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Does anyone here have mast cell activation syndrome? (MCAS)
- Maux52
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16 May 2022 00:00 #75190
by Maux52
Does anyone here have mast cell activation syndrome? (MCAS) was created by Maux52
I have had mast cell activation since birth and it causes skin urticaria rashes, irritated dry skin and facial flushing. But, ever since I started taking MMS my skin had healed up and I no longer get facial rashes each evening. I am wondering what it is exactly that helps MCAS?
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- wbamert
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09 Oct 2022 03:45 #77020
by wbamert
Replied by wbamert on topic Does anyone here have mast cell activation syndrome? (MCAS)
So I am currently being tested / treated for MCAS. I plan to give MMS a try to see if it helps. I also have Lyme and the antibiotics have damaged my gut. Anyway, In doing research on MCAS, it seems that many of the issues stem from the gut. So issues like parasites, candida, leaky gut, over growth of bad bacteria can cause MCAS. So MMS would kill bad organisms in the gut and thus grant you relief. In addition to those, I just had a bad reaction to an antibiotic, which can also cause MCAS. So I am treating with MMS and a leaky gut diet to heal my stomach.
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- runningmyrace
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12 Oct 2022 12:19 #77071
by runningmyrace
Replied by runningmyrace on topic Does anyone here have mast cell activation syndrome? (MCAS)
After you use MMS to rid the pathogens, urine therapy may be helpful to rebuild the tissues. There is a really fantastic book called "Your own Secret Medicine" that I have referred to for many years and have used many of the different protocols although I do not have experience with MCAS. However, there are testimonies of everything from skin rashes to cancer being cured. Dr, Edward Group has some recent things online too if you search. He also recommends the book I mentioned above. Just another option to consider if you find you still have healing to do after MMS.
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