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Does anyone know why some gave lumpectomy before chemo and some after? Apart from the tamoxifen Shirls is same as me but I'm not having lumpectomy till after chemo. Just curious

Anyone got any experience of losing their hair while on Tamoxifen? Went through all treatments last year & got a lovely head of curls back post treatment. In the last week I've lost lots of hair in patches, from the back of my head only (thank God). My GP says Alopecia due to stress. After recent very successful re-con I think I relaxed for the first time since I was diagnosis & that's when the hair loss began. I am no longer losing hair but have bald patches at the back of my head. Luckily I can cover over with other hair at the moment. Am on Tamoxifen since July2011. Anyone any experiences or advice?

I found out in last week that I need to undergo a mastectomy and will be having it in next few weeks. I was hoping to hear from those who have had reconstruction and how you found the recovery and most of all the end result. I would also love to hear about those who did not opt for the reconstruction and decided to have breast prosthesis instead. Have to admit that I am somewhat put off by the surgery time, recovery time of a reconstruction and also the risk that it may fail. Feel it is a big decision and would love to hear from any of you. Many thanks

I had 25 rounds of radiotherapy, finished it on Oct. 1st. I am still completely wiped out after it. Is this normal? I have energy in the morning but then all of a sudden my energy just goes, as if I've just run out of power. A lie down for half an hour recharges me. I go for a walk most days, eat well and get plenty of sleep. When am I going to feel normal again?

hi my name is marion i have finished "ippi" drug 3 mths now .(i had the 4 doses sailed through it tg.) my scan 4 wks after finishing drug it showed no new tumors on my lungs or liver but there are 3 tumors in lungs showing slight increase since may! will have scan in dec and back to dr in jan to see how those tumors are doing this is where i am realy frightened ,i have not spoken to any one with this cancer or who where on this drug or on it now,so i realy would like some suport and advice a bout this cancer .checking the web freeks me out so much negitive info i feel very well and very strong so any help i would be very greatful thanks.

Hi all Just wondering if anyone stayed in the lodge in st Luke's? It's being offered to me as I have to travel a long distance everyday for radiotherapy which is starting tomorrow in st. james hosp. On one hand, I'd like to save myself the hassle of travelling and conserve some energy but on the other hand I'm worried about being away from the kids. I'm also thinking would it make the days very long and lonely. Has anyone stayed there? Any thoughts?

hi everyone. I hope everyone is well and best of luck with rads chemo etc.... I'm still here:-( drains are still pulling too much fluid , but i may get home today.... So five days on, still adjusting to the newness of it all, and just really lookingforward to getting home.... just very afraid of the coming chemo - wish i didnt have to do it

Hi There, Was just wondering if anyone is using Modified Citrus Pectin as a supplement to prostrate cancer medication.My father was diagnosed back in feb 2011 and I have read some interesting articles on its use (Life Extension Magazine March 2009 ).Of course,we will say it to our doctor tomorrow before any decision is made but was just wondering if there are patients using this supplement already, and how they managed to obtain it in Ireland as seems to be only available in USA and Amazon also will not ship it to ireland. Thanking you for any help.

Hi all Well its only taken a year but the penny has dropped well the whole money jar actually!!!I HAD CANCER.Arrrrrgggh!!i finished herceptin last thursday and what a memorable one it was 6 attempts to get vein.Then woke up saturday with cystitus which is now full blown kidney infection.Thought id be sooo happy to be finished but its the strangest feeling.Dont take me wrong i am happy just dont know if im coming or going.I have follow up on monday i assume to check all is well and for the last two weeks or so ive had pain and dull ache in armpit on and off ,dont know if its head playing tricks,scars or the unmentionable!!(had this before diagnoses too)Just have to mention it on monday although i dont want too.This cancer crap is really head wrecking. Hope your all getting on ok xx

Hi gang! Tomorrow we go up to find out what the surgeon and his team found as a result of my mastectomy and auxiliary clearance on nov 15th. Does this vary greatly from the original diagnosis??? Am so afraid that there are still some nasty surprises waiting fir us still on the journey.... My nurse tells me I'm "cancer free" but still won't or can't believe it until I hear it from mr surgeon!! Also my drain is still pulling loads of fluid from my armpit.....it's always very slow in the morning, but when I get up and move around it drains and drains......was hoping to get rid tomorrow but don't think it's likely now......