I am sure my post is similar to lots of people who have been through this, the words that I use I am sure have been used several times before. My situation is similar to so many others so why do I feel so very alone!
Confused
My story starts 5 weeks ago, where I rolled over in bed and my arm brushed down my side and I found a lump ! I remember that night well, a cold shiver down my spine and a fear creep through my bones, I phoned my dr the next day ... No appointment just a telephone conversation… I was told I would be referred and if I had not heard anything in 2 weeks to ring the hospital for my appointment. I was told not to worry, it’s probably a fatty lump, it’s probably because your close to the menopause, it’s probably nothing, I waited for 2 weeks and heard nothing … normally I would have left it another week but I didn’t. On phoning the hospital I was told my GP had not referred me ! They hadn’t done the referral! Thankfully the lady on the phone was lovely and dealt with it, she also told me there was a 6 week waiting list and I was now already 2 weeks behind that! She was lovely and got me into another hospital over 50 miles away from me but a much shorter waiting list. I was in for the following week. I was able to put it to the back of my mind … but then my son came down with covid! Self isolation for us all and luckily I didn’t get it. But my appointment was put back another week. But that’s ok … it’s just a fatty lump isn’t it?
Frightened
Two days before my appointment I tried to find the lump again, it had disappeared! Gone ! I felt elated … but then I did a bit of dr google and read forums … it said do not cancel your appointment! The day arrived for my appointment, I had told no-one, didn’t want to worry anyone. I was alone. The oncologist was lovely and at first she missed the lump she had to move my arm to the right position to find it, but as soon as she felt it she was very matter of fact and straight to a mammogram. Paula was the lady in there, and that’s when it started feeling real! I wouldn’t be here if they thought it was a fatty lump would I? The tears came but she kept me calm and just talked to me. It was then onto an ultrasound and then she told me they were going to do a biopsy …. 2 actually another lump was found on the ultrasound. Paula was there when the other dr did the ultrasound, she help my hand when they put the anesthetic in and did what they needed to do. I was then sat outside waiting for the oncologist. When I was called in she told me that she found a lump and it was suspect and that’s why she sent me for the mammogram and ultrasound. She then tells me that her suspicions were right and that I have breast cancer … I just look at her in disbelief… I ask her how big it is and she said that it is between 2 and 2.5mm stage 2. I have to wait till Thursday for my biopsy results and then we will have a plan. She also told me that I needed to start telling my family members. I don’t remember my journey home.
Time has stopped
Today is now Saturday and it seems a very long time till Thursday, I am so up and down right now, I have read so many things that say cancer can’t be diagnosed until you have the biopsy results and think that maybe the oncologist has got it wrong. But then I think that I am going to be given the worst news one can expect as she has already diagnosed me without the biopsy. I want Thursday to hurry up and get here … but I also don’t want it to get here. My kids are 21 and 23 and awesome, I have told a few people but I never ever realised just how alone you feel. How dark it all feels and how hope is very far away at this stage,
like I said I know I am not alone in my thoughts, I know hundreds have felt the same as I do … how do you get through it all. It feels my whole world has stopped and I have no idea how it’s all going to start again …
Welcome to a place where you probably didn't want to be but firstly, I would say well done for joining as you won't be alone here. Virtually of course but I have met some wonderfully supportive people here despite us all at different stages of surgery, treatment etc. It can be a frightening place but you'll manage to plod along like the rest of us as for me it meant surgery, my cancer is gone but radiotherapy starts next week to make sure. Read my profile by clicking my name.
In these times with minimal people allowed in, I too had my exam, mammogram, ultrasound and biopsy on my own. I had to return a week later for results and was not expecting what I was told (although the foreign European registrar had a lousy manner and kept referring to this lesion and did not mention the word cancer once). Unfortunately things do take time but in some ways this is good as it means they are discussing your case and putting a good plan into place.
You can't change your results and so try and focus on other things to keep your mind busy. Write any fears, questions etc down so they are out your head. The waiting game is not a nice game to play but we all get roped in anyway. Cancer is very treatable these days. Your emotions will be all over the place and thats OK too. Its a lot to take in. Perhaps take a pen and paper when you get your results so you can write stuff down. Tell who you feel you need to tell. some people will react well, others not but thats not your concern you need to do what you feel is right for you.
