This website uses cookies. By clicking Accept, you consent to the use of cookies. Click Here to learn more about how we use cookies.
- home
- Forums
- Information and support
-
Blogs
Share your story in our online journal space.
- Online Support Groups
Turn on suggestions
Auto-suggest helps you quickly narrow down your search results by suggesting possible matches as you type.
Showing results for
- Cancer Connections
- :
- About Buru
Buru
New Contributor
3
Posts
0
Hearts
Turn on suggestions
Auto-suggest helps you quickly narrow down your search results by suggesting possible matches as you type.
Showing results for
since
July 2019
July 2019
Turn on suggestions
Auto-suggest helps you quickly narrow down your search results by suggesting possible matches as you type.
Showing results for
July 2019
Thank you for your reply. Thats just it the more I read the more I think they are not giving me all the information. All I have so far is the name. The staging appointment was huge for me, I guess for us all. But I didn’t get a stage. They didn’t make a connection between the things going on that I have linked easily by reading. There is a formular I found they use to know what a safe margin is .02mm is not enough it should have been 5mm. Then they didn’t get the second time right either. I don’t think they are giving me all the information because they have not things right. My issue now is I am stuck with a team I don’t have much faith in.
... View more
July 2019
This starts with a squamous cell carcinoma cut from my back. Some time later the same cancer grows in my left toncil. I am waiting for 2 more surgeries one to get nodes in my neck the other to get what was not taken by the first surgery. My question is about the information I get from the doctors. I get a very strong feeling that I am only getting the PG version and being told only what they think I need to know. Even though I have said this to them. Dose anyone else feel that this is happening to them. They don’t seam to make a connection between the cancer on my back and the tonsil cancer. In fact the doctor said my back was basil not squamous although I have a report saying 7mm 6mm squamous the Doctor who took it only took 2mm in depth. On my pet scan the glow is rather large but they say possibly a small spot. In all from my first visit to an ENT specialist to my next 2 operations will be less than 40 day. Yet they saying don’t worry . Am I over thinking this.
... View more
July 2019
I have just been told I have cancer and don’t really know much else for sure. I do know that already it’s a very lonely gurney. One thing that dose keep rolling round in my head is how those I hold close will be affected not only by my passing if that happens, but more so watching the decline. If you think you can handle that chase him. I don’t know but it I believe it will be a life changing time for you if you do though. I am very lucky I have someone who will be there with me no matter the outcome. Still either way how do you ask any one to watch you be consumed by this. Dont know if that helps.
... View more
Latest Tags
No tags yet
More information
Join the community
Cancer Council NSW would like to acknowledge the traditional custodians of the land on which we live and work.
We would also like to pay respect to elders past and present and extend that respect to all other Aboriginal people.
© Cancer Council NSW 2024 Head Office Address: 153 Dowling Street, Woolloomooloo NSW 2011.
Cancer Council NSW is registered with the Australian Taxation Office as an Income Tax Exempt Charity: Charitable Fundraising Authority No. 18521.