Do they know it’s cancer before the biopsy

Thinking of you today, hope all goes well

Sending hugs
:hugs::hugs:

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Thank you. Waiting my turn for theatre x

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Come back on later and let us know how you’re feeling hope it all goes well xxx
hugs:

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I will do. I know each experience is a step forward but also sharing helps us all. I appreciate all i have read on here too. Hopefully wont be too long now. Starving!

Wishing you all the very best.

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Hope it all went ok today xx

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Hi, I have a further Q! So obviously I was told I had cancer on Tuesday. They told me it was grade 2, pr + and er + but awaiting HER.
I have been given appts on 10th oct for mri and stereo core biopsy, 21st oct for reconstruction options and 22nd October back to consultant once all test results back.
But today I had a call from hospital asking me to see consultant sooner on 15th. Secretary said she knew I was waiting on some test results and wanted to see me sooner so I wasn’t waiting too long. I said I really didn’t mind waiting until 22nd as surely mri and second biopsy would not be back by 15th and to be honest had already been told it was mastectomy and chemo so not sure it could be much worse. She just repeated she’s like to see me on 15th. Consultant is on leave this week so can’t get anything more specific than that. I can only assume the HER result is back or something seen in bloods as they were only tests we were waiting for previously. Anyone have ANY ideas on why they would bring it all forward - it’s really stressed me out this evening!

@worried1
It may be something simple like targets. For instance, patients on cancer pathways have to be given diagnosis and treated within certain timeframes and if your results are back, not only is it better patient care to see you asap, it’s also good to fill appointments and then free up later ones for new patients to be seen.
I was brought forward a few times but they did pre warn me-if we are able to see you earlier then we’ll call you…
Fingers crossed, it’s nothing more than that
X

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Thank you, kind of related but I live in rural Cornwall. My nearest hospital (where I have been so far) is 1 hr drive each way (significantly longer on buses) and some of my upcoming appointment are at another hospital which is 1.5 hr away each way. These two hospitals are where all my treatment will take place. I’m very lucky being a teacher with good sick pay so I won’t lose income initially but I don’t know how I can afford the diesel and parking for the constant trips on top of everything else. It’s £30 a time. Does anyone know if there is anywhere I can look into financial support for this?

I can’t help re cost of petrol but a lot of hospitals give parking permits for patients undergoing cancer treatment so be sure to ask next time you go. I also travel an hour to my hospital and the parking permit has made a big difference as having to go twice a week for bloods/picc line flush and then for chemo.

I also had an appointment moved forward by several weeks and panicked as to why, but it worked out as it just meant everything started sooner and less waiting around. I was also borderline on initial HER2 test so they had to send off for FISH and it came back positive. If you’re worried about why appointment has been moved, have a chat with your BCN. They may be able to put your mind at ease.

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I got free parking for radiotherapy treatment, just had to log in my car registration at reception desk each visit. It made a huge difference because the first time I didn’t know I could drive straight out & went to the machine which charged me £6.

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You could speak to MacMillan for financial advice . I also did not have to pay for parking for radiotherapy appointments - the system was that you take a ticket and pay before leaving but Reception gave a pass on the first day and I waved it at the Security guard who opened the barrier . Some hospitals also offer transport if you’re struggling . One lady at my support group had a volunteer driver - just like having a taxi but she didn’t have to pay him.

You live in a beautiful part of the world - I had an auntie and uncle there who have sadly passed away now but yes I can imagine the transport system is pretty rubbish . I’m in a semi - rural area and it’s not good here. I was fortunate to be able to stay with family when I had my appointments or it would have been 2 hours for radiotherapy and it was a good hour for my other appointments.

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Hello Im back! Sorry for delay in catching up. I did not respond well with anaesthetic and caused them some trouble waking up. Got home at 10pm last night. Slept well surrounded by pillows , bit groggy and sore today. Was sent home with co-codamol but paracetamol is enough.
Yesterday was a very long day. Arrived at hospital at 7am, had radioactive dye in for sentinel node imaging at 9am. This was by far the most painful procedure so far but also not that bad on the scale of things. They injected right next to the nipple to create pressure and then i had to rub it in a circular motion to make it disperse towards the nodes. Pressure went off as soon as i massaged it. All took about 20 minutes.
I went to theatre at 2 and next thing I knew I was in recovery and it was after 5o clock and they had been trying to wake me for a while. I wouldn’t stay awake and threw up. Seems anaesthetics aren’t my thing.
Surgeon came and told me it all went well and that’s all I remember.
Before going to theatre I was examined and drawn on and incision options were discussed. It was a long wait. Another woman was there to have more removed 4 weeks since her last op so that does happen. Just lounging in bed today and have done my exercises and will do again. If i walk around its ok but more sore. I can be very comfortable in bed propped up.
On Friday i see the breast nurse just to chat and have a look. A week later i see the surgeon for results and full dressing removal. I bought M&S surgery support bras and they are excellent. I have to wear it solidly 24hrs.
Its a relief it’s done. I feel like its all over even though its not yet.
Hope you’re ok. Try to live by today. There will definitely be charities who will help with transport but there is also hospital transport Available. Xx


The photo, which hopefully comes through is the tumour with the initial tag in and the seed which was added on Tuesday to help them find the tumour. I asked the surgeon and apparently the tumour looks like the normal breast tissue to the naked eye.

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Dear Square-boob,

Well done for getting this far with your surgery, take good care, lots of rest, good food and be kind to yourself.

Wishing you health and happiness going forward,

With the biggest hugs Tili :pray::rainbow::pray::rainbow:

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Glad you made it home and feeling not too bad today by the sound of it - hope you continue to get well and best of luck for your results xx

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