So sorry to hear that Emkins, but glad your mother is feeling well, I went vegan, stayed 100% positive, kept active, took cannabis oil, it is herbal doesn't send you high, and had chemo the doc advised, mine was non small cell, in my lung and spread to lymph nodes and bones. I found to think of where I'd been and what I've got, children and grand children, rather than thinking what I might be missing out on in the future, I found that a great comfort after having a terminal diagnosis.
Thank you, they told me I had an average of 12 months, last Oct, and my scan results this March showed my cancer to be inactive, at the moment anyway, Januarys scan showed the cancer in my bones was dying and the tumour had shrunk slightly.
My thoughts are also with you Emkins. I had non small cell 2 years ago and it was contained and tiny. I feel blessed and have changed my diet to exclude meat and lots of green veg. Stress I have found is the difficult one to avoid ! I wish you all the very best.
I had a right upper lung lobectomy using VATS surgery. The tumour was contained and had not spread anywhere else. I was very lucky indeed as the first Consultant kept advising it was infection. I found I had to be really assertive and an advocate for myself. I do not have any treatment, but have had to fight for the hospital of choice aafter I lost confidence in the original one, and more regular CT scans.
That's a thing - many of us look very well when diagnosed so it's a shock to all. sorry to read about your mum. Please be careful when looking at the info on the internet - it is outdated, and averaged over many years when treatments were not so good. In the last few years treatment options have changed in every mode. In Dec 2010 I had left upper lobectomy and diagnosed in Jan 2011. At that time everything I read was very negative but I decided I was going to aim to be in the survivor statistics! Although I don't accept any of us are statistics I read a couple of great books - 'anti-cancer a new way of life' by Dr Servan Schreiber and 'cancer is a word not a sentence' by Dr Rob Buckman. Both helped me understand better. I am very involved in lung cancer research groups and regularly attend cancer conferences and wish I could bottle the energy, enthusiasm and commitment clinicians and researchers have around the world to try and improve outcomes for lung cancer. Do not give up - create and sustain hope and create memories and make the most of life. There is trusted regularly updated information on Roy Castle lung cancer foundation website that is written in plain English and reviewed by patient review panel. This can help explain treatment options and the difference between lung cancer types. Treatments that patients may have for non small cell lung cancer can be very different from those for small cell. It's important to discuss with your mum's clinical team about her specific situation as the tumour biology (pathology can determine this) may affect her treatment options. Good luck.
Thanks so much.. we’re already planning good things ahead and being as positive as we can - although a lot of it is denial on my mum’s part. If that keeps her positive though, I’m more than happy with that.
We haven’t seen her oncologist yet, as I spoke to the lung cancer nurse who confirmed small cell stage 3a.
I hate the unknown and knowing how aggressive this can be and incurable.
I will look out for treatment options as I’m acting on behalf of my mum as, like I said before, she’s not really recognising what’s happening so I have to be x
Yes I agree. I had no symptoms and it was found by accident. There is so much conflicting information, especially around sugar ! I am trying to get on with my life and not living a life all consumed by what happened and concentrating on where I am now. It is only part of who I am not all of me.
There are positive stories out there as you have read and hopefully things will be more clearer once you have had the consultation with the specialist.
Your Mum is lucky to have you and do make sure you take care of yourself also.
Thankfully there are advances being made in lung cancer and treatment options are slowly improving.
Hi sorry to here about your mum I had stage 2 had top lobe of lung removed I also had it in nodes had chemo which was not as bad as I thought and the nurses are second to none they go the extra mile to help with any side effects I am now fine and have been for 18 months hope this helps your mum and I was not a good candidate for surgery but got though it with no problems good luck to your mum xx
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