Forum Discussion
Coco65
9 years agoMember
I am in shock
I was diagnosed yesterday 2/06 and I'm feeling a lot of different emotions.
The hardest part is having to tell my kids, all teenagers and one has taken it particularly hard, so whilst I want to just fall apart I am staying strong for them so as not to scare them.
My surgeon tells me it is very early Breast Cancer detected by a Mammogram, I am 52 and married to a wonderful supportive man.
I have no lump and if I had't had the Mammogram I wouldn't have known, I am one of 11 children and 9 of them are girls so that 1 in 8 women statistic has hit the nail on the head.
I am so scared and I joined this group in the hope of getting some much needed support from other women that have been through this.
I am waiting to be booked in for my biopsy and he tells me I will then need surgery to remove it followed by 3-5 weeks of radiation everyday.
The hardest part is having to tell my kids, all teenagers and one has taken it particularly hard, so whilst I want to just fall apart I am staying strong for them so as not to scare them.
My surgeon tells me it is very early Breast Cancer detected by a Mammogram, I am 52 and married to a wonderful supportive man.
I have no lump and if I had't had the Mammogram I wouldn't have known, I am one of 11 children and 9 of them are girls so that 1 in 8 women statistic has hit the nail on the head.
I am so scared and I joined this group in the hope of getting some much needed support from other women that have been through this.
I am waiting to be booked in for my biopsy and he tells me I will then need surgery to remove it followed by 3-5 weeks of radiation everyday.
37 Replies
- Hi @Coco65 welcome, I am very new to this "club" too. Both my sister and I have been diagnosed this year but our journeys are quite different but we can relate to each other. I have 4 daughters and am worried for them. My Mum had bc too. I'm relatively early on in my treatment, had a partial 3 weeks ago, they found another mass that they didn't know was there when the pathology came back, going for an extra excision next week with sentinel node biopsy then if that's clear 5 weeks of radiotherapy. I don't have much advice to give you as I'm quite early in the process myself but you can only take one step at a time and deal with each new situation as it comes along. Good luck and keep talking xxoo
- Coco65Member@SisterofCoco this is supposed to be my no tears day! Love you too you help me to be strong! I am one determined lady!
- socodaMemberHey @SisterofCoco, Suzy. A big welcome to you too. Please know that we are also here for you as well, as it's incredibly hard to watch a loved one go through this. You all sound like an incredibly loving close family and that will help all of you in supporting each other. Wishing you all the best. Big hug. Xx Cath
- SisterofCocoMemberHi everyone , I'm Suzy and #Coco65 is my sister and she is an amazing sister and has raised 3 beautiful boys whom I adore. She is strong and will do whats needed when its needed and keep moving forward. I am so grateful.and happy she found you all . I've read through the comments and know whatever she comes across you guys will help and advise her .... Thank you all so much you have already helped her more than you know . While Jojo's diagnosis has rattled us all as as she said we are 9 girls 2 boys and until now BC free and I know this will empower us all and we shall move forward with more knowlege and awareness .... This isn't my first experience with BC having very close friends whom I have had very close contact with all the highs and lows of this disease but when its your sister ....its on another level .... and I will be there for her as needed and I know here you all will be as well ...Jojo has jumped up and got herself ready for this fight and I couldn't be prouder of her . #fightlikemysister #yougotthis #iloveyou xo
- adeanMemberWelcome l wanted to next week for me it will be 5 years since l was diagnosed and its like yesterday. This is an experience like no other but you get through it emotionaly physicaly and mentally but it changes you and l love the new me. Yes good days bad days better days. Welcome adean xxx
- Michelle49MemberHi coco
I'll start by saying sorry you have to be here but now that you are take a breath, I am 18 days post mastectomy. I found a lump after I received a sharp pain in my right breast on 23rd April , 24 th biopsy, 2nd may meeting with breast surgeon, 3rd ct and bone scan, 9th back to surgeon, 16 more tests , 17th mastectomy, 18th another surgery due to a haematoma in my chest and back home on the 20. That has been my journey so far.
With that said it is hard to get the news that you have breast cancer, it's scary! . Take each step at a time, just say to your self " right I'm here my next step is a biopsy " don't try and look into the future and think what if? That has been the best advise that I have gotten from the wonderful women on this site .
The other advice that I have gotten and will give to you is , be selfish let people know when you don't want to talk and when you do,when to visit and when to leave you alone, take the time for you and your family to process each bit of information you are given and remember each and every women on this site will be there for you any time you need advice or an ear for you to voice your concerns.
Best wishes and keep breathing deep calming breaths you are not alone ❤️❤️❤️❤️ - melclarityMemberSee Jo!? I love what @Nikkid did, and it was perfectly OK to do that! so its great hearing the different approaches! helps ease your mind too that waiting is absolutely fine. x M
- Coco65Member@nikkid thank you! That puts it in perspective. xx
- Coco65Member@melclarity
Thank you! You really have helped me today - nikkidMember@Coco65 when I was diagnosed my first question to the surgeon was 'can I have 10 weeks before we operate'? There were lots of things I had to do (I have my own business) and commitments I had in place. Because it was early and the biopsy indicated it was slow growing, the surgeon agreed - and I was put on Tamoxifen in the meantime. This gave me 'mind space', time to research (I got a second opinion just for peace of mind) and the ability to get myself back in control. The surgeon actually said to me during one visit "I get it Nikki, YOU have to get in control of this cancer." So I had time. Of course, if the surgeon had said 'no" because it was aggressive or dangerous to wait, I would've done what I was told.
I'm just telling you this because there isn't always a need to rush in. Everyone is different, everyone's cancer is different - but in my case, I needed the time and don't regret it at all.
So 1.5 weeks may not be a problem for you seeing as it's so early xxxxx