29th December 2014 – Update on my Cancer journey

Hi Folks,  hope you’ve all been enjoying the Christmas festivities. I thought it may be time for an update on my own cancer journey… Before continuing, can I please just mention that when I posted in September about my first salve treatment I was inundated with literally hundreds of questions and requests for advice. I apologise for being late in replying to some of the messages, or some that I may have missed altogether. At the time I was totally overwhelmed by the response. If, further to reading this post, you are seeking an urgent response please mark your query as ‘Urgent’ and I will endeavour to reply asap. I do however need to state that I am not in a position to give medical advice, but am happy to share my story with you, in the hope that it will raise awareness about natural cancer therapies, and that it may help you or someone you know who may have been affected by cancer. If you are contemplating using black salve, or other natural treatments, I would suggest that it should be done under the guidance of a qualified, experienced medical herbalist/naturopath. If you plan to buy black salve on the internet or otherwise, I would suggest that you are confident that it is from a reputable source. It is likely that additional products may also be required, such as drawing ointment, yellow salve, poultice powder, healing ointment, anti-scar cream. I would also suggest that black salve is not considered a treatment to be used in its own right, that would be the equivalent of having just the surgery but no chemotherapy/radiotherapy. Salving is merely a way of removing the tumour(s). It is still imperative that the whole health is addressed- both the internal body health and the psychological and spiritual health. As part of my own healing journey I have been doing lots of natural therapies (as mentioned in an earlier post), and will continue to do so, in fact much of the protocol is now just an everyday part of life. Black salve has been around for literally thousands of years. If you want to read further on the subject I would recommend a book called CANCER SALVES, A BOTANICAL APPROACH by Ingrid Naiman. Ingrid Naiman has extensively researched salves for many many years, her comprehensive book is the definitive guide to the use of cancer salves. She also has a very informative website, see  ‘Sacred Medicine Sanctuary’. http://www.cancersalves.com/pdf/CS-Introduction.pdf Another useful resource is http://www.blacksalveinfo.com A quick summary –

  • Black salve is applied to the area overlying the tumour. Apply an occlusive dressing to keep the salve moist.
  • The salve should be applied to the area every 12/24 hours for 1-4 days or until you start to see a good reaction developing.
  • After 1-4 days a reaction occurs on the skin if cancerous cells are present, i.e. yellow blister-like pustules begin to appear. This period can range from just a slight tingling/stinging sensation to extremely painful. If no cancerous tissue is present there will be just a slight reddening of the skin, but no accompanied blistering, and the reddening will subside after a few days.
  • The blistering reaction continues for several more days, as the active herbal ingredients work on necrosing the tumour.
  • A scab or ‘eschar’ starts to form.
  • The tumour becomes detached internally from the surrounding tissues, and the patient may experience a drawing/tugging feeling as the tumour is drawn to the surface. May also experience intermittent pricking/stabbing sensations. This stage is often described as more uncomfortable as opposed to painful.
  • The eschar and tumour come away when ready, usually onto the dressing, leaving a clean bloodless wound. The eschar should NOT be forcibly detached, it needs to come away freely in its own time. It is important that the wound shows no signs of remaining tumour (shown as residual white bits) – if so it may be necessary to reapply salve – which would be extremely painful to apply to an open wound. Alternatively, it may be an option to apply a less aggressive salve paste/yellow salve/drawing ointment/poultice, – this should be discussed with supervising practitioner.
  • The area should be cleaned daily with sterile (cooled boiled water), and covered with a sterile dressing until new skin starts to form on the area. Herbal healing creams with antibacterial properties may be used to reduce the risk of infection.
  • Anti-scar herbal creams may be used to minimise scar formation.
  • The whole process may take anywhere from 5 days to 5/6 weeks, depending on the depth of the tumour and the strength of the salve mixture.

