Hello
I just wanted to talk about a couple of things. To see if anyone has same experience. Or if it helps other people...
I am 39, I had a lump in my breast, no pain, small dent. I went to the breast clinic on Tuesday, from the mammogram and ultrasound alone the nurse told me it was cancer and she was doing the biopsies not to rule it out but to determine grade and stage.
This worried me as of course I assumed it meant if it was really obvious, it was the worst case scenario, death sentence cancer. I spoke to a wonderful Macmillan nurse when having a total meltdown and she assured me this is not the case. It's just characteristic. It looks like cancer, not a cyst or fibroadenoma etc. It doesn't mean it is game over.
The clinic nurse said it was early. This surprised me as she says the lump is 2.5cm which seems big to me. I asked the Macmillan nurse what "early" meant and it is related to size.
I was scared about all the stats saying that women under 40 more likely to get an aggressive cancer. But the nurse explained the data is so skewed here... it looks worse because younger women don't get regular screenings. So it's often caught later. That has helped me.
My biopsy result appointment is 20 Jan, which seems like forever away. Surely if it was an extremely aggressive cancer I would be called in earlier? I don't know how these decisions are made, who to prioritise or not.
I have convinced myself I have secondary breast cancer or inflammatory breast cancer despite having absolutely no signs it is elsewhere in my body. I feel fit and healthy. No weight loss. No vision problems, digestion, back pain, yadda yadda. I feel absolutely normal.
I read an article by Diana Henry (Telegraph cookery writer) where she had also convinced herself she had the "worst" kind of breast cancer. When she got her diagnosis and she found out it wasn't, she came home and opened a bottle of champagne!! Ha ha. It is so weird to be hoping for a "common garden" cancer as I have been calling it.
The clinic nurse took 3 samples of only one lymph node. She said it was equivocal - could go either way. Surely if it is in one lymph node that's better than multiple? And doesn't mean it has necessarily spread beyond?
When I first heard the news I of course thought the worst and signed my death sentence. Awful visions of 80s tv of mega sick people on chemo. I know now the menu of treatment is so complex and diverse and I might not even need chemo, and if I do lots of people manage to have normal lives, and continue to work, on it.
It is extremely emotionally draining telling people. I want a button that just inserts it into peoples' brains - they can acknowledge it or not, I don't care. I just want people to know because hiding it takes so much energy from me, energy that I need to fight this.
I think the emotional recovery will be worse than the physical. The huge fear that it will come back. By none of us are 100% risk free... even people from general population without a diagnosis.
I will be treated in a hospital that is a national centre for excellence. I am grateful for their expertise and experience.
I am constantly moved by the kindness of people. It is too much.
I am desperate for this not to define me. Someone I know described their cancer as a "mending journey" - I like that. Something is broken - we will get it fixed - we move on.
Has anyone watched the tv show Cheer? I have been saying their chant:
We can, We will, We must
Anyway just some thoughts. Thank you everyone x