Hi Looplinds,
So sorry you are at the begining of the journey, but take heart...I started mine 3 year ago ..and still here caising trouble! I knew exactly what my treatment plan was before it even began. Neo Adjuvent it is called, Chemo - Surgery ( Double MX with tissue expanders) - Radiotherapy. I was fine throughout it all...only now it is hitting me. Did they take any lymph nodes? What kind of cancer is it? I am surprised they have not told you in advance what your treatment plan is...I thought that was the NICE Guidlelines. seems to differ around the country! Not everyone needs Chemo & Rads...some don't need either. All I would advise is ask Onc why they have decided whatever they decide. If you understand more I think it is less frightening in a way...it puts you in a bit of control. Remember this is happening to YOU, not the Doctors surgeons etc. There is a lot of information out there...and a lot of misinformation. It all gets thrown at you so quickly. It is a surreal feeling, but you will get through it. x
Im 58, WLE and SNB 4 weeks ago, I saw the oncologist last week and am going to radiotherapy planning on Monday, to start radiotherapy for 3 weeks after Easter. I just want to get going now. Am pretty scared after reading side effects but the alternative is worse. Got to make up my mind which tablets I want to take this weekend tamoxifen, letrozole or a combination of both. I feel I have come so far already without collapsing into a gibbering wreck, so still looking onwards and upwards and I'm sure you will too xxxx
I remember being in this position three years ago. I found my breast cancer by routine mamogram - I am also 60.
About a week after lumpectomy I saw the breast cancer surgeon, who told me what type of cancer it was, and that he had referred me to an Oncologist for treatment. The appointment came in a few weeks. My husband and daughter came with me, as it can be very difficult to take in all the information. They told me the options and the best course of treatment. Although I was very scared, I felt I was in good hands. I started chemo soon after, and then radiotherapy. Not everyone requires chemo but I had cancer in my lymp nodes, so this was the best course of treatment.
I am now fine and working full time again.
Any more information please post on this site.
Take care xxx
I had no trouble with radiotherapy, a slightly red breast but nothing else. I did feel tired at this time but I had just finished chemo. After the planning appointment and tatoos which were markers, each following appointment lasted about 10/15 mins. sometimes I was in longer if I had to wait. I drove to my appointments and went shopping after. I needed 3 weeks radiotherapy and 1 week booster. There was no pain or sickness. I am on tamoxifen for 5 years, which I have completed 2 years. The side effects are not too bad for me now, the doctor helped me sort the hot flushes. I thought I would gain weight, but I have actually lost 2 1/2 stone I put on during chemo with healthy eating plan.
Life is good now, running after my grandchildren and working full time.
Take care xxx