So for my update… Whilst most people were busy during December planning for all the Christmas festivities, I have been busy otherwise – removing several breast tumours. Some of you may recall that my first black salve treatment was earlier this year, in August/September, where I removed a large breast tumour measuring 4cm x 3cm x1cm. This came out in 2 bits – the 1st bit after 21 days and the remaining larger part after 28 days. I took the large tumour to the hospital in a jar of vodka for histological examination, and I am happy to say that I have received histological confirmation that it was cancerous breast tissue – not that I didn’t think for one minute that it wasn’t, but I felt that it was important to have the confirmation on my medical records. Black Salve Day 20Black Salve Day 20 Tumour 1 This was part 1 that came out after 21 days. Some tumour was still remaining at the lower edge and at the side so I applied another salve application. The cream bit that resembles a piece of chewing gum is the tumour, the dark bit surrounding it is the black salve, and the brown stuff surrounding that is the poultice that I applied to help release the eschar. Photo showing a lovely clean, bloodless wound, with no signs of any remaining tumour 🙂 Black Salve Day 28Black Salve Day 28 Tumour 2 The wound has healed up beautifully, leaving just a small scar, with character might I add 🙂 The photo below was taken 8 weeks after the tumour was removed. 8 weeks healing 051114 I wanted to give myself a little time to get over the first salve treatment before starting on the second tumour. But then I received some not so good news in November, i.e. that the small tumour had grown from 0.9cm to1.4cm, and that there was also a tumour visible on the medial side of the breast measuring 0.9mm ( I was aware of a small lump in this area but I had been told previously by the surgeon that it was nothing to worry about, however on the most recent scan I was told it was likely to be cancerous). Anyhow, bearing in mind this news, rather than delay matters, I decided to get started with salving on the remaining two tumours. I began the 2nd salve treatment on the lateral side of my left breast on Friday 28th Nov and on Saturday 6th December out popped an irregular shaped tumour measuring approximately 1.4cm.This has been sent to pathology and I am currently awaiting the report. First photo was taken just after tumour came away. 2nd Salve Treatment Day 9 after poultice 6th Dec 20142nd Salve treatment Small tumour 6th Dec 2014 Photo below was taken 2 weeks after tumour removal. 2nd Salve treatment 2 weeks after tumour removal 13th Dec 2014

Then on 18th December I began a 3rd salve treatment on the medial side of my breast. With the 3rd treatment I applied the salve to the area where I could feel the small lump, and to my surprise a few days after applying the salve not only did a reaction occur in the area of the lump but also in a small area about 2cm lower down, even though initially no salve was applied to this area!  This indicated to me that a small 4th tumour was present, so on the next few days when I applied the salve I also extended the area of application to cover the lower part too.

The 3rd tumour came out in 2 pieces, the smaller bit (immediately to the left of the main crater) came out on Boxing Day morning, and the larger bit, about the size of a baked bean, came out on the evening of boxing day.

3rd salve 2nd day after tumours came out 28th Dec3rd Salve 1st bit 26th Dec20143rs salve 2nd bit 26th Dec evening

Then on the morning of 27th Dec the small bit lower down, measuring about 4mm came out.

 3rd salve 3rd bit 27th Dec am

There were also several ‘micro’ tumours – which on the photo of the wound area above you may be able to make out several small holes that look like acne scars – that’s where these came out from. Photo below shows the ‘micro’ tumours.

3rd salve 26th Dec micro tumours

This morning I called into the Breast Care Unit at St Luke’s Hospital, Bradford, and handed over my recent tumour haul to be sent to pathology. The breast care nurse, not surprisingly, seems very intrigued, and I am pleased to say she has been very supportive. She even gave me a supply of new dressings as I was running low. However, on my most recent visits to see the surgeon I have been at quite at a loss. He openly admitted he has never seen anything like it before, yet he appears to feign indifference. I may be wrong but I can’t help feeling that perhaps he finds me quite challenging , in a very unchallenging kind of way might I add. Afterall it goes against all he has been taught at medical school, and all his years as a specialist breast surgeon. I await to see how things develop over the coming months…

