Winter update

It’s been an interesting past few months with my oncology treatment. The very personable consultant (!!) has decided I can resume chemotherapy, if somewhat grudgingly, although she would really have liked me to take a chemo break. Many other oncologists are savvy enough to admit that pancreatic tumours just love a holiday. Gives their malignant cells a new lease of life! So, I’m not going to be signing up for a holiday, not just yet. But before restarting chemo, I am scheduled to have repeat scans.

In the interim a new battery of cancer tests are being developed by Glasgow Precision Oncology Laboratory, called Glasgow Cancer Tests. These are a suite of affordable tumour and blood tests designed to be used routinely. Looking at a sample of a patient cancer to screen for biological markers, they aim to allow every cancer patient access to the latest in treatments and clinical trials.

Presently these are being evaluated by NHS labs in England and Scotland, and in addition are being used in a University of Glasgow led Precision-Panc clinical trial for pancreatic patients.

I was pleasantly surprised to read of a new potential treatment for our fellow pancreatic sufferers. This new discovery by researchers at Sheba Medical Centre, Israel, found that pancreatic cells were almost completely eradicated in 2 weeks by using a drug known as PJ34. By the way, is my oncologist reading this??

Recent news scathingly states that breakthroughs in cancer drugs – which could drastically extend lives – can take decades to reach patients in the NHS. This has been evidenced through a study by the Institute of Cancer Research, who found that between 2009 to 2016 it took an average of 14 years for treatments to become available on the NHS. It took 22 years for a drug called trabectedin, used in soft tissue carcinoma, to go from being patented to getting the final go-ahead from NICE, our British regulatory body. The problem is that these breakthrough lifesaving drugs have to not only pass relevant clinical trials and then be authorised, but they then have to be approved as cost-effective and that puts a massive burden on the manufacturers because they may be curative but not cost-effective. By the time they have gone through the red tape, many more people will have died. Another drug created to treat bone cancer took 20 years to reach NICE approval, whilst the breast cancer drug olaparib, which got the go-ahead from the FDA in the States more than 2 years ago, still has to be approved by NHS watchdogs.
Whilst on the dreaded topic I expect most people will have realised by now I take this cancer very VERY seriously. I intend to beat it, if it can ever be beaten. My view is that something has gone wrong organically with misidentification of rogue cells, but that there must be – conversely – a way to reprogramme those same cells to be identified as invaders, as parasitic, and destroyed accordingly.

Conventional chemotherapy is systemic, in that it targets something but attacks everything within its path to catch the ‘bad guys,’ but often it is like zapping a wasp with an atom bomb. (okay, I exaggerate, but you do see my point) I wanted to flag up that there is a new organic product that I am trying, sent to me from the United States, but is not available here.

It is currently being ‘put through its paces’ by the FDA, as a tumour killer, sometimes destroying tumours within a matter of months. I’ve read the research papers and have been trying this particular product for only a few weeks. Having been on a merry-go-round of scans during the past month, my latest results are showing a previously unseen (til now) reduction in tumor activity. The oncologist was baffled by this apparent progress, and their report remarked that I ‘seem to be responding to treatment.’ Well, if anything, I think it might be a combination of conventional and alternative methods. But there remains the possibility that the change could be credited to the maverick product.

I was very honoured in early December to attend a reception for the community, to meet HRH The Prince of Wales at Buckingham Palace. It was a splendid affair, with many dignitaries in attendance, including Lord Winston, Lord Pickles, Chief Rabbi Mirvis, Simon Sebag Motefiore, celebrities and many, many normal people from all walks of life. I met representatives from charities such as Camp Simcha, Norwood, Chai Cancer Care to name only a few.
HRH Prince Charles spoke eloquently as ever, mentioning the positive impact our community has on the world at large, that we often triumph in adversity and was particularly touched by the fact we – as a community – pray for the continued welfare of the Royal Family every week.

There were, of course, some light hearted moments, one being when he mentioned his beloved paternal grandmother Princess Alice (one of the Righteous among the Nations). She insisted on being buried on the Mount of Olives, but when family members questioned ‘how on earth they would get there’, she replied indignantly .. “it’s only a bus ride away!” Small groups of delegates got to meet the Prince individually, and during our few moments of conversation, I told him I was giving a charity fundraiser and he was touched I was doing it in my capacity as a cancer sufferer also.


I told him I was giving a charity fundraiser and he was touched I was doing it in my capacity as a cancer sufferer also.
This year my concert was in aid of Motor Neurone Disease and Oncology.

We raised a total of around £7,000 which should make a welcome contribution to charity funds. Thanks so much to all who attended or made a donation.

Back soon x