I like to come on here, this day every year to give a bit of light to those recently diagnosed. I hope others will add to this thread about successful outcomes! And others just diagnosed will feel free to ask questions,
I was diagnosed 3 years ago today and have made a full recovery. I continue to take tamoxifen and get a bit more fatigued when work gets stressful than I used too with a bit of pain in my ribs due to radiotherapy damage but nothing that’s not manageable.
Yes I still worry about every ache and pain, but I’m well and cancer free.
So if you have been recently diagnosed or are going through treatment, try to remember the success rate for treating breast cancer is very high and whilst you are on a terrible roller coaster at the moment, you will come through it and be proud you did. Go with what every emotion is right for you, talk to people and ask for help. But above all, trust the amazing NHS and the staff who know what they are doing and will do their very best to get you through this.
Edit…Today, I’ve just had my third clear mammogram. 3rd January 2024 today is another great day
sending love and hugs x
I was diagnosed around September 2023 and it all started from an ordinary mamagram call up. By the end of October I had my surgery and was so relieved. Until they got the results from the biopsy of another part of my breast. Which was positive and apparently this is unusual. So my new year started with my 1st round of chemo. I'm still not fully understanding or making sense of any of this. I'm trying to be positive and apart from a few close friends and minimal family nobody knows.
Hi Nik Nik
I was diagnosed Nov from my first routine mammogram, surgery just before Xmas and waiting for oncology appointment / chemo dates.
I try to be positive too but it’s easier said than done when you’re caught up in the whirlwind of appointments after diagnosis. Lack of sleep makes it hard - just a couple of hours some nights.
I have told everyone as personally find it easier but we are all different.
Wishing you well xx
I’m sorry you find yourself here. Looking back I really wish I had taken more time to really get better. It is highly emotional and being amongst kids is not always the best way to recover. There aren’t many benefits of teaching at the moment, but sick leave is generous. Take it!
You should take off all the time you need. I'm a retired teacher, and I remember how much commitment and energy is needed, even when you're well. I hope you feel better soon. x
I needed to read this. I am 4 weeks post WLE with some reconfiguration done for Tubular BC and am really struggling with not going back to work until the summer term at the earliest. I am still pretty bruised and have a hematoma. I still get tired very quickly and even light gardening causes pain so I am trying to just listen to my body. Have approximately 4 weeks to wait for oncology to discuss radiotherapy and hormone therapy so could be longer.
I was diagnosed 3 years ago during covid, triple positive, mastectomy, total lymph node removal, chemotherapy 6 treatments of chemo, phesgo , 18 injections, literally 15 minute job, and now biphosphonate infusions twice a year, half hour job. Should finish my treatments in November .Anastrazole tabs for ten years, one little tab every night, no biggy. You just get into the swing of things, becomes a way of life for a couple of years but that’s nothing to what you have to look forward to after
You soon get into the swing and the nurses become friends. I was told by consultant I’ve got a good ten years plus, older you get your risk goes down, I’m 64.
I had my third yearly mammogram 2 weeks ago so
Whatever cancer throws your way, we’re right there with you.
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