So moving on… I am hopeful that I  have now removed all the breast tumours, at least I am not aware that there are any more in there, and I’m hoping I don’t get any more ‘surprises’. I will be continuing to have regular ultrasound scans and thermal imaging scans to monitor my breasts for any signs of further disease. And as I mentioned earlier I will be continuing with my strict protocol for at least the next few years or until I am confident that I no longer have any signs of active disease, and even then much of my so called protocol is now in fact a new way of life for me. It is over a year since I was diagnosed and in spite of having the tumours I feel healthier and fitter than I have felt for many, many years. So it may come as no surprise that  I am happy to keep up my regime to reduce to risk of recurrence and to maintain my new found health.

So, here’s to finishing off 2014 with a bang,  I’ve had quite an eventful year…

  • Regan and I started the year off as newly weds 🙂
  • I have avoided having a mastectomy 🙂
  • I have avoided chemotherapy and radiotherapy, along with the accompanying side effects 🙂
  • I have successfully removed 4 breast tumours, non-surgically! 😉
  • Had a lovely holiday in Spain 🙂
  • Had a great long weekend in Finland, with  my new husband, two sons, and the European Round Table.
  • I’ve sent my eldest son off to University 😦
  • My youngest son continues to be a daily delight 🙂
  • I have completed a full year’s Focussed Mindfulness Programme, and am working towards practitioner status 🙂
  • I organised and ran a Cancer Prevention seminar in June in Brighouse, about 70 people attended and we had fantastic feedback 🙂 Thanks to my old boss Art and his lovely wife Rosemary for coming up all the way from the south coast.
  • Along with the fabulous Nina Joy (www.ninajoy.com)  –  ‘Whaddya mean Incurable? –  and the inspirational Clare Walters we have set up ‘The Cancer Mavericks’  – a support group to help people with cancer – to help make them aware that they can take an active role in overcoming the disease and getting back to full health. More to follow…
  • The Cancer Mavericks ran a very informative one day seminar, focussing on Cancer prevention, in Wakefield in October. About 80 delegates attended, with fantastic feedback.
  • The Cancer Mavericks are planning a one day workshop, specifically for people with cancer, on 7th Feb 2015. See Cancer Mavericks FB page for info.
  • I had the privilege of meeting Chris Woollams of http://www.canceractive.com
  • I’ve been to two great YestoiLife seminars http://www.yestolife.org.uk.
  • I have been made aware of an amazing therapy called Bioresonance, which has been an important part of my get well programme. I have been so impressed that I have invested in a BICOM Bioresonance Machine, and will be getting started with training in January 2015 and May 2015. More to follow, in the meantime if you would like to know more see http://www.reson8uk,com
  • It was with sadness that my Aunty Margaret Devlin recently died, I hope she is resting peacefully and is now with her two eldest children, Ann & Bernard, – my two cousins who both died of cancer at the age of 40 and 41 respectively. Though it was a sad occasion, it was also a lovely opportunity to meet up with many family members who I have not seen for many years.
  • Regan and I have got through our first year of married bliss – I’m happy to say that he has been unbelievably supportive and when I have been faced with many difficult situations and decisions he has been beside me all the way.
  • I have had a wonderful peaceful Christmas, albeit I was a bit sore, and I look forward to many more Cancer Free Christmasses 🙂
  • I have met some absolutely wonderful new friends over the last year, both in person and online, many of whom I hope will remain long term friends. Thank you so much for your support and friendship 🙂
  • Thanks also to the many family members and old friends who have been there for me too, and the school mums 🙂
  • Finally thanks to my Utility Warehouse buddies and my Utility Warehouse business  – the residual income has allowed me to step back from the business and instead has allowed me to focus on my health, and my UW business is still secure and growing.

