Breast Cancer : my name is Tracey I’m... - My Breast Cancer ...

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Breast Cancer

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my name is Tracey I’m scared.

I turned 50 in December so got a routine Mammogram request in March. I not having any lumps wasn’t going to go I planned to put it off. But a voice inside said “just go get it over with”. I’d had one before in my 30s so knew what to expect. That was just lump but hormonal changes so all sorted.

So off I went to a supermarket car park screen thing, had the mammogram thought I get the all clear and that be it.

sadly that wasn’t it. I received a letter few weeks later saying I had an appointment at local hospital but not one that I usually go to. Breast Care Unit. I went and told I needed a biopsy and told to return few days later.

Then the results delayed by two weeks due to pathology department, apologies made by then and I told I could complain but I said no point no one’s fault. So I waited.

then I went back this week and told findings of suspicions of cancer. My husband asked is it cancer and told it’s very likely. I didn’t ask questions I told another biopsy must be done this was Tuesday this week. Larger area taken. And now we wait again 3-4 weeks for results delay in pathology still. Which is no one’s fault but the waiting is I finding the worst. I constantly googling breast cancer and treatments. Options.

I have had cancer scares before but always gynaecology I already have a watch and wait problem with gynaecology so I never thought for a moment i be told breast cancer. This has completely frown me. If told cervical or endometrial then I’d say ok had these probs before. But breast cancer!! Now I’m concerned I be told next my watch and wait problem with Gynaecology be the next thing. My head is all other the place. But my husband who did get emotional in the appointment says let’s wait and see his life motto, and yes that’s all I can do but I don’t want this I’m not ready to die yet, that’s what’s going round and round in my head I’m not ready yet,

My daughter is 18 she has ASD life social skills is hard for her. Friendships hard for her.she knows I might have cancer and I can’t tell how she is feeling she’s very matter of fact. But I also know she will be feeling in her own way and panic attacks a thing she struggles with. I’m now pushing her to go to cinema with her dad not me. Using the excuse I hate scary movies. That part is true!but there relationship isn’t as it needs to be if I not around. He will not think going fishing not ok every weekend thinking she’s 18 & be ok. My daughter has another family another set of parents the birth parents. I’m helping make connections to the one parent that we told never hurt her. It’s important to support her but with me not here she will need support and guidance I just worry my husband won’t be supporting in the way he should. He could loose her completely and that will be heart breaking, she could choose her birth father and although I know that’s good for a relationship I’m also very conscious of why he didn’t get custody in the first place. I’m not ready to have this. I’m not ready there’s so much I need to help my daughter with first.

ok I don’t know yet the full treatment plan I don’t know if my cancer is…

All I keep thinking is what if this what if that. And that I’m not ready!!

I did always think I get cancer with all my other gynaecology problems, but with the scares & watch and wait. and then nothing I thought it wouldn’t be yet. Not yet.

plus my dad two falls two operations to his knee and can’t drive let alone walk in knee brace age 80 but thinks his 21 and invincible and says when he driving he be off out! My mum constantly crying over her parents who passed away several years ago my grandparents. My mum cries and still grieves there lost. And every anniversary birthday and anniversary of their passing is met with more anger more tears. Regrets and all. So my mum needs a lot of something which I always get wrong but she needs time and understanding. But if I unwell what then. And my sister has a bone disorder degenerative my parents were her carer with my sisters husband. my brother in law got MND diagnosis few years back I not helped as much as I should I admit. But since my dad s falls and unable to drive I now take them all to there hospital appointments. I’ve never driven to some many different hospitals in my life before. I’m now the main one who called upon only one left to help. But how do I now with this diagnosis looming over my head.

and to top all this I have two jobs. A relief mental health nurse which I only do enough to keep my PIN number going. My main job is a foster carer me and my husband a family thing not some thing one person can do alone. My husband works full time but also a foster carer. My daughter helps out too good at making chicken nuggets and chips when needed. A family together foster caring at present an angry mostly little boy age 10. His settled well as settled as they can be his been here a year. One whole year we survived each other. His not our first child but first been here a year. But now cancer we asked or rather I asked will he be moved. I’m told we can wait to see what treatment plan first if chemo then of course even I know he cannot stay here for his as well as my sake. But if cancer early stages and no chemo I’m praying my treatment plan with medication and removal of the area, my head full of please let that be it even if just for now!!

but I’m not getting a gut reaction or anything to think I be this lucky, as for mental health nurse registration I can sort that out with advice.

my husband keeps ringing to check on me in the day when his at work. Very sweet but this is not normal most days we get on each others nerves as been married and together a long time. Life up and down as life can be. But we had so much years of infertility the ivf the donor eggs the gynaecology stuff. And now age 50 breast cancer and not even a scare nope I go all out and now told no matter what 2nd biopsy results the area will need cutting out!

noooo noo I’m not ready not yet. Fine give me cancer if the breast but not now. I not ready now I have so much to do and people rely on me. Please not now. This is what’s in my head.

