Mast Cell Activation Syndrome (MCAS)?

Does anyone else have mast cell activation? I have had it since birth but every since starting MMS I seem to have resolved my symptoms. I no longer have facial flushing or need to take antihistamines. Anyone else had this effect from MMS? I asked world MMS expert, Dr. Afrin about it and he never hear of MMS of course.  Thanks for any comments you might have.

Please tell me the protocol you did exactly. What form of MMS. What ingredients. I have this really bad. It isn't helping. Thank you!

Hey there, I have this. Just started the protocol and wondering how you are doing now? Thanks! 

I also would love to know what MMS protocol you used? I would love to have such a natural remedy. Thank you.

Happy it is working for you.

For others, I would say to simply keep at it.
It all takes time and you have to be consistent and get the Clo2 into you. There are different protocols but ultimately, more is more. Work up to it whatever protocol you use for MMS or CDS and keep adding more as you can manage and make sure you are not consuming anything that will cancel out the Clo2 or waste its energy (like eating vitamin C amongst others).

The more you clear out your system, the fewer problems of any name you will have.