So to finish I’d like to wish you all the best for 2015, with lots of Love, Peace, Happiness, and Health! Hygge Annx

29th December 2014 – Update on my Cancer journey

Geopathic Stress and Chronic Illness

IMPORTANT: – ANYONE WHO HAS CANCER, OR HAS HAD CANCER, OR WOULD LIKE TO REDUCE THEIR CHANCES OF DEVELOPING CANCER, OR OTHER SERIOUS CHRONIC ILLNESSES…. you need to know about geopathic stress.
Most people would agree that there are many factors that contribute to developing cancer. Doctors are now accepting that diet and lifestyle play a major part. This is great progress, and means that people can take steps to improve their health. However, sadly there’s another massive contributory factor that gets very little attention, and most people brush it off as insignificant – ‘cos we can’t see it and can’t see the damage!! And because it’s not in the interests of ‘big business’ and governments for this to be in the mainstream media… It also explains why many otherwise ‘healthy’ people develop cancer and other serious illnesses. I seriously believe that in all cases of cancer and other serious illnesses such as ME, that radiation stress is a contributory factor. This documentary goes a long way to explaining how serious this is, and it is something that’s been known about for many, many years! I used to be a radiographer – the dangers of radiation were hammered into us, yet why are people not taking other types of harmful radiation seriously? Please take the time to watch this documentary, please show it to your children/grandchildren. We can’t rely on governments to protect us, we need to educate ourselves and do what we can to protect ourselves… Bioresonance can help as far as detecting geopathic stress, and can help to alleviate the negative effects on the body, but it is also really important to prevent further stress – you can use mobile phone/tablet protection eg. WaveWall and Radisafe, switch wifi off when not in use, switch mobiles off/flight mode at night and do not keep them close to sleeping area, old fashioned phones are safer than modern DECT phones, avoid (not so) smart meters, use crystals to counteract negative radiation, an especially good crystal is Smokey Quartz. Get your home/workplace checked for radiation stress – checkout Geo-safe – E – trained practitioners who can check your home/sleeping place and can make corrections.

A fascinating documentary…

Other useful resources…

http://www.positiveenergy.ie

more info on natural/earth radiation https://swissharmony.com/earth-rays/what-is-the-curry-grid/

http://www.baubiologie-schaefer.de/index.php?id=dasprinzip&L=1

A free book that you can download covering plenty of information on natural and man-made sources of EMF
http://www.emf-safety.com/uploads/1/0/2/0/10206075/radiation_fields_ebook_emf-safety.pdf

Also see:
http://www.rolfgordon.co.uk
‘Are you Sleeping in a Safe Place? by Rolf Gordon

And another very interesting book:
‘PEMF The 5th Element of Health’ by Bryant A Meyers

‘Geopathic Stress and Subtle Energy’ by Jane Thurnell-Read

WHO classifies mobile phones as a CLASS 2B carcinogen –
‘possibly carcinogenic to humans’
http://www.iarc.fr/en/media-centre/pr/2011/pdfs/pr208_E.pdf

http://www.radisafe.info

http://www.groundology.co.uk

Geopathic Stress and Chronic Illness

A well overdue blog update, a farewell to 2016, and a welcoming in the New Year!

