I am incandescent at the latest Daily Mail article: “Does breast cancer screening do more harm than good?” with opposing opinions from a Professor of Surgery (yes) and a Consultant Radiologist (no).
My cancer was found on my 3rd, 3 yrly breast screening, when I was 58 yrs. I had no symptoms whatsoever and on receiving the recall letter I had to see my GP about another problem and asked her to feel both breasts as I couldn’t detect a lump, no matter how small - neither could she.
To say I was shocked on seeing the original mammo is an understatement. There was a big, black spiculated mass on the x-ray and I knew, absolutely, it was cancer, although I knew nothing about bc. The tumour was non palpable.
I do wonder now, if annual screening was available, whether my cancer may have been picked up before it had spread to my lymph nodes. My friends in the US, as a condition of their medical insurance, must have an annual mammo and are shocked that we only get 3 yrly mammos, and then after 50. They start having mammos at 40 yrs, and perhaps that is why their survival stats are higher than ours.
The other thing that really irks me is that having had bc (stage/grade 2, 2 cm, 3/18 lymph nodes +) at my hospital, we only get mammos 2 yrly, and after 5 yrs from dx, we go back into the national screening programme, for 3 yrly ones. Having had a non-palpable tumour, how would I know if I had a recurrence if that was also non palpable?
However, at my 5 yrly review last February, my surgeon said he really should discharge me, but will see me for a mammo and ultrasound next February - perhaps he feels sorry for me? I am just grateful that he cares. Incidentally, when I had a consultation with him after WLE and total axillary removal, he said: “You will more likely die of your Crohn’s than bc, as we can do so much to treat bc and are still in the dark ages with Crohn’s”. Seems as if his words are coming true, as my gastro can’t seem to get my symptoms under control and I am definitely facing surgery soon on the strictures.
Some of my friends, who live in Northants, have been having private mammos since they were in their early forties, as a result of having friends and relatives die “early” from bc. They pay £85…yet when I enquired last year at our local Nuffield Hospital in Plymouth, I was told I would need a mammo and ultrasound, as I had had bc, and it would be £450. I declined their offer. The Consultant Radiologist quoted in the article says that he would also like to see the time gap reduced from every three years to every two years, bringing the UK in line with other European countries and help catch faster-growing aggressive cancers. Why not every year I would ask, as in the USA?
I think Professor Michael Baum’s comments in this article (he is against screening yet led the research on breast-conserving surgery and tamoxifen) is cavalier in the extreme and if I thought the Daily Mail would print my letter I would write to them. Having read some of the posts on this forum, it is obviously a waste of time.
Dr. Michael Michell, in his comments says that over the past 20 yrs the programme has screened 19 million women and has saved at least 25,000 women from a premature death from bc. He goes on to say that when he started working in Breast Clinics at Kings College Hospital in the Eighties, it was common to see women who had aggressive cancer where the tumour was eroding the skin, and that finger-tip examination alone is not a good way to find early-stage cancers. That alone seems to me to be a good enough reason for screening.
Rant over…
Liz.