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Hi all, I have decided to take part in Dublin mini-marathon on Bank Holiday Monday 7th June to raise money for breast cancer research. If you think you might be able to do it, however slowly, I'd love to get a group of ladies together. If you are interested please send me email to m_ltk@yahoo.co.uk or call me on 087-6642202. Thanks, Michelle

I met a lovely woman at the ARC center in eccles street yesterday. It is a lovely place for people who have cancer to go to. They have relaxation classes, councelling, thi chi, and lots of other stuff going on. It is also a drop in center, where you can go and have a cuppa. They have a fabulous garden aswell. Now im getting to my point...lol There is a meeting there on the 12th of April at 10.15 for young women with breast cancer. Its for anyone up to 45 ish (maybe a bit older ) I think they have it 4 times a year, im so glad i heard about it!!!! I definately want to go, and celine from here said she would be intrested. It would be a great way for us to meet up! So is there anyone else up for it?????

Hi there, I had breast cancer 18 yrs ago at 42 and was diagnosed with a recurrance in 2008, I have both lobular invasive and ductal breast cancer now. I have secondaries in lungs, and bones. I have had Taxotare chemo and continue on Zometa for the bones I have resisted Femara until now but due to lung problems gave it a try but had very bad pain and stopped it anyone out there got any any experience of Femara. Im am almost pain free without it dont know what to do. Mosaic

Hi, Having some physio to strenghten my back after various surgeries & my physio gave me a flyer about this group. For anyone sporty or wishing to learn a new sport the Plurabelle Paddlers is organising training for dragon boat races/canoeing. The exercise programme is specifically for women who have had breast cancer treatment. Suitable for those have finished treatment at least 3 months ago. They have an open day on April 17th 11am-1pm at Waterways Ireland Visitor Centre. More details on www.plurabellepaddlers.com A

Hi Every one, I'm new and nervous. My name is Lou, I'm 41 and married with 3 children in the north east and I am going to the clinic next tuesday in Beaumont. I had a breast uplift and implant in November 08 for personal reasons. I was delighted with this and it really did make an awful difference to my life as it was something I had always been very self concious about. I had this done abroad and was very happy with the level opf care received. The implant in the left breast has always given me a bit of bother in that it seemed to settle high and was a bit harder than the other one.I was worried it may have been a thing called capsular contraction [scar tissue that squeezes and distorts the implantr and can cause pain] .I had this checked by a dr and he sad it was ok and best to leave it. He thought it was too early for capsular contarction to form as the implant had been harder a few weeks after surgery and generaly it takes time for scar tissue to build up. But a few weeks ago I found a lump that wasn't there or that I did not notice before.There actually seems to be a lot of lumpy areas so it is hard to tell what is ne and what is not. I am hoping it is this implant. I am so worried as I have had pain in my scapular area in my back recently too but didn't connect the two. And new stabbing pains in the breast on occaision. I am worried that the Dr's or radiographers might not have the expertise with implants.I'm scared they will miss something or think I'm a nutter for having gone and done this operation the first place.I'm worried because I had my surgery abroad I may not be treated here and told to go back abroad.. I was coping finewith all of this until last night and then it became really scary and overwhelming and i could not stop crying and could not sleep. Now I'm imagining every ache and pain is something dreadful as I have some pain under the breast to the left as if in the chest wall. Could be stress related...I feel my chest is going to explode with nerves and stress and I'm terrified of needles and the tests if I do need them. Any comments or advice you can give would be great . I have read some of your stories and you are all amazing. Thanks a milion for reading. Hope to hear from any of you.you are in mythoughts even tho' I know none of you. Thanks . Lou

Hi, I was diagnosed with Breast Cancer on 6th January (the day of the "big freeze", I'll never forget that date). Had lumpectomy, lymph nodes clear (happy days!) but was devastated to be told, following more tests, that I have bone mets - shoulder, T2 spine, pelvis. Had some radiotherapy to shoulder for pain and I am due to start chemo next Tuesday, 13th April. 4 bi-weekly AC chemo + avastin, another pet scan, break, then 12 x weekly taxol. I am terrified and dreading the chemo, any reassurances and tips for coping with chemo would be welcome. Stella

does anyone know why Castineira's clinics are being canceled and moved to waterford and he is not there either

My son has just been diagnosed with Ewing Sacoma in his pelvis. Surgery is not an option. Chemoterapy & radioterapy are the only treatments. Can I have some advice & has anybody succeeded in making a full recovery or had experience of this condition

I'm just over a year out of treatment and my breathing is terrible, its like I have a tightness in my chest the whole time and struggle to breath properly. Hospital dismiss it and have said nothing is showing up. Anyone else having these symptoms?

Hi does anyone have any information on the Dragon Boat Information meeting on next Saturday - I heard about it but didn't get the details Many thanks