Hi all
I’ve been reading many posts as I wait for my results and have found the messages helpful so I thought I’d write as well, even if it’s just to get things off my chest.
I’m 39 and have family history of breast cancer (paternal aunty). I saw my GP on 2nd May because I felt a hard painless lump in my left breast and went to the breast clinic on 15th May. When I saw the consultant before the tests she told me that although the lump was hard and not moveable it seemed “fairly innocent” and that it could be a result of the lactation (I was still breastfeeding my 2 year old occasionally, not anymore). I had an ultrasound and a mammogram, then a biopsy of lump and armpit, I was inserted a titanium marker and then had another mammogram. At some point in this process the radiographer and nurse suddenly seemed different and asked me several times how I was even though I was feeling pretty calm… they were absolutely lovely but somehow it felt as if they were offering some reassurance I hadn’t really asked for so I started to feel a bit suspicious. The consultant then said they had “some level of suspicion” but that if it was cancer it’d be very treatable because the lump was 1.5-2cm and that I’d receive the results at a face to face appointment in 2-3weeks.
A few days later I received an appointment letter for the 20th June (5 weeks later!). I thought perhaps the long wait meant low priority = good news… but I called the breast care nurses and I was told they didn’t have my results yet and that unfortunately that’s just how long is taking for everyone to have a follow-up appointment at the QE hospital in Birmingham at the moment… They also told me that I wouldn’t be able to receive the results over the phone or through my GP but advised me to call in 2 weeks, when my results were ready, to see whether they could bring my appointment forward if there had been any cancellations.
I called the number they gave me last week to speak to one of the surgeons’ secretary and left a voice message. I got a call back as I was driving in a rush with my two young children in the car so I didn’t really feel like I could think very clearly or ask questions that I wish now I had asked… the secretary said they had my results and that they had “discussed” them… does that mean at a MDT meeting? And that they could offer me an appointment for the 16th June (4 days before the initial one). I think she also said that they’d call me if they had any more cancellations but by then my brain was a bit frazzled…
I think I was doing pretty well in terms of remaining calm and trying not to think about it much but today I feel all the bottled up anxiety is hitting me…
I’m sorry I’ve written such a long essay… but it feels good to share. Has anyone experienced such a long wait just to receive the results? Is anyone receiving treatment at the QE at the moment? Are delays as this common at the moment? Do all biopsy results get discussed at a MDT or just positive/uncertain ones? Should I call again to see if there have been more cancellations or will they notify me if there have? Arrrr I just can’t stop reading into all the interactions I’ve had with the doctors and nurses… and it’s not helping.
Thank you for reading :)
Hi BrummieAl welcome to the forum..Stop, Take a big deep breath and let it out. Just from what you are saying and all the elusive interactions you have experienced it sounds like it could potentially be something they weren't expecting. All results go to an MDT and are discussed by a wide array of professionals all making up a breast care team. Once those results are known you will get an appointment to go and see them. Dependant on where you are in the country times for this do vary and it sounds like you are experiencing one of the longer waits to be seen. You are not alone in feeling as you do and the secret is to keep super busy to pass the time. The 16th is a week away now so not long. Some people find it helpful to take someone with them to this appointment as two sets of ears are better than one if that makes sense. Please keep in touch and don't overthink it(easier said than done I know) you will drive yourself crazy and that's not good. Sending sone huge big hugs your way for now and thinking of you.
Hello and welcome to the forum! I only joined last week but I have found it helpful, I hope you do too.
I was diagnosed with HER2+, hormone negative, grade 2. Lump is <2cm but spread to at least one axillary lymph node. I’m having a CT tomorrow and an MRI scan hopefully soon too. So not grest news but I honestly feel so much more in control now that I know.
How long have you been waiting and when are you supposed to get the results? I really hope you can get them soon because that uncertainty can be really hard. Please know you’re not alone - thinking of you and wishing you the best xx
Thanks for taking the time to reply. I’m sorry you received the results and now having to deal with this. Please remember the Consultant’s words about it being small and treatable.
It feels like a lot of Medical terminology and classification to suddenly try and get your head round.
I hope your CT scan goes soothly (though appreciate it’s another stressful thing to go through)and results nice and quick, then a proper plan can be formulated. I’m rooting for you.
My results are tomorrow morning.
xxxx
That sounds very prompt, which is what we want. I hope you found the scan ok? And hopefully you can chill a bit (if that’s possible this weekend).
I was told today I have dcis, small, lumpectomy and probably tablets.
Though surgeon then said there was a different area on same breast that has been flagged up and I’m having a biopsy next Thursday, when those results come in (hoping and praying it’s nothing) a decision will be made. Surgeon and breast care nurse lovely. I must admit I cried a bit, but appreciate so far I’m in a good position in a horrible club full of lovely people!
I’m sorry I’m only replying now, it took me a while to find this message thread … and I’m very sorry to hear you didn’t get good news either. Good to hear that is not invasive but yes the uncertainty of having to go through more tests is stressful and I’m not surprised you cried… I’ve had my moments too and I’ve actually found crying relieving.
I’ve had my CT and MRI scans already and I’m seeing the oncologist on Monday. The appointments have kept my head busy and I’m glad I’ll see the oncologist soon, so I’ve been Ok. I just feel really fatigued… I have been feeling unusually tired for a long time now but I guess the difference is that I kept brushing it off whilst I’m now trying to listen to my own body and rest as much as I can.
How have you been feeling in the last few days?
Hope the biopsy goes well tomorrow. I’ll be thinking of you and praying the results come in soon for you and that they are clear xx
Hi
no bother xx it’s a lot to process, appointments, telling people, looking at different forums.
Will the oncologist on Monday give you the results of the ct and mri scans? How do you feel about that? It’s funny how you can look back at little signs and symptoms but they can so easily be put into the category of busy life, stress, normal physical aches…
TBH I’m still feeling a bit tender from the first biopsy , surgeon said he could tell I had a hematoma there as I flinched when he examined me. God knows how I’ll get on tomorrow. I’m also planning on going to Italy the next day, the BCN encouraged me and said I might as well. With the sensations I’m now acknowledging in my breast I hate to say it but I wouldn’t be surprised if they said I had something invasive. I will just have to wait. X
Hi! I think the oncologist should have at least the CT scan results which will confirm whether or not it’s spread beyond the armpit… I have to stop myself thinking about it too much… so I am glad I’ll know in a few days, whatever it is. And yes, I had the feeling that this level of fatigue was strange… but as you said I just put it down to having a busy life with two young kids plus perhaps some hormonal stuff… cancer never even crossed my mind! or at least not until I was referred to the breast clinic…
How was your biopsy today? When will you know the results? Hope this time the recovery is easier and that you’re not in too much discomfort and still looking forward to your holiday. Italy will be a great distraction! I found the wait for the biopsy results nerve-racking, and this being your second time and if you’ve got some suspicion… it must be pretty hard. So I agree, the best thing you can do is to try and disconnect and enjoy some lovely sights and tasty food in the sun :)
We had booked our holiday to Spain (I’m Spanish so it’s our summer ritual) for the end of July but we’ve cancelled it already as I should be starting chemo around then… anyways all I want now is to channel all my energy into getting ready for summer 2026!
Hope you have a nice time in Italy - I’ll be thinking of you xx
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