My partner went through Chemotherapy and Radiotherapy last year after being diagnosed with Throat cancer. All was going the right direction until secondary lung cancer in March...
He has since been on Immunotherapy having had 5 treatments, one every fortnight with the 6th treatment tomorrow. I can honestly say that he is looking better than he did before his initial cancer diagnosis a year ago and although he is still tired and hasnt got the same energy levels the treatment seems to be doing something !! He has a scan on the 14th of June and will see his consultant the first week in July so we will know more then. I know that his diagnosis is Incurable but treatable which is really hard to come to terms with but i think that we just have to make the most of the times he is feeling up to doing things.
For now we are just doing what we can and trying not to think about the future too much but we have just spent the last week doing the North Coast 500 round the North of Scotland which was amazing. He would normally do all the driving when we are on a road trip but this time i drove and he took a turn when he felt like it.
I just wanted to let anyone else know what immunotherapy can do, well at least in the short term as although we are trying to be positive we are also realistic and to be honest Colin hasnt really had any side effects apart from the general fatigue so long may that last.
I know that there are not too many others on Nivolumab but if anyone else can take a wee bit of comfort from my post then that will be a good thing. The side effects were the biggest worry for us both when we first read up on it.
As i read many times, the alternative to having the treatment isnt good so we battle on together through this hoping for some sort of miracle that will give us more time. Without the Immunotherapy treatment the time given was 3 - 6 months.
Thank you for reading, it feels so good to get this off my chest.
Liz
Hello Liz
Thank you for posting such a wonderfully encouraging post.
There have indeed been some excellent results with Immunotherapy and the range of drugs coming on stream and on license is promising.
I'm so glad you are finding great adventures to share and hope you have many more
Dani
Base of tongue cancer. T2N0M0 6 weeks Radiotherapy finished January 2019
Hi Liz
Everything crossed for you and next appointment. It’s good to know and also good for any people in the future to read.
keep on battling through.
Hazel xx
Hazel aka RadioactiveRaz
My blog is www.radioactiveraz.wordpress.com HPV 16+ tonsil cancer Now 6 years post treatment. 35 radiotherapy 2 chemo T2N2NM.Happily getting on with living always happy to help
2 videos I’ve been involved with raising awareness of HNC and HPV cancers
Good evening Liz, what a lovely post to be reading, I don't know much about this treatment so it's wonderful to know there are positives to be had. It's lovely that you are both out enjoying yourselves and not letting Colin's treatment get you down or hold you back, wishing you both all the very best for the future, take care.
Chris x
Linda
Thank you. One thing that i have picked up from this site is the great attitude that everyone has and encouragement that i see you all giving to new members desperately looking for some advice and direction,
Yourself and Dani, Hazel, Chris and others that have replied to my posts so far since joining have really helped me get my head around our situation and find some sort of way to get on with life for as long as Colin is able.
Thank you all
Liz x
Liz
It is great to hear positive news re immunotherapy. I am so glad that it is working for your husband and giving the pair of you a chance for some quality time.
Others will read your post and take comfort and hope that this relatively new approach to treatment may well work for them in the right circumstances. I have other friends with different cancers on immunotherapy and they report similar good progress.
Keep up the adventures!
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