Hi, My partner of 10 years aged 68 was told April 2019 cancer of the lung, after chemo and radiotherapy in MArch of last year literally just before lockdown that it had worked and he was free of the thing. Then in November last year after being free of it only a short while a phone call out of the blue one evening, the cancer is back, yes a shock, and over the phone , well in my opinion, not good.
After 4 rounds of chemo another phone call yesterday, the chemo hasnt worked, the cancer has got bigger in the other lung. But immunotherapy advised which he is taking.
My take on this is, yes, we know theres this virus out there, but surely the option of actually seeing someone and not over the phone should be given now.
To be told, yet again, over the phone, by a doctor we can barely understand the accent, is i do feel, not good enough.
If theres anyone out there who feels the same please can we all stand up and get thiis out there to the NHS and say, we NEED to see a doctor actually SEE a doctor, so we can understand more from a personal touch.
My partner is a very soft and gentle man and just takes what life throws at him, but sometimes you have to say, im sorry but this is not good enough.
This is what i personally feel.
Does anyone feel the same?
Hi Miss CJ, it seems to be a mixed bag at the minute and perhaps dependant on each NHS trusts individual arrangements through the pandemic. With my dad, who was diagnosed back in August 2020 every important meeting has taken place face to face and follow-ups with the oncologist have been phone calls which has been great actually as its meant Dad hasnt had to treck up and back to the hospital which exhausts him completely. My dads wife however was diagnosed in December and got a phone call to say she had lung cancer which was NOT ok in my opinion. Dads tests and scans and treatment all happened quickly with great coordination but there has been lots of chasing up/following up with his wifes plan post diagnosis even though its all through the same hospital but different cancer teams so Ive almost contradicted what I said in my first sentence. This has been our experience this far. Have you suggested a face to face instead of a phone call because they may be able to accommodate that for you perhaps? Good luck with everything x x
Thankyou for your reply. Everyones differing experiences of this are interesting, but i do feel overall that a face to face is far better than an unpersonal phone call, leaving us both with, well what now? We were given no indication yesterday to consult with a mcmillan nurse either, no guidance on what to do next. Simply to " Book a blood test now!
Good luck to you with dads and his wifes treatment
that's a really good point actually about the blood tests, many were sat waiting at their chemo sessions because they didn't know they needed to have had a blood test before treatment which delays the day by around 2hours and its a long day as it is. I managed to get Dads bloods taken at home every Friday before his treatment on the Monday she it saved him having to get out to the Dr for the appointment which was really great.xx
Hi MissCJ, I believe that is terrible, to be informed by a phone call, when I am sure perspex screening could have been done for the oncologist, When I was diagnosed after an Xray then a CT scan last March, I did see an oncologist for about ten minutes who confirmed I had lung cancer, then later saw a Radiation Oncologist, who told me I was inoperable, in April, since then I have had three face to face meetings, one at the end of Radiation treatment, another when I got Radiation Pnumonitisis, and a follow up three months later, I made an appointment for a telephone consultation with my doctor who I have had for 18 years in, September 2020 he was not even aware I had lung cancer, even though he has had all the paperwork through, unbelievable, my Doctors surgery do not answer the phone, so have to go down and knock on the window to even get a repeat prescription, shop workers have had to see far more people everyday at the check outs and in store, the provisions they have are just perspex, with doctors they could have had perspex ventilated boxes made if they had actually wanted to see patients, no there is no excuse, as far as I can see, radiation technicians have had to see patients for Radiation treatments, My GP is still shut have not seen my doctor for a year now, not that I really want to after he was not even aware I had lung cancer, still have to nock on the window to ask them anything, it is not good enough in your case my sympathies are with you.
Im so sorry your partners doctors are letting you both down. Its not good enough. My husband was diagnosed with incurable nscl last April.
He has had chemo and radio which shrunk the tumour significantly. He remained symptom free until 2 months ago. His cough and breathlessness are back and he is awaiting a liquid biopsy on a lesion found in a inaccessible place in his liver. Bloods sent to the states at no cost as free for research purposes. Expect results next week.
My husband is 73 and has had first class care and we have had face to face oncologist appointments throughout. We live in Scotland.
You could call your partners oncologists secretary and ask for a face to face appointment.
PS, sorry for rambling on. Good luck.
Whatever cancer throws your way, we’re right there with you.
We’re here to provide physical, financial and emotional support.
© Macmillan Cancer Support 2025 © Macmillan Cancer Support, registered charity in England and Wales (261017), Scotland (SC039907) and the Isle of Man (604). Also operating in Northern Ireland. A company limited by guarantee, registered in England and Wales company number 2400969. Isle of Man company number 4694F. Registered office: 3rd Floor, Bronze Building, The Forge, 105 Sumner Street, London, SE1 9HZ. VAT no: 668265007