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Let me introduce myself: I am 58-- living in Calgary Alberta, Canada; I am a wife, mother and a grandmother. I am a Chocolatier—had just finished with all the education and was looking forward to starting my new adventure when within a month I was diagnosed with Breast Cancer.
I have invasive ductile carcinoma—stage 3—was diagnosed in November 2011
I had a triple biopsy, 2 in the breast and 1 in the lymph node—all 3 came back positive
Here is my journey since day 1
Treatment suggested: (in that order) aggressive Chemo, radiation, surgery, hormone treatments and possibly more chemo and radiation—before any treatments, doctors were already talking about reoccurrences. I was told without this treatment I have 12 to 18 months to live (In my heart I know I would already be gone if I took their treatment.)
I’ve watched too many people around me die after results from Chemo treatments and decided to do alternative medicine. I no longer have my family doctor for advice for she was in full disagreement with me –now I have an appointment April 19 2012 for another ultra sound and if there is no improvement, the cancer clinic wants my decision for treatment on May 9th 2012.
The most difficult part of my journey was to convince my family and friends of doing alternative medicine. Now I have them on my side.
Like most of us, I don’t have the finances to go off to some clinics for cure so I did my research (somehow I missed the MMS cures)
Alternative treatments tried: 42 day fast (juicing—to starve the cancer) (unsuccessful—had to stop for blood pressure crashed and could not sustain it any longer.
I was also on the Aloe juice by Father Romano Zago—stopped 3 weeks ago -no changes (may have helped by keeping it a bay, but shows no cure as suggested—followed protocol to the letter)
Followed the Budwig diet--Then went on a Macrobiotic diet—avoid all sugar, flour (as according to Budwig, most Cancer patients have low tolerance for wheat products or have Candida)
I take Colodial silver—vitamins –Eassiac tea ( note—can be really hard on the liver—over detoxing—I now take 1oz x2 per day instead of the 2-4 oz as suggested)
A friend of mine found out about MMS1 and brought it to me about a month ago and I was able to take a max of 12 drops per day. I was finally able to find a high quality of product to make MMS 2 capsules—started this treatment 3 days ago and already noticed less pain in the breast, but more pain in lymph node. I am taking the 1 drop per hour x10 hrs--and 4- ¼ capsules—hoping to increase in a day or two. I have to be cautious for I just got rid of a bad cold and before that I had a bad battle with shingles…so battling these left me quite weak.
I started also in the past month to see a healer (Shaman)—she’s wonderful—she is helping me rebuild my energy—as well as tested MMS1 through Kinesiology and through the testing found out it is very strong for me and advised me to go ahead and take it (note: she did not know what it was and when I told her after the testing—she still gave me the go ahead) we did not do this for MMS 2.
She also was the one to recommend the taking less Eassiac tea and added taking lemon juice instead.
Note: suggestion for those who are suffering with pain and also help in calming the liver—do the Edgar Cayce trick—castor oil pack and heat treatment—I know, it has helped me. Here in Canada it gets so cold and I’ve suffered with the tumors getting so hard from the cold, and that treatment has worked wonders on calming the pain. www.earthclinic.com/Remedies/castor_oil.html
In the last 2 days I’ve been reading your wonderful forum and decided to join, not only to get help but to be able to help others, if I can, through the knowledge I gathered along the way.
If anyone has suggestions to help me, it would greatly be appreciated.
Thanking you in advance for your help
Anne

Welcome, Anne! You are definitely a fighter! Please keep us posted on your journey and don't hesitate to ask any questions you wish -

Welcome to the best forum for MMS, Anne,

And thanks for sharing your journey with us. I too was given a grim diagnosis early last year and opted instead for quality instead of quantity of life and as it turns out I think I've gotten both!

I'm just now re-starting my battle and am planing to use CDS as well as MMS1 and MMS2. I went the route you took with some of your modalities listed, but found my trust wasn't in them, not that they were bad or wrong for some, but I felt something else needed to be done.

Looking forward to more posts from you and a long life for both of us.

Namaste

Cricket

Oh and thanks for posting the link.

Thank-you for your support- it feels so good to talk to someone who is taking the MMS protocols, for i have only told 3 people what I am taking.

Cricket,
Thanks for the support.
I am in this battle with you then, it makes me feel that I am not alone--for I did not join any other group for support. To say the least, this feel so right.
Cheers to MMS and a winning team!!!
Now, I'm heading for a MMS bath--1st time--such good info on this forum, only wished I found it sooner...better late than never.
Anne

Welcome Anne!

Will be looking forward to reading your progress in the coming months. Thanks for sharing and all the best to you my dear.

Welcome Anne, I'm so glad you've found the forum! It's such a beautiful haven of health and healing... truly thrilled to have you

Happy healing,
Jill

I'm also happy to have the support. I did give notice when I first found out about the dreaded "C" (which I don't claim as "mine") to my family and friends to please refrain from thinking of my demise or of me as sick, but instead to only have thoughts that uplift and are positive. So far so good.

You can probably read my post of my journey here, I think I listed the subject as "my story and I'm sticking with it", if you're so inclined.

Cricket

Hi Anne. Welcome and thank you for a comprehensive report! Please keep us posted. There are no coincidences in life!