Causes, prevention and humane, up-to-date treatment Real-life research by Al Smith and Faith Warn
Latest News, updates, comments together with latest entries from Al's blog Scroll down for earlier news items
Al's heroic journey 5th September 2007 by Faith Warn
Al Smith, who created this site, died of metastatic prostate cancer on 31st May 2007. His death was neither defeat nor failure but the end of his soul’s journey – and what a journey! Al was always a beautiful, creative, unassuming person with quiet strength. In the last two and a half years of his life, he truly seized his own power and moved mountains. His achievements and courage have inspired people around the world and are helping to change the way prostate cancer is treated. Al’s last blog reports that, in response to the cancer spreading to his bones and causing pain, he started a course of Zoladex hormone treatment. It was intended to reduce his PSA and symptoms, as it has in so many other men. This would be only until new alternative strategies had time to take effect – again, as they have done successfully in other men. (Al was mainly using a natural substance that deprives cancer cells of blood supply combined with heat treatment, which kills them off. For details, please contact Yes to Life.)
But instead of falling, Al’s PSA rose frighteningly fast, the pain worsened, his movement was restricted and he became very unwell. We struggled with his GP to get consistent support and effective pain relief and finally he was admitted to hospital by his oncologist. There, he received some radiation treatment on his spine, but the cancer had already taken too strong a hold. He was transferred to the Pilgrim’s Hospice near our home in Ashford, where, his hand in mine, he slipped away gently on a calm, sun-filled evening.
Throughout this time, in spite of the pain, Al seemed serene, at peace with himself and full of love. Ever since his diagnosis, we had worked together to find a humane and effective solution, and for him to take control of his illness and destiny. In the last few months, he seemed to truly find his power – and then it was as though he’d had enough. He asked us not to be sad; his soul was ready to move on to a new adventure.
This website was an important part of Al’s expression of strength. However rocky his path, he was determined to share it with other PCa men and their families, to encourage them to find power and hopefully to heal. He was also determined to challenge the medical profession, both conventional and alternative, to address themselves urgently to making better treatments accessible to all. His life – and death - has touched both hearts and minds and the impact of that will grow.
It’s more than five months already. Five months spent settling back into life in England after 11 years under the blue skies of Kalymnos, that Dodecanese isle splashed by the equally blue seas of the Aegean. Surprisingly, the weather has not been a major problem. A kind winter, softened even more by good central heating and a log burning stove, and a beautiful springtime capped by a dazzling Easter weekend has eased the transition.The village is peaceful and friendly with ‘good morning’ greetings exchanged freely on the street and in the local store/post office.If it wasn’t for the cost of living, with exorbitant council taxes and utility charges, I could borrow a phrase from Pop Larkin in The Darling Buds of May and say ‘Just perfik.’
The prostate, however, has not been playing ball. My trip to Lisbon did not bear fruit and with a PSA having risen to 178 needing firefighting a strategic - and hopefully short-term - course of hormone therapy was started four weeks ago with Casodex and then a Zoladex one month implant. This should get the numbers down to a manageable level and give breathing space while various new alternative treatments come into play. In the meantime a CT and then a bone scan have given a closer look at what is really happening inside.
I’ve just seen the oncologist and she reported that the PSA had ‘plateaued’ in the short time since re-commencing the hormone therapy. Also that the CT scan had indicated several sclerotic areas in both iliac wings and probably two lumbar vertebrae suggestive of bony metastases.
The bone scan has been reviewed and it was concluded that there is a very small tumour in the lower spine and small metastases in the iliac wings - too small for hot spot radiotherapy ‘zapping.’ A course of bisphosphonates taken intravenously was proposed to strengthen the bone and I am researching this to decide shortly whether to take this route. A Strontium mineral supplement is also being considered as an alternative.
Physically, I have been suffering back pain on and off since January, when a long established wedge fracture was revealed by x-ray. Since this pain is NOT in the areas of suspicion indicated by the scans, it does seem that it is emanating from this fracture and associated spinal ‘wear and tear’ and I have been swallowing analgesics to cope with it.
The doctor at the local pain clinic suggested giving acupuncture a try and taking the painkillers as a suppository and/or a transdermal patch to lessen the risk of gastric damage from prolonged pill taking. I have my first appointment with the acupuncturist this afternoon.
To finish, I must thank Yes to Life, Cancer Options and the Really Healthy Co for the invaluable help and support that I have received through this period of difficult decision making.
Yes to Life fundraiser, 25th January 2007, London 11th January 2007
The charity Yes to Life helps people with cancer form a personal strategy based on real choice - including non-toxic complementary or alternative treatments. For those in need, funds are available for consultations and treatments not generally given through the NHS. Recognising the pressure and hardship of cancer, Y2L also helps patients access all possible resources for support. Yes to Life was set up by Robin and Nancy Daly after the loss of their daughter, Bryony. The couple's powerhouse of energy and dedication has quickly advanced their cause and Robin has worked with us to spread information and research about effective, up-to-date treatments for prostate cancer, including the Pfeifer protocol. On Thursday 25th January, Y2L will hold its first major fundraiser - a dinner, dance and auction at the Wallace Collection, London W1. We'll be there and expect it to be lots of fun in a very worthwhile cause. Tickets at £180 each from 0207 317 3459 or email Robin at yestolife.org.uk.
