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Question about MMS- I'm new to the board.


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ashley
3/25/2011
9:35:50 PM


Mel, thank you. I had tears in my eyes after reading your post. I finally have hope that I'm getting some where with this disease. I'm so glad someone else has experienced what I'm going through now. I know that I still have a long way to go and as exhaused and tired as I am of the everyday fight, I will beat this thing no matter what I have to do. I have a beautiful 6yr. old daughter and a wonderful husband who needs me healthy again.
As far a the Wellness Protocal, I have not been able to afford it. I am trying to save for it but it might be another couple of months before I can purchase it. It's been really hard fighting this disease when I can't afford to get the things that I need.
I had to save for over 4 months before I could purchase the MMS, Molecula silver, olive leaf, and probiotics that I currently take now. I am also taking 'Alive whole food' multi-vitamins that a friend purchased for me. I know that the MMS is working but I'm still not sure about everything else.
I still have many 'cuts' on my hands, mainly fingers. I'm hoping these will go away soon.
Long road ahead of me...

Thanks again, Mel. You have truly been a blessing and inspiration to everyone on the board:)
God Bless,

Ashley


mel
3/25/2011
11:25:31 AM


Hiya Ashley,

Welcome!

Thank you for your kind words.

Hopefully your struggling is coming to an end.

As I have recently mentioned in teleconference calls, I never started bathing in MMS until I reached my maximum dose and started my maintenance regimen.

It is because of what you described that I recommend people doing it in a cautious way. I was afraid that if people saw what you and I have seen in our bathtubs they might faint. We have always said better coming out than staying in.

To ensure the best results, I must reiterate that it is not some of the parts, but the SUM of the parts. I hope you are also on the Burgstiner Wellness Protocol (along with the Ubinol CoQ10). To this day, I remain on it to keep my immune system strong and fully functional, and to ensure that I will never have Morgellons again.

Unfortunately for most, it will not be gone quickly. I stayed on my entire protocol for 18 months to ensure the total eradication of the disease.

Ashley, you are never alone when you are here.

I hope we helped a little today. If you wish to speak with me directly, my email address is in the welcome letter on the forum page.

God Bless, Never give up Hope,

Mel



Ashley
3/25/2011
9:35:50 PM


Hi Everyone!
I'm new here. I've been reading the boards over the past few months but I've never posted anything. I'm still trying to understand Mogellons. I've been struggling with this bizarre disease for over 3 years now.
Thanks to Mel, I have learned about the benefits of MMS and recently started using it.
I have had great results using it internally and bathing in it but I have a question about the results that I getting from it.
Has anyone else experienced an increased amount of fibers shedding from the body after taking each dose? When I say increased I mean that they do not stop coming out of my skin and scalp.
Also, I'm getting several of these parasite looking things in my bath water every time I bath in MMS. I know that they're coming from my scalp because they don't emerge until I soak my head in the bath. The strange thing about it is that with each bath I'm getting several different kinds/types of these 'parasite-looking' things. They're really creeping me out because I figured they would all be gone by now:(
Has anyone else experienced this while using MMS? I'm just hoping I'm not alone on this one.

Thanks and god bless,
Ashley