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Moving forward?


Re: Moving forward?

Hello Owl lady

I'm like you - diagnosed end November 2016 and surgery December 2016 - WLE then rads. I've recently had my 2nd mammo and it was clear, but you're right - the anniversary certainly brings uncomfortable thoughts up, but with a clear result I can put it to the back of the mind for another year.

I do hope it is the same for you. 

As you say, not the best time of year for getting the diagnosis - everyone else all cheerful-seeming when we'd just had bad news. I'm sure as the years go by the fear of recurrence will recede a bit. I tell myself that I am lucky to have an annual mammogram so anything untoward will be picked up at a very  early stage, unlike others my age - 60s - who only get checked every three years. 

I'm also aware that there are worse things than breast cancer that I could have had, things less easily treated, so I aim for the gratitude approach, but we are bound to wobble a bit from time to time. 


Best wishes for tomorrow and have the best Christmas you can. X

Owl lady

Re: Moving forward?

I go for my 2nd mammogram tomorrow, the 2nd one since I was diagnosed Dec 2016. I only have a mammogram on my left side as I had a mastectomy  on the right, the only check on this side is me checking myself which I find difficult with an implant and scars.I find it really hard waiting for the results, which if I'm lucky will arrive just before Christmas. Not a good time of year for me. If there is a problem I will have to wait until the New Year. The mammogram is my only follow up I would find it more reassuring to see the oncoligst once a year also. I tell myself worrying will not change the result. The emotional and mental part is definately harder than the treatment. I know I need to be more positive and live my life, but especially at This time of year I struggle. I hope you all have the best Christmas you can ,those in treatment and those who have finished.


Re: Moving forward?

I dont believe it


What a lovely positive, honest post, thank you so much for that as it will help so many ladies on here to see that it is possible to move forward, albeit that it might take a bit of time, and that there is life after bc treatment.


I am now two years post surgery, one mammogram post surgery, and nearly two years from the end of my active treatment.  Life has returned to normal for me, am on tamoxifen as well and similarily the SEs have not caused me too many problems.


Helena xxx

I dont believe it.

Re: Moving forward?

Hi. I am moving forward too. This is the first week I have not felt a threat of cancer returning. I had my first mammogram one year on from my surgery and treatment and getting good news that all is clear has left me feeling very positive about the future.

I have had a good year and am very grateful that I have a good happy life. I have been on Tamoxifen for a year now and had some SE that came and then went, nothing that I could not live with. I have had two appointments with my oncologist when she examined me and all was clear but it has taken the mammogram to convince me that there is nothing lurking there. I got to see my consultant at the mammogram so he has told me just to go home and get on with life and he will see me next year. We had a joke and he said being from Central Scotland I am probably more at risk from stroke or heart attack. No comfort from those horrible options but reassuring regarding cancer. Just be aware was his advice.

The breast that had the surgery/treatment has had some niggles, some aches and pains and most mornings has many indents on it from the creases on the quilt. My BC. Nurse tells me all of these are common. The nipple and the area around it has a mind of its own. Changes shape and colour sometimes but again just normal effect from radiotherapy. I am just getting used to it being this way and is a small price to pay considering what was there.

For all of you who are just setting of on this horrible journey I wish you all well. It's never a good time but I found it especially hard at Christmas time. The hardest part for me was the mental and emotional part of it all and the waiting was a nightmare. Because of my personal circumstances only my husband knew about it initally and then I eventually told my daughter and then my sister.

As some time had passed and I was already through surgery I decided not to spoil other family and friends Christmas so I told know one else. I have never told anyone since and this has helped me as everyone is still normal with me. I am sure everyone will have their own way with dealing with it but I have found it good not to have to deal with it daily or in every conversation with friends or family. I find I am reminded enough with the coverage on television or mail through the door. It will be very helpful though for people who need a good support network to talk about it and try and get some true friends and family to be there for you.

I drop in to the Forum every few weeks or so when I have time and it's heart breaking to see and read of all the journeys that people are going through. I know in the beginning I was just at such a loss as to what was happening to me and imagining what scenarios I could possibly face. I just appreciate now that treatment has advanced so much and the outcomes are more favourable. 

I have decided now to live life to the full. I will take my consultants advice and be breast aware but I won't let it rule my every thought. 

It has taken a year to find this emotional strength again and I am so positive about the future.  I hope with time everyone will find some peace with their situation and be able to enjoy life once more.  Xxxxxxx












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Re: Moving forward?



Pleased to hear you found the Forum helpful. Hopefully other Forum users will reply soon. If you'd like to talk things through at any point as you move forward from the hospital based treatment, please phone our free Helpline on 0808 800 6000.


Best wishes



Moving forward?

Tomorrow I am going to the oncologist for what I think is my final appointment. I was diagnosed in April, op for DCIS and lymph removal in May, radiotherapy through August. I’ve creamed everyday with Aveeno, drunk lots of water, eaten lots of nuts and fruits. I’ve had breast ‘cramps’ and painful arm when I lift anything slightly heavy. No skin problems at all. I never got a sense of ‘team’ through my treatment- different people daily- all nice and efficient, but didn’t feel a great deal of being cared for. I have really benefited from this forum- thank you everyone.