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TAC three completed today!!! Yay!! 3 down- 3 to go!!

Well ladies I have signed up and in training.Two years ago I got the worst news any of us can get Breast Cancer but two years on im trying to keep busy and I love the fresh air so walking is something I love.Having said that I have entered in the Jogging section so I will have to up the pace a small bit. It will be 2 years on 2nd March since my Mastectomy and finished Chemo in July 2011. So for all the NEWBIES I was you 2 years ago and see where I am now keep asking the questions the ladies on hear are fantastic help and support. Claire

Has anyone done there chemo with this on. Was thinking of giving it a try. It's available in tallaght hospital but not Vincent's but jw says she does it in tallaght.

Hi all Will be flying at the end of the month and am concerned about Lymphodema following the axillary clearance. The surgical team say don't wear a compression sleeve just drink water and get up and move around and do arm exercises. Other hospitals say wear the sleeve. Needless to say I don't want to get Lymphodema. Anyone had any experience out there recently with flying. What kind of exercise would help on the flight etc. Thanks D

Hello ladies, another new one for the board. Was diagnosed on Feb 14th, a Valentines Day I'll never forget. Don't know a huge amount yet about the type of cancer I have but what is I do know is that it's grade 2 ductal cancer, estrogen +, herceptin neg. Going for surgery with sentinel node biopsy. No MRI or CT scan at moment until after surgery if deemed needed. I'm attending Waterford. It's so confusing as so many women on here seem to be having all these tests doing first before surgery but my doc seems to want to get surgery done before doing more tests. I realise that there are so many diff types of 'breast cancer' no one fit solution for all. Anyway booked in for mastectomy next Wed March 6th. Not suitable candidate for partial as I have a few lumps when removed will result in basically the top half of my breast going so have decided that losing the entire breast may be less traumatic than waking up and finding just a bit of one left (not that I think waking up without my breast will be anything but traumatic) Meeting my surgeon tomorrow again so I'd like some advise on what questions I should be asking him? I have some questions that I know I def want the answers to but for those of you who are further along this journey than me you may be able to advise me on what I need to know. I'm the type of person who needs to be fully informed. Once I have details I can start to deal with things but don't keep me in the dark. Any and all advise would be really appreciated. Thx.

Hi there, was told today that my cancer is 'occult'. That it couldn't be seen on my mammograms but showed up on the ultrasound. Tumours can also be easily felt through the skin. Seemingly it happens in 10-15% of cancer cases. Anyone else get this diagnosis?

Hi all You might find this interesting. Aine Lawlor was talking to an oncologist about breast cancer treatments this morning. It's listed as "Saving women's lives every day". It mentions new research into a drug for hormone receptor positive tumours. http://www.rte.ie/news/morningireland/player.html

Anyone on herceptin experienced runny nose sinusy type feeling? Just recall someone saying it. I've got it now just wondering is it the herceptin or just me?

Isn't it amazing that my lashes and eyebrows were fine while having chemo and now 8 weeks out of chemo land and I've three lashes on one eye and two on the other eye and the brows are nearly gone. Dies it take long before they start to come back? Hair is good hopefully in another month I can go public!!! All this is not that important just curious. Xxx

I'm just wondering if other people are experiencing long delays in having their disability allowance claims dealt with by the dept of social protection. (have no entitlement to disability benefit as not enough relevant stamps now). I sent mine in after my surgery in Aug.2012 as I didn't even have time to think about things like money when I was hit with a cancer diagnosis. Fast forward and its now over 7 months later and last I was told was maybe April 2013 I might hear something. There are also secondary benefits like support with fuel, travel etc. which I couldn't access this winter as my claim has to be approved first. I'm finding it hard coping with the long delay and feel surely I can't be on my own. The dept says they are dealing with claims by date sent in. Just curious how others finding the system.