Hi All, this is somewhat of a well overdue blog update. I am regularly still asked about my cancer experience and in particular the salving of the breast tumours. I’d like to clear up any confusion. If you are interested in knowing more about what I was up to as far as my cancer therapies you can check out some earlier blog posts, but for the purpose of this post I wanted to concentrate on the salving, the surgery and the final outcome.
I was diagnosed with multi-focal breast cancer on 2nd Dec 2013. The mammography picked up one large tumour about the size of a golf ball, and a second smaller tumour at the lateral side, measuring about 1.4 cm. It turned out later that the mammography had missed several smaller tumours and I did in fact have at least 4 small tumours ranging from ranging from 0.5cm to about 1.4cm, plus lots of tiny ‘microtumours’. In total I salved about 7-8 times. I managed to successfully remove the smaller tumours, that were more superficial, as well as an immeasurable number if microtumours. However despite salving the large tumour repeatedly about 4-5 times I could not get to the deeper stubborn part of the tumour and I became very drained, both physically and emotionally, from doing the repeated salving (deep salving is not exactly a walk in the park!). After much thought and deliberation, and also a very fortuitous chance consultation with the fabulous Caroline Myss, I decided to have the surgery after all. It is now just over a year ago since I had the surgery, 3rd Dec 2015, and 2 years after my initial diagnosis (2nd Dec 2013). I had a skin sparing nipple sparing mastectomy with implant, covered with SIS biomaterial, made by the Cook Medical – the company I used to work for! The biomaterial covers the implant to prevent erosion of the implant through the skin, which can be a problem with implants that are placed for breast cancer surgery as there is no breast tissue between the implant and the skin. Traditionally the surgeons overcome this by removing a flap of tissue from the back muscle, turning it around on a pedicle in the armpit area, then placing it over the implant – this is quite extensive surgery, and not without significant complications. The option I went for is a new procedure which has only been practiced over the last few years since the introduction of suitable biomaterials. The surgeon I am under, Mr Rick Linforth at Bradford Teaching Hospitals, was the first surgeon in the UK to perform this type of reconstructive breast surgery, and has subsequently taught several more surgeons.(The implant erosion is not an issue when implants are placed for breast augmentation as the implant is placed in a pocket beneath the breast tissue). I found it quite amusing that when I was working with Cook I had been heavily involved in the early use of SIS mesh, for veterinary use, well before it was approved for human use! Then many years later I came to rely on the same mesh for my own surgical intervention. This SIS mesh is truly magical stuff, – it is gradually absorbed and remodeled by the body and eventually becomes revascularized and takes the form of existing flesh. When I was with Cook I was involved in working with vets who were using the product on dogs who had serious degloving injuries (where huge chunks of muscle and tissue were missing due to car accidents – it was totally amazing to see first hand how effective it was – the whole tissue would gradually regenerate, and even grow new skin and hair. In the 1990’s Cook SIS even featured on ‘Tomorrow’s World’ – for any of you that may remember that great program. It then started being used in humans initially for hernia repairs, and bladder suspension surgery, and in time has now become used for many many other surgical procedures. The biomaterial is derived from pigs intestines so may not be suitable for all. For more info see: https://www.cookbiotech.com/technology/

