Invasive ductal carcinoma (IDC): Anyone else?
I have rec’d 4 chemo + 16 radiation treatments for invasive. Has lumpectomie 1st....then one week later...
Dissection 17 lymph nodes & 3 tumors removed tumors
Got clean margin.
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There is a thread from a long time ago about this very thing, but my memory is failing me about the title and I can’t find it.
I did tell people a few times that I was “really crappy, but thanks for asking”. Now I can think back at the shocked faces and laugh.
Do you have a treatment plan yet?
Why does every nurse, technician, and doctor smile and ask, "How are you today?"
Obviously they know how I am. I find their inane question very irritating, and usually answer, "I'm probably feeling like every other woman with breast cancer." They really do not understand or really want to know how I feel. Their question is extremely generic and trite, which tells me they really don't think of me as a person.
A breast cancer diagnosis is a traumatic experience! So many emotions are triggered and can linger.
Yes anger, confusion, fear, “why me”? ( why anyone?) … all the above emotions …and more. We all have them and then or despite that, we must move on.
Get a helping hand; someone who asks how are you doing and really wants to hear the answer , someone who can be there when you meet with docs and can “hear” with/for you those hard to hear things. Someone who can read up on stuff that you are afraid to read about . Get all the information you can about your BC and options . It’s a very steep and swift learning curve as so many important decisions will be made in quick order.
Anger will come … and go. Getting the treatment you need will serve you best right now. It does get easier as you move down the treatment path. In fairly short order you will be reassuring others ( I know it’s hard to wrap one’s head around that).
Best to you on the path 🌸
Most people have no idea what a difficult journey breast cancer takes its victims through. Most people think once you have your surgery all has been taken care of and you go back to your normal life. We know differently. My surgery was last year. Then chemo. Then radiation. Then lymphedema. Then occupational therapy. Then side effects of treatment.Not sure what the future holds for me-sometimes I’m sad, sometimes I’m angry, sometimes I don’t recognize myself. Sometimes I want to help someone just starting this unwanted journey. Just know that sometimes I have an absolutely wonderful “normal” day where I laugh, do the things I did before I was diagnosed. It helps to talk, find a recovery group. Visit this site.
Happy for you all. You seem to be coping well. Since my diagnosis, I have been very angry. Just don’t want to see anyone who would ask the usual question when you meet « how are you? » No one wants to hear that you might feel shitty. Haven’t started any treatment since surgery- just want the whole thing to go away but I know it won’t.
You’ve got this! Stay strong 💪🏼 & positive 💓
Love your handle name. 🌲
You are absolutely also forging the way! Thanks for sharing your experience. It is, without a doubt, invaluable for us to hear and know each other’s stories. Peace and all good!
@sequoiatree I also "went flat" and it has worked out really well. Good luck!
You sound strong! Focused! Informed! You go,Girl!! So many have gone before us leaving this wealth of information and inspiration! I hope you have someone who can hold your hand, offer a hug, lend a hand. It is a special strength to ask for help. We are all in this with you.
Wonderful positive attitude. FORGE ON and keep us posted.
Blessings on this path. ☀️