Thank you so much for your message, it has made me feel so much better as I'm going for a Radiologist appt today to check out the lymph nodes and am terrified! Surgery is scheduled for the 21st and I've been reading her the "Mummy's Lump" book, she really likes it and asks for it every night, I then ask her if she has questions about my lump and she often has 2 or 3 and then goes to sleep quite happy! If you don't mind me asking, how long did your treatment take? I'm less than a year in my new job and want to set expectations with them about how long I will be off..Thanks, Helen xx
Hi Helen, my daughter was 4 when i was diagnosed 3 years ago. We told her that mummy had a poorly boobie and needed an operation, she was happy with that. When my treatment plan included chemo we told her that I needed some medicine to make me better but it would make my hair fall out and might make me feel poorly, we stressed that it was only the medicine i was having that caused this and nothing that she ever had to take would. She accepted everything we told her and never really questioned it, we also spoke to the school who were brilliant with us. I struggled with the thought that everyone knew what I was going through and found it hard to be amongst people with nobody daring to mention the fact that i was bald, i was also paranoid about taking my daughter into school with all those little darlings full of snot and lurgy, so the headmisstress allowed me to take her to school a few minutes late and the office staff took her to her classroom. Hope this helps, please feel free to PM me, take care CC x
Xx I also told the adults around me that my girls didnt want to discuss it with anyone, as they said so, and have tried to control the hysterical types who get overdramatic.
Thanks so much for your message, that really helps. I agree, being honest with her is important and she has been really gentle... it's amazing how much small children pick up on so I want to make sure that she has the opportunity to ask whatever questions she wants to xx
Thanks Janet, they are really helpful xx
Hi helen, my girls are 10 and 11, so thats a big differance.
However one of mine asked me in the car on the way to school if I had cancer. (Car swerved a little)
I said it was a complicated story, as I was pre definate diagnosis then, anyway.
How I explained it to them was that I had a hard lump in my breast. (Which they both asked to see )mine was 5cm so it was easy to feel.
I said that sometimes your body goes a bit silly and makes a lump that doesnt know when to stop growing, so theres not enough room for it, a doctor has to take it out in hospital and sometimes you end up needing horrible medicine that makes you feel sick to make sure the lump doesnt come back.
Both girls have had a couple of moments of being sad and concerned but seem to be ok with it.
As mine was found at the end of October, breast cancer month, I pointed out that all the money raised from pink ribbons,pens etc went to research, so they know how to fix it.
They insisted on checking out my mastectomy wound, and their biggest concern is if it hurts. I said I have medicine like pamol that means it doesnt.
I believe you need to say something, mine figured it out from overheard snippets, children make stuff up in their heads otherwise.
The other thing is, if they havent dealt with it before a calm explanation is not really scary, they havent watched hideous medical dramas, or seen statistics that terrify us.
They will take their cue from you. And they give the best most gentle hugs xxx
I've attached a link to the BCC publications "Mummy's lump" and "Talking to your children" which you might find helpful:
Very best wishes
That's a really helpful message, I will get in touch with them and get hold of the booklets. My Husband lost his Dad to cancer so I think he's not happy with the word either. I hope your operation goes well and thanks so much for taking the time to reply to me, this forum is proving invaluable to someone waiting for results and recently diagnosed - I really don't feel alone any more!
Thank you, Helen x
I was diagnosed with BC last week and am awaiting the results of my MRI to agree the treatment plan. My four year old daughter has been asking me all about "Mummy's owie" since she saw my biopsy plaster and I really am at a loss as to what to say to her. Should I be honest or pretend that nothing is happening? I want her to understand that things are not right, particularly if the treatment is aggressive and/or if a family member or friend says something to her.
Does anyone have any recent experience and advice? Thanks, Helen xx