It's world Head and Neck Cancer day today.
Macmillan asked us Community Champs to contribute something to their Community Blogs.
Here's mine. Mike has one being published soon too.
So many people don't even realise the Community is here. I do wish our teams would signpost us not only to all the general support Macmillan can offer, which they largely do already, but to this group where we can help each other. I'm going to share this on the social media platforms I visit and tag my cancer centre and oncologist. Have a read and if you think you could share it too it might help a new patient find us.
(Some of you might recognise the odd quote)
shared..
Loz (61)
Oropharyngeal right tongue base T2N2bM0 squamous cell carcinoma p16 positive..
Hi Dani
It is exactly the same in Australia. Our medical teams do not alert us to the existence of Head and Neck Cancer Australia or the more general Cancer Council that also provides support for head and neck cancer patients. No one in the hospital when I had my ops alerted me to these organisations either. I had to search the internet when I felt I needed peer support after my second op for jaw cancer. I was so lucky to stumble across the Macmillan site and then found this great group. It has been a godsend for me. I have since found the 2 organisations in Australia that I mentioned previously and have joined them. However I still find that I get the most support and info from this forum. If only our consultants would give us info on where we can get peer support as they are our first point of contact.
Lyn
Sophie66
Thankyou. The more the merrier. I tagged my oncologist and he’s reposted it too.
Dani
Base of tongue cancer. T2N0M0 6 weeks Radiotherapy finished January 2019
Thank you Dani these are great reflections on this hugely positive and inspiring forum.
I couldn’t agree more that guiding people towards peer support is so helpful and supportive. No one understands better than someone who is sharing the experience.
i don’t want to burden my family and friends and I think most have put it behind them. I still have lots of uncertainty and fear and I find my reassurance here.
Thank you to all of you who regularly contribute it means so much.
Thank you to all of you who regularly contribute it means so much.
Thanks Joli93
that means so much.
I’ve battered all my X contacts with this today. I’ll use Mike’s when that’s posted too.
Dani
Base of tongue cancer. T2N0M0 6 weeks Radiotherapy finished January 2019
Thank you too Dani....it should be shouted and and applauded.
Joli93 mentions that no one understands better than someone who is sharing the experience ! So very true and thank you to Joli for her support and Dani you bring so much support to us all.
Thank you
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