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Hi I went to my gp today after finding a lump in my armpit about 4 or 5 weeks ago. It’s painless but yesterday and today I have a tingling sensation going down my arm to my fingers which is annoying only. I checked my own breasts and didn’t feel anything but Iv naturally lumpy breasts. Gp checked breasts couldn’t find anything either but has referred me to have a mammogram and ultrasound for the lump under my arm as it visibly noticeable with arm lifted but also while looking at me straight on in a sitting position . She said she doesn’t think it’s anything to worry about but better to get it checked out and said I could be called anywhere between 2 to 4 weeks. I’m 44yrs old and 4 months post vaginal hysterectomy due to fibroids and prolapse womb and bladder on hrt 4 yrs as went into early menopause. I feel well in myself but tiredness is my biggest issue. Iv two daughters early teens , husband and my mind is on over drive with if buts and maybes. has anyone been diagnosed with under arm lump or had an under arm lump and it turned out to be ok? Sorry for the rant and TIA

I had prostate cancer some years ago. And it was successfully treated by brachytherapy. Unfortunately it has returned. My consultant has now recommended testosterone suppressing medication followed by focussed, high-dose brachytherapy. There are risks of damaging side effects with this treatment. I am aware of newer, reportedly much less risky treatments abroad such as NanoKnife ( irreversible electroporation ) in the UK ( London)and elsewhere. This is not available here. Anybody out there willing to share their NanoKnife experience with me please?

So I Finally got called for my mammograms and ultrasound over 3 months after 1st breast clinic appointment. I ended up having biopsies on the lump and a lymph node. Breast changes just keep coming :( lump increasing, skin dimpling and puckering, change in texture, unexplained cording and swollen lymph nodes… I was told I’d be called back in 2 weeks for results. I got appointment letter 3 days later but doesn’t mention to bring anyone. Is this a good sign do you think or was it just an automated appointment and a standard letter sent…. Can reports be done and discussed so quickly, in 3 days? Trying to stay positive 🙏🏼

Lung cancer is one of the most common cancers in Ireland. Early detection of lung cancer does improve survival. If you have any symptoms of lung cancer it is important that you get these reviewed by your GP. Symptoms of lung cancer include:A cough that doesn’t go away, or a change in a long-term coughWheezing, difficulty breathing or shortness of breathRepeated chest infections that won’t go away, even after antibioticsCoughing up blood-stained phlegm (sputum)Pain in your chest, especially when you cough or breathe inDifficulty swallowingUnexplained weight loss/ appetite lossIf you have any of these symptoms it is important to have them reviewed by your GP. After reviewing you, your GP may recommend that you are referred to a Rapid Access Lung Clinic for further investigations. Rapid access clinics provide initial investigations for those with suspected lung cancer and help reduce the time waiting for investigations and a diagnosis. You can contact our nurses on the Support Line if you have any questions or would like information about supports available. Our Support Line number is 1800 200 700, Monday – Friday, 9am – 5pm. 

Hi my husband was diagnosed with testicular cancer in august, tumour removed and all was fine until we received a call to say they think he may have it in his nodes. he’s due to have a EUS and petscan, we have limited VHI cover, will we have to pay a % of the petscan or is this 100% covered under the HSE . i’m worried about finances as he will be out of work once the treatment starts . Ger

Hi, I have been having issues with stomach pains for over a year know. Had a colonscopy. Endoscopy. Capsule endosocpy ultrasounds ct scans. Only thing found was gastritis. My dad had pa creation cancer in 2015 and my pain is on a daily basis with fatigue. I am really scared that something was missed but I feel like my doctor is not listening to my co concerns I have 2 small kids and I fear it might be cancer but feel like I am not been taken seriously.

Having been diagnosed with prostate cancer in February this year at the grand old age of 40, I had surgery in June. Cancer has officially gone, but its the after effects of surgery I'm struggling with. No more than the lack of elections, using the pump once a day for 10 minutes, have been a bit slack this week, only used it 3 times. The viagra isn't having any effect whatsoever, going from a walking erection to nothing is difficult mentally. To be honest the urge isn't even there anymore. I have full control of the bladder and use the gym around 3 to 4 times a week, I'm in pretty good shape physically considering what I went through, just this last hurdle to get over. I know it can take anything up to 2 years to get back to near where I was previously, I just suppose I needed to vent a little is all

Hi folks. I'm 53. I was diagnosed with Prostate Cancer on 16th October 2023. Gleason 7 (3+4). Cancer in 6 out of 17 cores. On right side of prostate. PSA is 3.9. I see on my biopsy report it says Perineural Invasion Present . Which I gather means cancer is on the nerves inside the prostate which in turn means a higher chance of cancer spreading outside. Although not always. I am waiting to be called to St James for initial chat pre treatment choice ( surgery seems best for me). I was private up to this point as I don't have health insurance. My question is has anyone any experience with Perineural Invasion?? And what were the outcomes? Honest answers appreciated. Thanks, Sean

Hi All, I have opted for delayed breast reconstruction because I wasn’t sure if I would require radiation post surgery as well as chemo. I was a candidate for oncotype dx and was hoping I won’t require chemo. However, results came back I would benefit chemo. I am currently on ACT chemo regimen, would complete on Jan next year. It would be of great help if anyone would give me tips about delayed breast reconstruction. My Breast consultant advise DIEP breast reconstruction vs implant. I need helpful tips to prepare me for this procedure , especially from those who have been through this. Thanks a lot! Kind regards, Joi

I'm struggling with the knowledge that everyone in my town will be aware of my situation..I know having breast cancer and being at the start of my journey should make me not care, but I deeply dread people other than my immediate family knowing. Everyone knows Everyone here and what they don't know they make up, my own brother in law would tell everyone and embellish the facts for shock factor and while I have wonderful friends I don't want any help right now as Im still trying to process everything. I'm quite private and feel more in control if no one knows ,so I can still go shopping or my kids school without looks and constant attention. Ireland is a small country so I'm aware that when I start radiation I'll probably meet people I know, but how do I still keep control and keep people at a distance without offending anyone. Sorry for the huge essay