TOPIC:

I live in PA in the USA. I was exposed to the rabies virus and have been symptomatic for 5 months. I have almost every rabies specific symptom. I need urgent advice from some kind of Dr on how to treat this with MMS. I’m not sure if I should start slow or treat more aggressively. Thank you.

I am not a medical doctor and I am not aware of any forum members who are medical doctors. As a MMS forum member I suggest two options:

1. Follow the HRP in Jim Humble's latest book, MMS Health Recovery Guidebook.
2. Follow Protocol 115 for Viruses.

Hello and sorry to hear of your condition - from what I've read, generally people who have rabies and develop the symptoms almost always die because by that time it's usually too late to treat it. So knowing that, if it were me I would try to knock the hell out of it asap because I'd be looking at a death sentence. And the best way I know to try to stop the disease asap is via an IV of dilute chlorine dioxide - either CDS or CDH - I personally would use CDH since I've already done it many times and there has never been a problem using it as far as I know.

On day 1 I would probably do an IV of 250ml of 100ppm CDH to hit it hard and then I'd probably do an IV every day for a week using 100ml of 100ppm CDH.

Ideally I'd want to be checking my hemoglobin and other blood parameters at least every other day (if not daily) to make sure nothing was getting too low.

This, I would think, would be my best chance at survival.

Here's where you can find my posts on the forum about going intravenous:
mmsforum.io/goto/cdh-research/30833-cdh-intravenous-injection-of-dilute-cdh-to-cure-infections-of-the-blood-appears-to-be-safe-and-very-effective

Hope that helps.

I hope you make it,
Scott

I have been symptomatic for 5 months. I am losing strength in my arms right now and can’t think straight. Drs would not listen and I have documented everything. I have tried to get help everywhere I can think of but no one will believe me since I’m the only one this has ever happened to apparently. I don’t understand why it progressed so slowly for me but I think that choke change the way I treat it . Thank you for the info.

If I were you and couldn't think well, etc., I'd at least try to get as much CLO2 into me as possible without making myself sick and throwing up. In order to do that in a fairly easy way, and to make the MMS more tolerable so I could consume more drops per hour faster, I would activate 3 drops of MMS with 3 drops of acid (ideally 4% HCl) for 3 minutes in something small/narrow like a plastic thimble or small bottle or test tube or if I didn't have anything like that then I'd just use the smallest cup I have and tip it sideways so the combined 6 drops will accumulate at the bottom and make a little puddle. I'd do it for 3 minutes instead of 30 seconds so that it will be more fully activated like CDH and therefore less likely to make me nauseated. This way I'd be able to take more drops and therefore get more CLO2 into my blood quicker. If I didn't feel sick after taking 3 drops this way then the next hour I'd increase to 4 drops and then 5 and so on until I found the amount that caused nausea and then I'd back down to the amount that didn't cause nausea and stay with that for as long as possible.

By the way, I would add at least about 60ml (2oz) of water to each drop of MMS activated in this way before drinking it down. So 3 drops of MMS activated this way would first be combined with about 180ml (6oz) of water before drinking - more water is okay too.

Another by the way. To make this easier to take and to reduce nausea, I would hold my breath while drinking the solution and then before breathing I'd chew up something small and sweet like a raisin or a chocolate chip. Then I'd breath. This would make this CLO2 consumption much easier to do.

Instead of activating hourly I personally would just make up a batch of CDH but if I didn't know how to do that then I'd do the above.

Hope this helps you and others who have muddled minds due to your disease and therefore have a difficult time doing the more complicated procedures we have here on the forum.

I write as to what I would do because I'm not a doctor and so cannot give you or anyone advice - I can say what I would do though. So there you go.

All the best,
Scott McRae