Anyway,the op went really well, the surgeon was great, very patient and understanding, unlike many others I hear of, and I healed very quickly. I have thankfully been cancer clear since then. Although in my case I still ended up having surgery I know of several others who have managed to deal with breast tumours without surgery. I am still a big advocate of salving but I feel that my case shows that there is still a case for surgery too. In fact from the beginning I was always open to the option of surgery and my forays into natural cancer treatments were primarily to avoid chemo and radiotherapy, as to me they instinctively felt so wrong at that time. As it was two years following my diagnosis when I eventually had surgery I feel all the ‘natural’ stuff I had been doing had strengthened my body and my immune system, and had prevented the cancer from spreading, but stilI I was not quite ready to let go of my big tumour until I had the surgery. The mind works in mysterious ways – I often wonder if it was because deep down I had been open to surgery then that’s what I still needed to do. I am still happy to support other people who feel they would like to salve, in many cases it may still mean being able to avoid surgery. Though I feel it is a matter of weighing up the options and reaching a balance as far as how much salving one is prepared to do. One must bear in mind that salving is a not a cancer treatment, it is merely a way of removing the tumour mass, and still lots more needs to be done to correct the internal body environment and also the emotional blocks and traumas that may have caused the cancer to develop. Also, as with surgery – many times a surgeon may do a lumpectomy but unfortunately when the histology report comes back from the lab it may state that they have not got ‘clear margins’ i.e. they like to have at least a full centimetre of healthy tissue surrounding the cancerous tissue to be sure there is absolutely no remaining tumour left, otherwise it may subsequently be given a chance to re-establish itself. So, when the lab report say unclear margins it tends to mean a second op is necessary and that usually means a mastectomy. You could say that this is in a way what happened in my own case – I did several of my own DIY lumpectomies but couldn’t quite get the clear margins on the large tumour, so in the end I still required the assistance of my surgeon for the mastectomy. On another note I am so glad that I did not rush into having the mastectomy at the time I was diagnosed, even though I felt under so much pressure to do so. If I had I am convinced that it would not have been a good outcome. I believe my body and immune system at that time was in such a weakened state that had I had surgery as recommended I would not have healed well and I feel it would have been inevitable that I would have developed secondary tumours. I will be forever grateful to a anaesthetist friend, Dr Andrew Bodenham, of mine who advised me to not rush into making any decisions, he advised me to take my time, ask for a second, third, or even fourth opinion if I did not feel at ease with my medical team. This was profound advice at the time and so contrary to the usual cancer rush rush rush scenario. When someone is diagnosed it’s more than likely that the tumour has been quietly growing for many years, and a few more weeks or even months in delaying the start of treatment is unlikely to alter the outcome in a negative way. On the contrary I feel by pressing the pause button and using this precious time to detoxify and build up the body, and also to research and reflect what feels right for each individuals cancer treatment, rather than blindly stepping onto the NHS cancer conveyor belt and later finding unable to make any decisions but just being railroaded that this time for reflection and regeneration could be absolutely crucial as far as far improving the outcome. And I feel that would apply across the board, in fact more so to those who are opting to undergo the conventional cancer treatments. If people are going to be subjected to major surgery, followed very soon after by debilitating radiotherapy and toxic chemo, doesn’t it make sense to build up their strength beforehand so they stand a much better chance of holding up against the harsh treatments. If you were sending men into battle wouldn’t you prefer to have 300 well fed Spartan warriors, rather than a 300 sick undernourished waifs? Which would stand a better chance of survival? ( perhaps not the best analogy since the Spartans get defeated – but hopefully you get my point, and they were up against 1000’s!) Also it’s worth mentioning that it’s often said amongst oncologists that the aim of the harsh cancer treatments is to kill the cancer before it kills the patient! So you think they’d get it too that it make sense to build up their patients and prepare them, both physically and emotionally, for what is likely to be the most important battle of their lives.
The last three years, since being diagnosed, has been a very interesting time for me, I have learnt a lot and radically changed my so called ‘lifepath’ as a result of my cancer experience. I feel I am now totally awake as to the injustices in this world, at all levels, usually fueled by selfless greed and money by big corporations and corrupt governments. At the same time I have been so heartened by the immense goodness in the world too, though it may not always be so obvious as the corrupt media bombards us on a daily basis with nothing short of propaganda to try to keep us submissive. It’s thanks to many caring individuals, including the many holistic doctors and practitioners who are willing to speak out against the powers of Big Pharma and the massive greed and corruption that controls our societies, and instead try to open people up to other possibilities. If you are not already aware the count is now up to about 80 holistic doctors, including the wonderful Dr Gonzalez from New York, and Dr Bradstreet, that have died in suspicious circumstances over the last 18 months…and this doesn’t get any media coverage!
http://www.healthnutnews.com/recap-on-my-unintended-series-the-holistic-doctor-deaths/

Finally, just to say I am healthy, cancer free, and looking forward to a great 2017. I would like to wish you all a great 2017, with lots of health and happiness, and especially to all my buddies who are still struggling with cancer, and anyone else for that matter, I sincerely hope and pray that you can get onto the right healing wagon and get it licked soon!,
Ann
Hygge

A well overdue blog update, a farewell to 2016, and a welcoming in the New Year!

