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Does anyone here have mast cell activation syndrome? (MCAS) 16 May 2022 00:00 #75190

Maux52 Topic Author Offline New Member Posts: 3 Thank you received: 2	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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Does anyone here have mast cell activation syndrome? (MCAS) 30 Jul 2022 09:57 #76331

BillPopMMS
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Posts: 1092
Thank you received: 364

This is the reply I made to your previous inquiry. (for people who only see this post)

I had some time, so I am going back through the forum to see
if there are posts that no one commented on, and making comments
if I think I can offer something of value. I don't like to see people
"ignored" (not purposeful, I'm sure) when they are asking for help and such.

I didn't know about MCAS, so I had to look up some information on it.
There are SO MANY of these illnesses and diseases and syndromes
it is "ridiculous".

en.wikipedia.org/wiki/Mast_cell_activation_syndrome

Since it tends to be chronic, is an immunological condition, and is multi-systemic,
my 'guess' is that it is toxicity based or instigated. (as MANY illnesses and diseases are)

I wouldn't be surprised if your issues were due to childhood vaccinations,
which work well for most people (babies and children), but really mess up and
hurt others. (those that maybe are already toxic from their mothers and/or have a
weakened immune system that cascades into increased toxicity and ill health)

So it would not surprise me if MMS (detox) helped you with Health Restoration.

Once you get rid of the "toxicity" (the many forms that can take), your body should
generally just "fix itself". (most of the time)

How are you doing? Better, I hope, if not 'well'.

It's always nice for people to come back and tell us that they are achieving
good results so others who read the forum find good testimonials and
encouragement and positive information.

NOTE: Any and all information supplied in online or offline communications that pertains to,
mentions, replies to inquiries about, and/or involves a discussion of, the information on my website,
ASpoonfulOfMedicine.com, falls under the Disclaimer on my website.

CHP – The Clean Health Protocol
www.ASpoonfulOfMedicine.com/

You will find info there regarding Jim Humble's "MMS Health Recovery Guidebook".

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Last edit: by BillPopMMS.

Does anyone here have mast cell activation syndrome? (MCAS) 09 Oct 2022 03:45 #77020

wbamert
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New Member
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Thank you received: 0

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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Does anyone here have mast cell activation syndrome? (MCAS) 12 Oct 2022 12:19 #77071

runningmyrace
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Junior Member
Posts: 31
Thank you received: 5

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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Does anyone here have mast cell activation syndrome? (MCAS) 10 Dec 2022 12:25 #77103

BillPopMMS
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Platinum Member
Posts: 1092
Thank you received: 364

There were some problems with the forum that are corrected.

How are you doing?

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Does anyone here have mast cell activation syndrome? (MCAS)

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