Procedure and Protocol 1000
“Just wanted to say, I have used MMS on myself for 15 years off and on, but never tried it on my cats until I joined this group. So yesterday someone dropped off a kitten at our house. She was very friendly and thin and had upper respiratory infection. Very noisy breathing. I made up a 2 drop mms solution with a cup of distilled water and gave her small dropper doses over 4 hours. She readily drank the doses. Now she is happily indoors and breathing normally.”
Protocol used: Pet Protocol
“I just wanted to give a huge Thank You to everyone that has provided me with the knowledge and help that I have received since I first learned of MMS. I was diagnosed with Multiple Sclerosis 1 year ago this week and being only 25 at the time, it was a pretty upsetting diagnosis. My first 6 months or so after being diagnosed were pretty difficult and stressful. I had every symptom imaginable, from full body numbness to losing complete function in my arm and leg…to exhaustion and horrible headaches, memory loss and brain fog, electrical shock sensations running down my spine and through my arms and legs, and the infamous “MS Hug” –a horrible tightness/extreme squeezing around my midsection. I’m sure I’ve even missed some symptoms, but you get the idea. It wasn’t fun. After my first major “attack” or flair up I read that some people will have a flair up and then will get better and not have another one for years and years. This was not the case with me. In 6 months I had been hospitalized once, had to relearn how to walk and tie my shoes and get dressed, had to administer my own IV at home 2 times (3-5 days each time) and had 3-4 more attacks. It was an incredibly un-fun rollercoaster.
In July I began taking MMS. Shortly there after my hands which had been numb pretty consistently since Nov. 2011 began to get feeling back. My handwriting started looking more like a 26 year old and less of a 5 year old. I was able to type for longer than 3 minutes at a time. I have now been taking MMS for a little over 4 months and as I type this tonight, without jinxing myself, the only symptoms I am still experiencing are extremely mild numbness in ONE finger on my left hand and occasional fatigue. I am baffled. I cannot believe that the symptoms that plagued me continually for 6 months have all but vanished. I am so eternally grateful for everyone that helped lead me down this path. I can’t say that I enjoy the taste of it with the high dosage that I need to treat the MS, but I will take the temporary awful taste any day over my lasting symptoms from before.
So anyways, this is just me saying THANKS! And I definitely would recommend doing your research if you have MS and are not happy with your current treatment as this might be something that can help you out as well!”
Protocol Used: Starting Procedure and Protocol 1000
Curious outliers comment:
If I had multiple sclerosis, I would also look into high dose vitamin D therapy. High dose vitamin D must be taken with its cofactors also. Vitamin K and magnesium.
This testimonial was shared directly with me from a person in the private chat group.
“Good morning Curious Outlier,
I have some interesting info for you. Yesterday was my 9th day of the protocol (I backed down to 2 drops for 6 hours this week, it was to intense) I started nose drops I accidentally used 2 drops per oz. not 1. not sure if this did it or it was a combination of both but….I can smell this morning!!!!!!! After 6 weeks
Not saying this will work for everyone. We are all different but the clearest improvement I have had so far. 🙏
God is amazing!! I prayed about it yesterday morning, And then I made that mistake with double drops. I have been through the material and videos numerous times. I even strung together lessons one through seven to make one video so I could listen in the car. I couldn’t understand how I could have made that mistake. Gods hand at work totally 💯 🙏🙏 Just As he is working through you! Blessings to you CO
Just wanted to share
Justice
Protocol Used: Starting Procedure and Protocol 1000