Cannabidiol Cancer Research

If anyone would like to help as far as cancer research then rather than keep giving money to the big charities so they can develop more drugs that don’t work, or at least not particularly well, and who in turn line their own pockets and their shareholders with their vast profits, then why not donate a few squid to help fund research into the use of cannabis to treat cancer? There is already lots of anecdotal evidence and plenty of in vitro (lab) evidence to support the use of cannabis as an effective cancer treatment but more research is needed to identify the best types of cannabis strains/compounds,and how different types of cancer react. PLEASE DONATE AND PLEASE SHARE

http://www.gofundme.com/CancerCannabinoids

See this fantastic video about how the lovely Shelley cured her so called ‘terminal’ lung cancer using cannabis…https://www.youtube.com/watch?v=-hUoyXKf81c

Cannabidiol Cancer Research

A Sobering Statistic

Most people would be shocked to discover that approximately a third of early stage breast cancer patients go on to develop stage 4 metastatic breast cancer, which according to the medics is incurable, or at best has a survival rate of 2-3%. It amazes me that many people seem to trivialize early stage breast cancer, saying ‘Oh well they caught it early, you’ll be fine’ etc, etc, but are they aware that it still means that with early stage breast cancer the woman has a 1 in 3 chance of dying from it! I was not told this statistic, I found it out for myself . Should women be made more aware of this statistic so they can take on more measures themselves to fight the disease, i.e. through diet/lifestyle changes, and complimentary therapies, rather than just rely on conventional treatments? Unfortunately in many cases it’s not until a woman is re-diagnosed with metastatic breast cancer that they start to take control and implement lifestyle changes, but often it is too late. Thanks so much to Holley Kitchen for making this video, it is a great way to raise awareness. From it I’d personally like to see that women would put in place more measures as far as prevention, and if they are unfortunate enough to be diagnosed then they should do all they can within their own power to take control of their own health and not just rely on the doctors.

As many of you know I opted not to have conventional treatments to deal with my own breast cancer. I realise the numbers would be far too small to have any statistical significance, but I feel it would be interesting to know what the statistics would be for women diagnosed with early breast stage cancer who choose to avoid chemotherapy and radiotherapy, and instead use natural/non-toxic treatment methods. It is well established that chemotherapy and radiotherapy themselves are known to cause cancer, as well as chemotherapy destroying the immune system at a time when the patient needs it the most. It would be my feeling, and I’d love to see it proven someday, that recurrence and indeed re-diagnosis as stage 4 metastatic breast cancer would be less if breast cancer was treated routinely in a non-aggressive manner.

Another interesting statistic that many people may not be aware of: 2 recent studies have shown that chemotherapy is only 2.1% and 2.3% effective. If people were told this information I wonder how many more people might reject chemotherapy in favour of natural/non-toxic treatments.

A great book that covers many, but not all, of the most successful and widely used non-toxic treatments is ‘Outsmart Your Cancer’ by Tanya Harter Pierce. A book that anyone who is diagnosed with cancer should read as a priority, or even if you don’t have cancer it would be good to read, after all ‘To be forewarned is to be forearmed’.

A great website for information on cancer prevention is http://www.canceractive.com

A fabulous little book that I would recommend every woman should read is ‘The Oestrogen Factor’ by Chris Woollams (available from the Canceractive website).

Please take the time to watch Holley Kitchen’s sobering video: https://www.youtube.com/watch?v=QDQ0FjP7J-c

Apologies for the not so cheerful post, but, same as Holley, I feel it is really important to raise awareness.

