Hello and thank you for reading
Hello and thank you for reading
Today (06th Aug 2014)
I got my results from the tumor, much earlier than expected.
SUPER NEWS. although it was Cancer and had spread to 1 of the 8 lymph Nodes removed - I don't have to have Chemotherapy.
Because the tumor was so large it grew in a different shape and form and although it has been given it's name as Carcinoma there was a further development.
There were some cancer cells that were not recongnisible and the tumor has been sent to Dundee (Scotland) for further examination to a Kidney Clinic.
It's great that I've been able to share my story, if you have any questions especially if your unsure about the surgery or what to expect. Please feel free to leave me a note. I still have a long way to go as the consultant wants me to have regular check ups.
He was baffled about the cells that were not identified and intrigued to find out more (same as me really)
Thanks
Stew - getting there SU2C
Hello Stew,
We loved reading every sentence of your story - I found it really absorbing! Thank you for sharing it and for standing up to cancer. You went through so much so young and we are glad to hear your great news that you don't need to have chemotherapy.
I am sure others who are dealing with a similar diagnosis at the moment will be happy to read your message and discuss the operation with you. It is very nice of you to offer to help with any questions others may have about the surgery or what to expect after diagnosis. We love your Stand Up to Cancer profile picture!
Best wishes for a full and speedy recovery from the Cancer Chat team,
Lucie, Cancer Chat Moderator
Hello again Stew,
We just wanted to say that we have been talking to our Patient Liaison team about your story and they were interested to know if you would be able to fill out their Share Your Story form ¿ they can get opportunities to help raise awareness in different ways and, although it can be difficult to predict what might come up and what might be suitable, it would be great to know if you were happy to be involved in this way. No worries at all if not, but the form is here.
Best wishes,
Lucie, Cancer Chat Moderator
Hi Lucie,
Thank you very much for your kind words, yes my consultant dealt with renal cancers in the young and said that my situation was extremely rare. I'm going to work hard over the next year to raise awareness in young men and women about renal cancer. Even now I'm still learning about different stages of Renal Cancer? what to expect before and after an operation? How to cope with Cancer? Friends / Family? You name it it's all a learning curve.
Luckily I'm young and fit but I know this isn't the case for everyone and it would be my pleasure to help you where I can
Of course I have a further scan in October and I will see my consultnat later that month to discuss the findings from Dundee - but because it won't change the outcome (as of current) he won't be contacting me to discuss the findings any sooner. I could always ring his secetary if I needed too.
I hope you're well and thank you for kind words once again.
Regards
Stew
Hi again,
tried the link - but it took me to an outlook app and asked me for log-on details.
Happy to help if I can view the form
Thanks Lucie
All the best
Stew
Hello Stew,
I have now fixed the link above - sorry about that I am not sure what happened! It would be great if you could fill the form.
By the way, someone else posted yesterday who was also diagnosed with kidney cancer. You can find puppydog's post here - I took the liberty to mention your thread but feel free to post on puppydog's thread too if you wish. I thought it might be good for you both to talk and share your experience of kidney cancer.
Thank you for your help and for sharing your story!
Lucie
Ta Lucie - I'll have a look at that in the morning.
Good night and thank you
Stew
Here is a summary of a letter I got today from my meeting with the consultant.
I am the partner of someone who at 49, yesterday has just been told that whilst they will and recommend removing his large kidney cancer so he can eat again, the 6 lymph node tumours, small lung abnormality and tiny pin head of suspicion in his hip bone, mean this is incurable and they hope that he will live for a further year to two years with good pain management. Very confused at the moment as we thought that the removal of the kidney plus immunotherapy therapy treatment COULD cure this
Wow dude... my experience is so similar. Loved every word you said. Except my postcode was G2pTa TCC basically bladder cancer in my kidney
My experience with surgery and recovery was very well. But the vagueness from the doctors is so stressful last year I went to pals just to finally get answers. No one told me anything till my cystoscopy 4 weeks after ct scan. One year later and I go in for a checkup was told to get antibiotics because I have an infection.... that was 6 weeks ago. 4 weeks ago I had a ct scan. Then that day they sent me out a letter asking me to go in for another ct scan? For this Friday.... guessing that’s a mistake. It all feels like a repeat of last year not a call or letter. And stressing.... but I can take it! If this was my mother or relative and they get just the same treatment... I’d go absolutely crazy!!
Sorry my English is soooo bad
wish you luck buddy