Feel free to post in here. We've all been in that position before and its not nice.focus on the good things for now. Thursday will soon be here and then you have a plan of action. Good luck and let us know how you get on x
Hi, so sorry about your diagnosis, but I can assure you, this website is great for support! Your initial diagnosis sounds like mine, referred with a lump, ended up with mammogram, ultrasound and biopsy at the same appointment with an immediate “pretty sure this is cancer” at the same time.
I do have to warn you that the waiting, and there is a fair bit of it, is the worst. Once you have a full diagnosis (who knew there were so many variations of breast cancer) and a treatment plan, then it does, bizarrely, get easier. And you will get through this, just like thousands do every day. For me there were good and bad days, but generally all quite manageable once treatment started.
If you're interested, check out the blogs on the blog page (mine is One Life Live It) as these can be useful for seeing how people have coped. And try to avoid Google, it's really not helpful. Best of luck for this week x
Hi I know exactly how you are feeling. You are going through the worst part of this whole process. It sounds like you are about my age and are children are also about the same age - I was very grateful that were as old as they were and not young children.
like you I did most of it alone for the same reasons as you. To this day my side of the family don't know I had breast cancer. My children I only told the night before surgery so that they would only worry for one day as the next day it was going to be removed and gone.
My cancer was grade 2 as well and was all removed during surgery January of this year. After surgery I had radiotherapy and now I am on Tamoxifen for a couple of years as I am pre menopause and will probably switch to the post menopause tablets in two fish years.
Grade 2 isn't bad and hopefully it will all get removed during surgery and then you like me will be cancer free.
It's stressful I know but these days breast cancer is very treatable with very high success rates especially when caught early which yours like mine seems to have.
Keep yourself busy so you are not imagining worst case scenarios and DO NOT GOOGLE as the information is often outdated, the worst case scenarios because those are the ones that make 'interesting reading' or just plain wrong.
You will get through this.
If you need to talk keep posting on here and you can always message me and I will reply.
Wishing you all the best with your results x
Hello Slidingdoors. Although your experience is different to mine I do know what the waiting is like just like others with more experience have said. It’s just awful. Even when you get good results it’s still awful waiting for your treatment plan. I do know from being in this forum that members are only to willing to help and support so you’re definitely in the right place. I’m sending virtual positive vibes and hope they work for you xx
Hi
I’m in a very similar place to you at the moment and thought it might help to let you know I know how you’re feeling right now. Yesterday I too was diagnosed without the biopsy results and now waiting to see the surgeons….I have some moments of calmness and acceptance and then feel completely overwhelmed and panicky and thoughts are running wild which I’m sure yours are too. I hope these feelings pass and we will both feel better when things start to happen. I was really expecting it to be a cyst and didn’t go to the GP immediately because mine is a smooth lump and I had a few weeks when I wasn’t sure the GP would even find it so probably delayed by about the same time as you. It’s the waiting that’s so awful.
Good luck for Thursday. I don’t have a date yet and it seems like a very very long weekend but I’m trying to take the positives which were ‘it’s very treatable’ and I’m sure that applies to you too x
Hi Slidingdoors and Wobbly1, so sorry to hear both your news, waiting test results for cancer is the most scary place to be, we have all been there so you are not alone, all the lovely ladies on here will understand how you feel and when you know your treatment plan the chances are that someone will have been on the same plan and be able to offer support, I had chemo, lumpectomy, radiotherapy and targeted therapy, some start with nthe op and then move onto chemo or radiotherapy, Thursday will come soon enough anf you will then start to find your path and all on here will try to help you both. Lots of love Ann
Ty for taking the time and reading and then taking the time to reply. I am hating the part where I am not in control in more ways than one. I have an added issue where I was diagnosed with a rare heart condition November last year and have had one operation for that and am needing another, so my whole world seems to have fallen apart with this diagnosis as you can imagine. Baby steps. I will have a read if your profile x
Aww sweetie it’s really hard isn’t it. I wish you the best and fingers crossed. What I didn’t add in my last post is I was diagnosed with a rare heart condition last year, I have had one operation and am having another so this is really the icing on the cake for me as I don’t know how the treatment is going to effect my heart or even if they can fully operate. It’s a bit more complicated for me and am going to have to have consults with my cardiologist as well. In some ways it comforting to know I am not alone in my emotions and feelings, and it’s ok to feel like this, but it’s awful to go through. Hope you get a date soon, please let me know when you do get it x
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