I was diagnosed with right lung cancer a year ago. The doctor told me I had been lucky as I had developed the cancer at least three to four years before they told me. I'm told it is a slow growing cancer but that is all. Does it have a name how does it progress is there symptoms that I can look out for that will indicate how quick or slow does it keep on growing.
I was told that as I have ischaemic heart disease and coronary heart disease that the tumors are too close to my heart to have surgery or even a biopsy and for those reasons chemo is also unsuitable so I have had a course if I think radical radiotherapy at the beginning of the year. The treatment has damaged my oesophegos and it has left a lot of scaring on my lung so they were waiting for time to pass till my next mri scan to see if there has been any improvement. Had one face to face visit to see the oncologist and now expecting a phone call appointment in December. So I think it's been hard trying to work things out as to what if anything I can do to improve my quality of life. I also look after my husband who has Parkinson's Disease and an older sister with Alzheimer's. So sometimes life is hard. Anyway that's it for now my best wishes to you all.
Hi Mammaduck,
Welcome along.
I also have lung cancer (although mine is left lung) and have recently had a large tumour removed along with the lower lobe and some lymph nodes, and am just about to start chemo.
I think it may be difficult for anyone to tell you which type of cancer you have without having a biopsy / pathology done on the tumour?
I was told mine was a slow growing type of cancer, and was identified as Adenocarcinoma after a biopsy, and prior to my Op. Am sure along the way one of the specialists said it could have been growing for "years". I had absolutely no symptoms of cancer prior to being diagnosed and my tumour was 68mm (which in old money is between 2 and 3 inches in size).
Obviously your MDT are better equipped / informed to answer your questions, or even your specialist cancer nurses if you have access to them?
All the best in your treatment and fingers crossed the radiotherapy has made a difference.
Take care.
Dave x
Thankyou Dave
I have a telephone appointment on the 5th December with my specialist nurse so hopefully I'll be able to ask questions then. As from what I can remember I have two tumors around 2-3 inches in size l hope your chemo goes well stay strong and keep smiling xxx
Hi Dave hope your treatment is helping and you make a rapid recovery. I'm scheduled for a CT scan on 11 th January so hope I can get some answers then. The MN said they couldn't tell me the type of cancer as they are unable to take a biopsy or let me have chemo. So it all depends on the scan results. Anyway I wish you well and stay strong xxmammaduck x
Like you, I had a tumour which must have been there for quite a while before it was discovered. It first showed on imaging in January 2020 but wasn't biopsied until September 2020 as I was having chemotherapy for lymphoma. Even prior to biopsy, we knew it was slow growing because no significant growth was showing on the scans.
Although I did have a biopsy in 2020, my tumour wasn't surgically removed until April 2022. It was slightly smaller than it had appeared on imaging and it was low grade with no spread to any nodes.
As I'm sure you've been told, radiotherapy causes inflammation which can make it appear that a mass has increased in size.
You will be monitored for many years to come and your team should have told you what things should have you contacting them to bring forward your next appointment.
I hope your 11 January scan helps clarify things for you and I would definitely recommend talking about any concerns you have with your team at the follow up appointment.
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