Hi Ladies
Had mastectomy last September right hand side and am due to have left mastectomy next month. Anyone in this situation not have Reconstruction done?
Thanks
Dane
Ladies, I desperately need your advice cos no one else understands!! I am 12 months into my cancer treatment, had chemo, surgery, rads and tamoxifen and I have just had enough! I'm done.
I have had severe reactions consistently throughout my treatment and because I was so young I was just told I was stressed out. During chemo at varying stages I lost the ability to speak and walk, my head has been melted from all the drugs and I am just not able to make decisions, or be independent essentially, my head is just so badly fogged from everything. Anyway tamoxifen was suppose to be my last treatment, I was on it and due to severe reactions it was stopped for 6 wks and I felt great, then tried it again and only lasted 4 wks on it and my tremor came back (started with chemo but faded slowly after 6months) so it has now been stopped again. I just can't take it anymore, I seem to be really sensitive to drugs and no matter what, I suffer side effects. I just want to be normal and get back to some sort of life but I can't do that on drugs.
I am going to tell my oncologist I have had enough and am refusing further treatment cos I can't take it anymore. I have had to give up my life for the last yr and am still waiting for final reconstruction in early oct but then I am off to aus to start again.
As far as I am aware the tamoxifen reduces my personal risk of reoccurrence from 15% to 10% which I personally think is useless to me cos if u get cancer in ur 20's there is no way I will get a forty year free pass, if its going to come back it will and I have a tried everything to give myself the best chance but enough is enough!
Ye know the pains associated with all the different medications and know that it's not easyi would like to hear your thought before I make radical decisions, any advice really appreciated!!!!
Hello everyone!
I recently received a beautiful card from a close friend of mine in Oz and I hope you don't mind my sharing it with you .. it read..
[color=#4000FF:1y70ytv7]Be gentle on yourself today..
Lightly blow your cares away..
Honour all the things you're feeling..
For within you lies the path to healing..[/color:1y70ytv7]
Resolute
Hi Ladies
So sorry have not been on for AGES!!!! last time I think I posted was when had finished final chemo. Due mascetomy on Tuesday week in Vinnies.
Just wanted to let you know if any ladies are interested am having a post chemo booze up this Saturday in the Goat Grill in Goatstown will be a good crowd and having a DJ to celebrate getting this far. If any of you around and would like to come please feel free.
I will be back soon to read all new posts life has been hectic!
Dee
XX
Did anyone else have an expander implant fitted when they had their mastectomy and then have a Diep reconstruction later? just wondering how it turned out as I was recommended to have the expander to preserve my skin, but the plastic surgeon says it might make recon more difficult and he would not have recommended it! I was reluctant to have any implant but thought it would give the best end result, now I'm not so sure!
Karen
Hi, I wish to recommend -hopefully I can- ...
[b:dq5w5lu0][edited by webmaster to remove advertising][/b:dq5w5lu0]
I'm just sharing, because it's good think, and I'm really hoping that I'm not breaking any web site rules. I know some place do mind. In this case sorry for that.
[b:dq5w5lu0]From webmaster: [/b:dq5w5lu0] Sorry to edit your post but we can't allow advertising on the message board.
Hi ladies
Just wondering if anyone has had to have their tendon seperated following Latissimus Dorsi reconstruction?
It looks like this is on the cards for me. I blocked my ears when the surgeon started talking about it the other day & told her we might talk about it over a cup of tea in a few months!
But of course now I'm curious and keeping true to myself, I haven't been able to see much about it on the normal, reliable websites.
Anyone been through this?
Hi just wondering if anyone suffered chronic radiation enteritis of the bowel after radiation treatment. I was hoping to share information and discuss this problem with someone experiencing similar side effects - nausea, loss of appetite, pain etc.
I am currently on a lactose free diet and am trying various foods to see what suits my current constitution.
Thanks,
John
Irish Cancer Society Head office, 43/45 Northumberland Road Dublin, D04 VX65; Charity Regulatory Authority No. 20009502; Revenue Number CHY5863; Company Number 20868.