Please take part in this. Roy Castle Lung Cancer Foundation have fought long and hard to get this adopted to identify lung cancer as early as possible. When you get the letter please contact the number. You will be telephoned and asked a range of questions. Based on your answers you will be invited for a CT scan or told that your risk is low and one is not needed. I have COPD and was telephoned. I was assessed as low risk and nothing further was required. It has no effect on your COPD diagnosis. I lost my husband to lung cancer and wonder whether if this had been in place, he might have been diagnosed earlier. Sorry for the length of this message but as you might expect I am quite passionate about this new initiative.
I totally understand your passion and I'm sorry to hear about your husband. I was always going to engage with the programme but it left me with so many fears. My mother passed from lung cancer and it took a lot out of me.
I can understand how you feel, but the sooner a diagnosis is made the better. I too was worried but after my telephone assessment I was told no CT scan was needed. I do all I can to manage my COPD, which luckily has stayed moderate for many years.
Yes I agree, it can be requested as can a mammogram too. I may bring up the possible lung cancer screening on request for over 74's with my local NHS ICB and see what the answer is.
Like I said, I entered the title line (that started this discussion thread) into Google. A list of hits followed and one of them would be the link you’re interested in. I’ve had a look, but unfortunately I didn’t keep it.
At the risk of being controversial I think that, in some respects, the treatment of elderly people in this country is appalling. They don’t have access to screening programs and help for mobility ( I don’t mean walking aids - I’m talking physio etc) is none existent ( with the exception of the covid vaccine) It is as if they are saying you are on the way out so we aren’t wasting money on you.
I agree with you Troilus. Service for the elderly is appalling. Despite everyone knowing how the elderly were shamefully treated during the pandemic, nobody is shouting out about it
I had a mammogram this year but have been told that now I'm 70 i wont be invited for any more, same with the cervical smears, that ended at 65, its ridiculous as i know people who have had breast cancer over 70, maybe i will have to go private for scans, it does make my blood boil.
It is irritating isn't it, especially when the quality of our lives is still good, despite our lung condition. If you are concerned about about a breast or cervix can you ask your GP?
My husband has had this. He has COPD as he smoked for 50 yrs. The fact that he did smoke was enough to put him through for the scan. His lungs were clear, thankfully, but they did flag up a calcification of his aortic valve. He has an appointment with a Cardiologist next Tuesday so he’s really glad he went for the scan even though he was rather apprehensive beforehand. You should go.
I can understand peaple being anxious bout having things done it's the thought off the results that put fear into peaple but it's best to try put fear facter to one side because if you get chance for anything you go early diagnosis in anything medical issues it better for evertone
The NHS here in Scotland had something similar about 10 years ago or so, for the early detection of lung cancer and I was a willing volunteer aged about 50 then for the CT scans as i had smoked for over 30 years by then and my mother had died with lung cancer being the first of her diagnosis. I was asked after one scan by the radiologist how long had I had COPD . I said i had not been diagnosed, but she commented well it is quite clear on your scan. There was no referral made for further investigations and I did nothing about it until many years later and many chest infections later, my GP referred me for a spirometer test in 2018. Unbelievably, the results showed I did not have COPD by that measurement then. Many more infections the following year and my GP referred me again and I was diagnosed in 2020 weeks before first lockdown with severe (bullous?) emphysema to no ones surprise especially my GP and myself. And it has been downhill since, sadly. Sorry for long post.
Sorry to hear of your painful journey. Its such a consuming illness isn't it, not only physically but mentally too..I do think the tests are a great idea, I was just worried about what they may or may not find.
Hi, I was born with Pcd, and for last few years have seen good consultant who is knowledgeable and helpful about problems caused by PCD. I may ask her about lung cancer tests when see her in September. Jean
I have not been through "NHS programme that checks for early signs of lung cancer." but I have certainly been tested. First was x ray that showed an abnormal shadow, which after CT scans was diagnosed as scarring.
In short testing is X Rays and CT Scans, - Nothing horrible.
I understand this screening is being rolled out in certain areas at the present, including Somerset where I live. Apparently it’s areas with above national average rates of lung cancer that are being prioritised before becoming a national screening programme, it is a different kind of scanner that can detect very small cancer cells in the lungs, before it becomes a problem, from our local news coverage there are only a few of these scanners at the moment. Myself and my husband both had our phone calls. They ask a few simple questions and according to your replies either invite you for scan or not. My husband was briefly a smoker and quit years ago, he does not need scan, I need a scan but as I’ve just had a hip replacement they are leaving me for a few months to recover better from operation.
There does seem to be a push by our local nhs trust for all things respiratory. My town has above national % of deaths from COPD, our health authority have launched a study into all things respiratory in my town, from GPs services, air monitoring and everything else!
I also got an invite a few months back. They found a nodule and moderate emphysema ☹️. I didn’t know about either of these, I’m due a 2nd lung scan next week to see if the nodule has grown. Fingers crossed the nodule is ok
That must be quite unsettling,, i do hope it goes on to be nothing serious for you. Thank you for sharing that and I hope you're being supported well through this.
It should be a lesson to all to get the Lung check done. I've got my first one on Monday, then 8 weeks for the results 🤞🤞
Thank you. Hopefully if it is anything then hopefully they've caught it soon. I had invasive breast cancer early this year, so hopefully it’s nothing to do with that, but if it is then I’ll deal with it.
I guess the moderate emphysema has been there a while though. That has me more worried as my dad had was dx’d with this when he was a young man and I grew up with him struggling to breath each day
Good luck with the scan (if you have one), as not everybody does. They ask a load of questions first and then enter on computer, if you are lucky you get the scan. The scans only last about 5 mins if that and are a breeze.
Went and had the Lung Health Check and scan. After 4-5 weeks I received 3 letters this morning. The first confirmed my Emphysema, they put me as mild but my Spirometry has me at moderate. The second confirmed no lung cancer, thank goodness. The third confirmed Calcium deposits around my heart. I'm already on medication for this.
It was a quick and easy process and would advise everyone to go for the lung health check if you're offered it. Jimmy
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