MMS , Skin Rash/pus and Candida Re: MMS and Candida

[Guest guest]

Hi I'm new to the group. I had planned on lurking and learning for

while, but hearing that there are others experiencing the painful skin

rash and pus that I had. I'm not good at being technical about this

stuff, but through research I have figured out how to get rid of it or

at least control it. From what I understand, you body is trying to

expel the toxins - in this case, candida. When you do it faster than

your body can rid itself of toxins, it manifests itself as headaches,

nausea, worsening symptoms and this skin condition.

I did not what to slow up my treatment, so I researched other ways to

cope with the symptions. The following are things I tried that have

alllowed to to control and frequently rid myself of those symptoms

Spanish Black Radish, Charcoal pills, bentonite, and periodically I

take a baking soda/ organic lemon juice solution

I have not done it often, but I have read that coffee enemas help.

I've also read the vitamin C flushes can help, but I have not tried

that as a solution for this problem.

When it went away, I stopped taking them and four weeks later it came

back. So, I started taking them again, except for the baking soda and

within three days I started to see the symptoms recede. The pain was

gone.

Tracey

>

>

> I get something that is possibly a yeast thing being drawn out

> through the skin no matter what treatment I've taken, including

> MMS. It's a greasy, smelly sweat which burns the skin quite

> badly. I don't sweat at all otherwise so this is not a normal

> sweat. It only ever appears in the creases of the body where it's

> harder for something to dry out, arm pits, under breasts, etc. It

> clears up in about a day with Nizoral 2% cream and putting a tissue

> or soft cloth over it to stop the excretion staying on the skin, and

> it doesn't come back again for a while. I suspect that it is

> happening in other sections of the body but because the air gets to

> those easier whatever it is coming out, doesn't get a chance to burn

> the skin. After I've been on whatever treatment I'm using at the

> time, it stops so I guess a point is reached where it is either gone

> altogether or is not so abundant that it can't come out via other

> excretion pathways. I have lymphedema in the legs so perhaps that

> contributes in some way. The lymphedema is thought to be due to the

> large cysts on my ovaries blocking the lymph flow so I don't know how

> that affects the rest of the body.

>

> Best wishes.......LD

>