Going flat with pride
When diagnosed with early HER2+ DCIS in August (right breast), my decision was immediate. Bilateral mastectomy for me. No reconstruction. Why? I'm 61 years old, have been married twice and have had another 15 year relationship. I'm not looking for a man and furthermore, I don't care whether a man would find my flat chest attractive or not! :) Another factor was the many stories I've read here and elsewhere regarding multiple surgeries and failed reconstructions. Not for me. I also didn't want to throw radiation into the mix of treatments. On the 18th August I underwent the surgery, with no problems. Testing of the removed breasts found another tumour in the left breast, which made my bilateral decision a good one. Four weeks later I began chemotherapy through a port in the chest (Taxol, Herceptin) and finished the Taxol yesterday (YAY for me!). :) I've stuck to my exercise regime throughout and have been able to keep working. To date I have only missed two days of work (touch-wood) which were post surgery, but only because I could do so from home. Brain fog has been probably the biggest issue, due to the level of concentration needed for work. Modafinil has helped with that. I purchased the Medicare-funded prosthesis, but haven't worn them so far. My go-to breasts for everyday are seamless, padded crop tops that you can get in any department store for around $15.00. They are light and comfortable, but I wish they came in natural fibres. In the future I will need to navigate the whole anti-estrogen hormone thing. Hmm. I have a long red scar across my chest, but I don't feel like it's unsightly. I'm bald, but that's temporary. I feel like I'm in a good place. :)
Paclitaxel Delayed
I was supposed to have my 9th paclitaxel this morning but was cancelled because I have had significant increase in numbness in my hands and some pain in my thumb over the past week,(even after onc reduced last weeks dose by 10%) My feet seem fine at the moment. My regular onc was on leave so the one on duty made that decision and said that they will see how I am next week and decide what is next. I am quite disappointed as I was getting towards the end of the chemo and want to get it over and done with. On the other hand I didn’t want to say everything was ok as I had read on a few threads here of the lasting damage PN can do. Has anyone had a similar experience?
Effects of taxol.
I am 79 years old with triple negative. I had a mastectomy and have completed the 12 AC treatment. I am now on week 7 of taxol and have a few issues. Apart from the diarrhoea, beginnings of neuropathy, skin rash, loss of taste I find I have just about lost my voice. Very hoarse and croaky. Is this a normal effect? Has anyone else had this and what can you do.
