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I've posted a few comments under topics started by others. I love the fact that I can read the comments and relate to them. But I'm just wondering if anyone else feels as I do. I attend all my appointments, deal with any pain I have but I still feel that this is happening to someone else. If I had to tell someone the date I was diagnosed or had my lumpectomy I would have to look it up on the calender. Its as if I'm blocking all this out of my mind. After the initial shock its as if its not happening. Maybe its a good way to deal with it but I'm kinda afraid that it will hit me some time soon.

Hi girls, can't sleep. Such a big discussion to make by next Friday. Going to my own Dr for advice on Monday, but would love to hear some advice from my breast cancer friends. Went to see my oncology Dr last Friday. Lovely Dr he talked about my treatments and gave me lots of %. I think the final outcomwins to be made by me. Anyway it goes like this hormone benefit 6.6 without relapse in 10 years, chemo 6.5.without relapse ,combined therapy 10.6 without relapse. They feel the hormone treatment will be enough as the difference is only 4 %, I want to best treatment to stop cancer returning, so I keep thinking gosh 4 % is still 4% better off. As I am otherwise healthy, so what if I feel pure crap for 6 months in order to live longer. I would walk on hot coals in order to live longer. Would love to hear what others think. Well must try to get some sleep. Night all. G x

Anyone know where I can buy a compression sleeve for flying? Six months on from surgery, I still have a touch of lymphodoema and someone said I should wear one of these when I fly to Portugal. I've seen stockings in chemists, do they do ones for arms too?? I don't have time to source one online really as we go Monday. thanks in advance.

Hi all 2 chemo yest and wasn't as bad. Firstly I took 1/2 a sleeping tablet in the morning, then I managed a litre of water by the time it was time to go in and I wore extra clothes and had a fleece jacket wrapped around my arm to keep it warm. And hey presto, my veins showed themselves this time!! The after effects ok so far. Did have some nausea but the new tablets seem to have held it at bay. Also, I took sleeping tablet last night so slept through whatever going on People who know me would be amazed I took sleeping tabs, I'm the healthy freak, when I'm anywhere new I do tours of health food shops, and won't even take a paracetamol for a headache. Well, I've decide now, it's time to fight fire with fire! Good luck to all on chemo. Josephine

Hi all Is anyone else on this trial? I'm due to get 1st injection today. I couldn't face it on day of chemo on wed. I feel so ick today I don't feel like it either. I'm told I'm the last person into the trial. Hard to make decisions about these things. I'm afraid to be in and I'm afraid to be out of trial. Anyone any thoughts Josephine

Afternoon all, Only lasted 5 out of 6 chemos. Should have had the last one today but they decided not to go ahead. Have been on Taxol and Clycocystamide on a 3 weekly cycle. Questions for all you ladies who have been through and finished chemo.... How long before your hair starts to grow back? How long before chemo brain passes? (feeling stupider by the minute:-)) How long do you still have chemo symptoms for? Had reimaging done last Friday and will have all the results on the 10th. Anxious as to how the chemo has worked. It has certainly given me the side effects .... lol ..... but has it actually affected either of the 2 types of cancer I have remains to be seen. Surgery set for Sept - just waiting on the date now. Still absolutely hate, hate, hate the thought of it. Any tips from anyone who has been through it without immediate reconstruction gratefully received. Thanks to all Dane

Hi All, Sorry if I'm starting a thread that's already been discussed on here. I'm at my wits end with this whole menopause lark!! I know I need to do more research myself but I said I'd ask for a little advice from you guys first. I finished my TCH x 6 on June 6th. I'll be getting Herceptin until Feb 2013. I also finished 18 sessions of RT on July 27th. (Exhausted!!). I stopped having periods immediately after starting chemo on 22nd Feb, so I did start having a few hot flushes back then. But holy God almighty above in heaven this Tamoxifen lark is no joke at all. I'm crucified from the hot flushes and night sweats. Actually I don't really mind the hot flushes during the day it's the ones when I'm in bed that bother me the most. I'm triple positive so obviously I can't take anything hormone-related, or simulated to ease my symptoms. Does anyone have any helpful hints or tips that might help me through these few months? Also, I'll only be 42 when I finish taking the tamoxifen, and there's a possibility that I'll come back out of this chemical menopause, but I really really don't ever want to have to go through this again. What are my choices? Sarah. XXX

WOULD LIKE TO HEAR FROM ANY ONE OUT THERE WHO IS DIABETIC ON INSULIN AND HAS BEEN TREATED FOR BREAST CANCER. I HAD LUMP REMOVED.. RADIOTHERAPY.. AND A YEAR ON HERCEPTIN I DID NOT HAVE CHEMOTHERAPY DUE TO OTHER HEALTH PROBLEMS MY EMAIL IS : glucosesweet2002@yahoo.com smiles are because i am in remission and also because I have remained positive through out

Hi all Just wondering how long it took for people's hair to grow back? I finished chemo last october and had radio in January and February finished herceptin in June. While the hair on my body has come back with a vengeance the hair on my head has remained very sparse. I am beginning to worry if it will ever grow back. Would like to know how others have got on. Thanks Madge

Hi, I had a mastectomy and reconstruction on my left side six years ago. I am now pregnant with twins (thought it would never happen) and my issue is that my right breast has increased in size and I need advise on what to buy and where to buy it for the other side to make them match!