Comments on: Mistletoe as Iscador

By: Sherry

Sherry — Tue, 08 Nov 2011 06:03:42 +0000

Hi
I had Metaplastic Triple Negative bc. Mastectomy and chemo finished June 2011. My last tumour cell count showed 4.25 m potential tumor cells in my blood although we won’t know if they are active until my next test in January 2012.
From the moment of diagnoses I have been very proactive in staying well though nutrition, exercise and happy head work. I also inject Iscador mistletoe 3 times weekly. I live in Canada but have a wonderful ND who specializes in oncology and has hooked me up with the mistletoe. What I’m wondering is how long a person should be on it. For 3 years when my recurrance risk drops or 5 years when it drops again or is that too long or too short? Thanks for any advice on that you can give me.

Sherry

By: ProfKeith

ProfKeith — Sat, 15 Oct 2011 17:15:48 +0000

Well done Debbie!
Stories of grit and courage like this are great.

By: Deborah

Deborah — Fri, 14 Oct 2011 22:34:53 +0000

I was diagnosed with breast cancer between christmas and new year and the evening that I had my first scan and mammogram I happened upon the documentary ‘A World without Cancer” and knew straight away that the way that the doctors wanted to treat me was not right for me. I practically spent every waking hour googling natural cancer cures and came across Mistletoe therapy amounst other treatments.
I was a walking organic grocery shop with my phillips juicer.
Through my searches I came across Dr Maurice Orange clinic in Tonbridge Kent at the Raphael medical center and started Mistletoe therapy with him in February 2011
He supported my decision that I did not want chemotherapy or radiotherapy, but still said to keep an open mind about them. But I am stubborn and was adamant that there is a way to beat cancer without such horrible barbaric poisions.
I had the tumor injected and also had an IV of the solutuion.
I experienced the expected fever for about 3 days on the second appointment when I had my first proper treatment. The tumour also swelled and was very tender. But it didn’t scare me or freak me out. It was uncomfortable being very restless and sweaty for about 4 days and basically feeling wiped out, and during this very calm.
I had a series of treatments from February to May which was the last time I saw Dr Orange and I have had a couple treatments since he left with his replacement.
We couldn’t believe how much smaller the tumour had become and how fast.
My tumour was about the size and hardness of a walnut and now we could barely find it! I am thrilled.
BUT I did do all the other stuff too that you as a patient must take responsibility for.
DIET… juiced the shelves of waitrose dry,
I also follow the Dr Johanna Bugwig flaxseed and quark twice a day with juiced lemon, tastes gorgeous.
Alkaline the body and only eat organic, ( ok 90% is organic and yes I have cheated and yes I felt guilty). And I drink alkaline water and have a chansen water water filter.
I now inject myself weekly and my second scan showed the tumour had reduced from 3.5 cms x 2.5, largest measurement was 4 cms and could easily be found.
The shadow that was there is now 2.5 by 2 cms.
But I can’t feel it, and I am constantly feeling my boobs!
I am expecting some scar tissue from the tumour being injected but the ultrasound should be able to tell the difference between the two.
The NHS have not helped me at all, and basically discharged me ‘ treatment not needed” is what they said because I dare refuse their “gold standard treatment” and dare to question them. I requested a second appointment to see the first doctor in July and was told October, now its end of November. Just as well I am very happy with my informed decision not to allow them to poison and slash me.
I know that I will have to keep and eye on my illness for the rest of my life, and I will forever be grateful to Dr Orange and his small and dedicated team and they really are health professionals and Mistletoe therapy SHOULD BE AVAILABLE TO EVERYONE who wants it.
I could tell you all so much more about what I have learned , just there is soooo much!
Love to all
Debbie

By: cynthia Swan

cynthia Swan — Fri, 08 Oct 2010 03:40:46 +0000

Hi,
Wondering if you have any info about Iscador for Papillary Cancer patients? I am wanting to take it while I am getting my mercury amalgams out prior to the surgery of having the thyroid removed. I think there is a link between this cancer and all the mercury in my mouth. I am on a supplement, exercise and diet regime as well ovreseen by both my medical doctor and my naturopathic doctor. IscadorM was recommended by weleda. Can you shed more light on this? Can this be helpful for papillary cancer prior to surgery?
Any insights or studies would be most welcome.
Thanks,
Cynthia

By: Dr. Keith

Dr. Keith — Sun, 11 Jul 2010 18:57:33 +0000

I’m not allowed by my insurers to give consultations of the sort you ask. I notice you don’t mention diet, oxygen and other therapies. Iscador is not a panacea that can work all on its own. If you feel you need more education, consider my “Cancer Confidential” report:
http://www.CancerConfidential.com
Prof.

By: Sue Newton

Sue Newton — Sat, 10 Jul 2010 00:14:21 +0000

I have Stage 3B melanoma…5 surgeries in 2001-2002 on the breast…a year of interferon after that…after 8 years now it returned in the breast again in October 2009. Had surgery, clear margins, returned again March 2010, surgery w/clear margins, had surgery again yesterday July 8th, all in the breast continually moving to the left but still clear nodes at this point. Could Iscador help me and if so what kind. I was on GMC-SF for 6 months and was just taken off it because it was obviously not working.

By: Dr. Keith

Dr. Keith — Mon, 17 May 2010 14:34:45 +0000

Just don’t rely ONLY on Iscador and “stuff” Gillian. Lifestyle change, especially diet, are your key tools. Iscador is just an adjunct.
Prof.

By: Gill Anderton

Gill Anderton — Mon, 17 May 2010 10:17:13 +0000

I have been taking Iscador P3% sonce March 2010. I have had no side effects so tolerate it very well. This is prescribed by the Homeopathic Hospital in London. Unfortunately, my local oncologist from Christies in Manchester is less than enthusiastic about ‘complementary’ medicines and offers no encouragement at all. Despite my breast cancer being incurable and no western ‘scientific drug’ as yet has been found (despite the millions of pounds being invested in research) he can offer no alternative. Sadly, opposition will be found by those ‘blinded by science’. I feel generally very well and look forward fighting this disease with confidence.

By: Catherine

Catherine — Wed, 24 Feb 2010 10:03:28 +0000

I recently started taking Iscador therapy in drop form and have experienced stomach pain, nausea, headaches and vomiting. I am not on any other current treatment for cancer. I am not sure If have a stomach bug, or it is the side effects fo the treatment. Has any one else experienced this while taking the drops.

By: P.L.G.V.

P.L.G.V. — Tue, 29 Dec 2009 00:09:55 +0000

I would love to know of other Prostate Cancer patients taking Viscum Fraxini. I have been in that therapy for almost two years. plgv2000@yahoo.com

Best wishes and a healthy 2010 to all.