I’d like to finish on a more positive note. I often feel very angry and frustrated that the doctors dish out the ‘terminal’ diagnosis to their patients without really thinking about the impact on the patient. Afterall, if the doctor tells the patient they are going to die, it’s more than likely that they will believe it, and so the patient may reside themselves to the fact that they are going to die, and it inevitably becomes a self-fulfilling prophecy. I realise the doctors are limited to the treatments they can offer, and the majority are just going by what they have learnt in medical school, but they would do well to read up on the thousands of so called ‘spontaneous’ remissions. When one looks into these cases in more detail they are far from spontaneous. It appears that some people who receive a terminal diagnosis are unwilling to accept it, so they pull out all the stops to make sure they recover as they are just not ready to accept the diagnosis and give in. I would highly recommend anyone with cancer, or any other serious disease, for that matter to read a fantastic book called ‘Radical Remissions’ by Dr Kelly Tumer PhD. Kelly Turner has spent 10 years researching this fascinating ‘phenomenon’. She has interviewed more than a 1000 people who have recovered from cancer against the odds, most of them being Stage 4 and for whom conventional treatments had failed, yet they still went on to make a full recovery! Dr Lissa Rankin’s, another very progressive doctor, highly endorses Kelly Turner’s work. See link below for review of the Dr Kelly Turner’s book.

http://lissarankin.com/9-key-factors-affecting-radical-remission-from-cancer

See also THE SPONTANEOUS REMISSION PROJECT – A study of 3500 ‘spontaneous’ remissions. It’s not as rare as most people would think…

http://noetic.org/research/projects/spontaneous-remission

And just remember….

It ain’t over till the fat lady sings!

A Sobering Statistic

A Remarkable Place

Hi Folks,

I’m just back from having spent a wonderful three days at the Penny Brohn Cancer Centre, formerly known as the Bristol Cancer Centre. This was my second visit, and I feel words can’t express enough my gratitude to the facilitators, the therapists, their resident doctor, the catering staff, other support staff, and of course to the many people who have contributed funds to keep this most wonderful place running. And must not to forget a special mention for the beautilful Elizabeth – Biodanza dance instructor and truly wonderful woman, and the gorgeous Tilly – the ‘Night Nurse’.

Personally I feel every town and city should have a Penny Brohn Centre, but that may be a very long term vision indeed. I feel the benefits it offers to cancer patients, and their carers too, is beyond measure.

If you or any of your loved ones have cancer I would highly recommend you check out their services.

If you feel the urge to donate please do so as they are certainly a charity in need of support so they can offer support to the growing numbers of people being diagnosed with cancer every day.

Penny Brohn herself, and the co founder Pat Pilkington were both truly inspirational women with a vision to help cancer sufferers by implementing a whole person approach, which is unfortunately sadly lacking in the conventional cancer treatment model. It is slowly becoming accepted in Western society that stress, emotional/psychological problems, and nutrition play a significant part in the development of cancer, and it is essential that these aspects are addressed if the person is to recover, to be able to manage the disease, and to reduce the likelihood of recurrence.

Please take some time to look into the background of The Penny Brohn Centre and the services they offer, even if you don’t need them now – you might be glad you did as you or someone you know may have need for their services in the future.

http://www.independent.co.uk/arts-entertainment/obituary-penny-brohn-1070229.html

http://www.pennybrohncancercare.org/

Thanks again to all the staff and supporters of Penny Brohn centre, and thanks to the amazing group of people that I met there, both this week and on my first visit last December.

Hugs,

Ann X

A Remarkable Place

An Inspiring Evening

Last night I had the pleasure of meeting a wonderful couple Sue and Robert Olifent.

They have been on an amazing cancer journey.

Robert’s wife, Sue, was diagnosed with ‘terminal’ cancer, she had a large liver tumour plus several smaller tumours in her pancreas. The doctors gave her no hope whatsoever, in fact the doctor gave Robert a plentiful supply of painkillers and sleeping tablets, and his parting words were ‘She’ll need these’.

Fortunately Robert  and Sue took control of a desperate situation and implemented a great programme of nutrition, detoxification and supplements. Sue made a full recovery, and has been cancer free for 4 years.

Sue and Robert now devote their life to helping other people with cancer. Robert has written a very informative book, a great resource.

http://cancer-acts.com/

Big thanks to Sue and Robert!

An Inspiring Evening