Pfeifer to talk in London 10th October 2006
Prof Ben Pfeifer is taking time out from his busy schedule at the Aeskulap Cancer Clinic in Switzerland to talk in London this Sunday, 15th October. At Camexpo, the complementary & natural healthcare show held at Docklands' Excel Centre, he will update an eager audience about his work with prostate cancer and reveal new research into natural breast cancer therapies. It was at this event in October 2005 that Prof Pfeifer launched his phytotherapy protocol in the UK. Shortly afterwards, we read the text of his talk online and resolved to try this treatment for Al. For Faith, Sunday is a red letter day as she will meet the Professor for the first time. Look out for her report next week!
We have been in UK just over a week and it's update time. My part in the 6 month study at St Barts London hospital of the phytotherapy protocol of herbal treatment for prostate cancer has come to an end with encouraging results. My PSA has settled back to a reasonably low level while my urine flow continues to be full with none of those 'must go' episodes. Other indicators such as white blood cell levels and haemoglobin are strong. I am continuing with the treatment and feeling positive about the future. Our website at www.prostatecancernow.org is gathering momentum and Faith is filling her diary with meetings to persuade other consultants and hospitals to initiate similar tests to the one that I have been involved in. A national newspaper is also on the scene but we are holding fire on another interview until we have something even more exciting to announce than a re-run of the earlier Daily Telegraph article.
New FAQ's 18th August 2006
The full text - and even video - of Dr Pfeifer's presentation explaining his protocol to a London audience of experts and non-experts has for some time been available online It makes fascinating reading - and the video shows clearly the humanity, compassion and awesome expertise of this remarkable cancer specialist. Now, this really useful site has added a new page of FAQs. It gives full answers about the protocol and how to use it, how to contact Professor Oliver and the option to book a phone consultation with Dr Pfeifer himself to get individual advice based on your unique case history and needs.
Blood Tests - Greek style 3rd August 2006 - blog entry
Kalymnos is awash with all shades of medical advice. Signs for walk-in dentists, radiologists, dermatologists, GPs and gynaologists pepper the high street and many side streets. You may have read of my experience with the local urologist (if you haven't, click here and go to 24th November 2004). Now I’ll tell you about blood tests - Greek style. An essential part of my treatment study is a monthly report to Prof Oliver back in St Barts, London. This includes general blood tests plus any movement in PSA and testosterone. The NHS in UK has a reciprocal arrangement with Greece’s IKA. My IKA doctor holds a busy surgery every weekday morning. It mainly deals with repeat prescriptions for the locals and I try to be there by 8.30 to be near the front of the queue when Dr Peter arrives about 9am. Luckily for me he is American/Kalymnian so speaks English. He is quite thrilled to be involved in my treatment study with an important consultant in London. He writes me two scripts to take to two separate mikrobiologists - one for the routine tests and another for the PSA/testosterone. Seems straightforward? No problem? Umm, we now have to factor in Greek bureaucracy. IKA prescriptions for specialist involvement require scrutiny, counter-signing and rubber-stamping by a senior medico. Ours is a gynaecologist so I share his waiting room with Kalymnian ladies at varying stages of ripeness. It's my turn and I enter the inner sanctum where a wall is dominated by a huge portrait of the man himself. I immediately think of Dorian Gray - in reverse. It depicts him about 25 years younger but with the exact same comb-over (black instead of grey), steel-rimmed spectacles and humourless gaze. Weird, or what? He compares me carefully with the photo in my IKA book and begins flourishing signatures. His hand freezes over the handle of the crucial rubber stamp. Oops - a problem! Apparently, PSA tests are expensive and rationed to be performed on the first of each month; my requirements are for tests to be taken mid-month. To get around this Dr Peter writes ‘emergency’ - in Greek of course - on the prescription. I then pay for the test and claim a refund from IKA. But this time Dr Peter has forgotten the essential endorsement. Stalemate. A fleeting gleam behind the specs hints at some rivalry with my friendly GP. “PSA first of month only”. I stand my ground, implying that upsetting an important consultant at a leading London hospital could puncture his reputation. He crumples and approves the ticket so long as I get it endorsed before claiming my refund. The most important, redeeming point to all this is that the results of any of these tests are MY property, with none of that frustrating waiting until my doctor receives them days later and then maybe deigns to make broad, filtered statements without allowing sight of the actual results. I collect the printouts from the lab, show them to the GP for comment and take them home.
Prostate still being contained 21st July 2006 - blog entry
Monthly general bood test time has come around again, showing little significant change over last month. PSA has moved up slightly, but is still below 10. Nothing to panic about and Dr Pfeifer has suggested an adjustment to the protocol dosages to counter this trend Our new website, prostatecancernow , has been up and running for a couple of weeks with very encouraging feedback. Check it out if you or someone you know has concerns with the prostate. Everything you wanted to know but were afraid to ask
News item 7th July 2006
In 2002, David Hillier, chief economist at Barclays Capital, was diagnosed with advanced prostate cancer at the age of just 37. On Monday, he will cycle in a gruelling stage of this year's Tour de France, feeling fit and enjoying a very low PSA. At diagnosis, doctors in London told David they would treat him with androgen ablation and gave him two years or less to live. Appalled, he took power and found an enlightened oncologist in New York, who used chemotherapy and radiation to debulk the tumour and then advised David that exercise would give him a better chance of fighting the cancer. The exciting significance of this strategy is that vigorous exercise like cycling raises testosterone to normal or high male levels - and that's precisely the way some other men have fought prostate cancer and remained well for years. We hope to reveal more about the details of David's case soon. Meanwhile, this inspiring man is using the publicity and funds from his Tour de Force to raise awareness and help for men and their families through the Prostate Cancer Organisation. What a great chance to get behind research and promotion of the strategy David is pursuing! Check out David's story here
Want a talk or lecture? 5th July 2006
Faith is taking bookings for talks and lectures in 2007