Of course I cannot change what happening but my head is going round and round.

Daily I must be good at acting cause my little chap living here all normal to him. From breakfast routine to boundaries and smiles etc.

to my daughter I was unwell on Weds after my biopsy I ended up in A&E before I left I burst into tears to my daughter saying I didn’t feel well. I don’t do things like that I don’t cry to her. Bless her she rang my husband her dad saying dad mum really not well come home. So he did. It’s all falling apart I’m falling apart.

why did I turn 50!

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5 Replies
Happyrosie profile image
Happyrosie

LADYT50. Sit down quietly and listen to me.

Maybe you’ve got cancer. What a good thing then that you had a mammogram.

There are thousands of women you’ve been through what you are going through : not your special home circumstances but certainly bad mammograms and then waiting.

That was me over ten years ago.

I AM STILL HERE WELL AND HAPPY.

I had a mastectomy, chemotherapy and radiotherapy which wasn’t pleasant but I AM WELL AND HAPPY.

TEN YEARS LATER.

So will you be.

ks1966 profile image
ks1966

I know this diagnosis is overwhelming, but please remember—breast cancer today is being treated more like a chronic illness than a death sentence. Over the past 10 years, there have been incredible advances in targeted therapies, immunotherapy, and personalized treatment plans that are helping women live longer, fuller lives—even with metastatic disease.

Legsandmore profile image
Legsandmore

As others have said, whilst l know you will be anxious, many of us have faced similar situations and are still here to tell the tale.

I had just turned 50 and life was very good. I had just landed a brilliant new job, was going on the holiday of a lifetime before getting started and l was feeling very fit and healthy.

I got my mammogram appt and my first thought was, l don’t have time for that right now, but that voice of reason told me, you need to go, these checks are important, find the time.

Long story short l had breast cancer in its early stages.

That was in 2009 and despite the cancer having spread to my lymphatic system, much to everyone’s surprise, l am still here to tell the tale.

Please stay positive, l really believe that a positive mental attitude takes you a long way in dealing with this disease.

I wish you all the best and please remember that you are not alone.

GLRocc profile image
GLRocc

What a lot to have to cope with and you must be overwhelmed. As the other posts say try and stay positive, it can be treated and with a good outcome. I had a mastectomy which was far less traumatic than I was expecting, I was up and about the following day and had very little pain. For various reasons I could not have radiotherapy or chemotherapy but I have been on anastrazole which I have coped well with, and I will soon start on a targeted cancer drug which I was dreading, but I found a Breast Cancer Now forum with people on the same drug who are coping well so I now feel better about things. My neighbour had radiotherapy and it wasn't too bad. Macmillan and Breast Cancer Now offer really good practical and emotional support and someone you can talk to, so my advice would be to give them and talk to a specialist nurse or support worker - they really are a huge help. Wishing you all the best

ba5083 profile image
ba5083

When my wife was diagnosed everything was different, driving to work, grocery shopping, sporting events...everything. I had been down this road before with 2 sisters. One didn't end well and passed at 49. If you are open to any advise that helped us and provided some peace. Do your own research. Reading "How to Starve Cancer" provided a lot of peace. It was something I wish we would have done before starting treatments which included double mastectomy, lymph node clearance on 1 side, Chemo and Radiation that my wife is still feeling the affects 3 years later. I wish we would have taken a deep breath and gathered more information prior to jumping right in. I felt we were pressed to make treatment decisions out of fear.

The other recommendation would be to get your vitamin D check. Most DRs don't think it is necessary yet 92% of newly diagnosed BC patients are deficient on Vitamin D. 80% extremely deficient. Get your body to operate in the most efficient state as possible. Your best outcome with the lest amount of side effects depends on it. We are constantly listening to pod casts, watching YouTube videos and researching gut and metabolic health.

My wife is ER+/PR+ (estrogen/progesterone positive) HER2- with ILC (invasive lobular carcinoma).

I watched this video last week which is very encouraging. (it is about an hour+ long and is not political in any way) youtu.be/mgZaT-OriO8?si=Z8n...

There have been a lot of advancements in BC treatments over that past 5 years. PLEASE do your best to take a deep breath. Stress can make things, God Bless!

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