I know Candie, I don't like the word "mastectomy" either. It sounds so brutal doesn't it. I think it could be renamed with something prettier but it would still turn the pretty word ugly. Hope all goes well for you and keep posting on here if you need to ask anything or just want to freak out in general. Once you have your treatment plan in place you can join the 'going through treatment' threads and chat with others having the same treatment at the same time. I found this really helpful and have met some of these friends in real life recently. xx
Hi Mai7- thank you for your message and the link to your story. I was told Mastectomy only option due to 3 lessions although small the largest one was invasive the othe 2 in situ about 4 cm apart so covering a large area of the breast, there is also a large area of calcium and also calcium present in one of the lessions. They also think the calcium is promoting the cancer and feel there are other lession under or behind the calcium. i did look at the scan with them and it is spread over the breast, but it was just a shock to hear that word mastectomy as during alll my prev scas and biopsy i was told Oh only small around 4mm the biggest and they could not be felt - it was picked up by a mamaogram.
This forum is brilliant keep up all the brill work ladies you are a good help to us new ladies xxx
Hi, Candie. I've had a double MX (left side out of choice), but I was able to have immediate reconstruction (DIEP flap) 5weeks ago. I had 2 invasive areas grade 1and 2 and a large area if DCIS. Despite this large area they still talked about a therapeutic mamoplasty (breast reduction) I was 38 DD, but they wouldn't do anything straight away about the other side. I knew I didn't want to be lopsided and I knew I didn't want to be flat. I did my research and found out about all the options, did my pros and cons list and made my choice. I know I was in a lucky position with my diagnosis to have a choice and I can't tell you how pleased I am with that choice.
Make sure they have given you all the options and explained why you "have" to have the mastectomy. xxx
Hi Candie, sorry you find yourself here. I had mx and full lymph removal in November and have to wait a year for reconstruction due to my high risk for recurrence. I'm surprised it's an mx for you with grade 1 tumour and no lymph spread. Are you BRACA or is it a large tumour? I can't say it's easy because it really is a horrid thing for a women to have to go through so give yourself time to weep if you need to. I cried every day in the week or two before my surgery. It does get easier. I'm all healed now and getting on with life, pretty normally. Here's my story which you may find some comfort from: http://lifeafterlola.blogspot.com/
Sendng hugs. Xxxx
It's Emily here from Breast Cancer Care.
I'm really sorry to hear about your diagnosis and the shock of finding out you're having a mastectomy so soon. Many of our volunters have had a mastectomy (with a similar diagnosis to you) and would be be happy to talk to you before your surgery if you want to speak to someone who's been there.
If you think this would help while you're waiting for replies on here, feel free to send me a direct message with your name and number, and we'll get in touch to arrange a time for a volunteer to call you.
Wishing you all the best,