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Hi I am hoping someone can help me. My mam went in for routine apt in hospital for her heart (she hasn't had one for 2 years due to covid). They found shadows on her lungs which was not like something that would be found in the lung. It was found to be breast cancer and she has spent last few weeks in hospital and was transferred to the mater and then released. We have now got word that she has apt in Tullamore hospital next week. She is on oxygen now and very weak. The original cancer was breast but now in lungs and lymp nodes. Can you please advis of what questions to ask the doctor at appointment..they have already told her that they will not be operating but that is all we know. Thanks for any advice just a bit lost

Hello I have finished 4 x AC Chemo sessions and am starting weekly Taxol and others Chemo sessions from this week. My daughter is and there are cases of Covid in her school. The school are great and communicating with parents - so I kept herself off for the last 10 days. I also don't want her to miss out too much - and am in a quandry as to send her back in or not. What are others doing? Thanks

  November is International Lung Cancer Awareness Month There are approximately 2,500 cases of lung cancer diagnosed in Ireland each year. Lung cancer is the fifth most common cancer diagnosed in men and women. It is important that we are all aware of the symptoms of lung cancer. The symptoms of lung cancer can include the following: Coughing up blood A cough that doesn’t go away or a change in a long term cough Repeated chest infections that continue after antibiotics Pain in your chest especially when you cough or breathe in Unexplained weight loss or loss of appetite Difficulty breathing A hoarse voice or difficulty swallowing These symptoms can caused by conditions other than cancer. It is important to have any symptoms or a change in a symptom reviewed by your GP. Detecting cancer early can make a difference. If you have any questions or concerns and would like to speak with a cancer nurse please contact our Support Line on 1800 200 700, Monday – Friday, 9am -5pm. Kind regards, Cancer Nurse  

Hi all, I attended the A&E about 3 months ago because of a hard lump and pain in my neck and my voice is hoarse too. The doctor told me they suspect cancer and are concerned for me and they needed to see me within 2 weeks but I later received an appointment letter for 4 months time. My pain got worse and I started losing weight unexplainably and feeling generally unwell. GP later sent me for an ultrasound which showed a solid nodule in my thyroid. He sent the hospital a letter for me to be seen urgently but no word yet. Prior to this, I have suffered from an undiagnosed severe abdominal pain and constipation for 5 years and colon polyps were found over 2 years ago. Please can anyone advise me on what to do because I think I am having a serious health issue that needs an urgent medical attention. Thanks!

Hello, I am have been through mastectomy, chemo and rads. Its been a rough journey with lots of side effect during treatment and a visit to hospital for infection. Anyhow I'm now out the other side - 12 months on, and I started in Tamoxifen 2 weeks ago. Thing is I am getting bad headaches since starting this med- I know it was noted as a possibly side effect. Just wondering if anyone else went through something similar? How long will it take for the headaches to ease? I'm also more tired than usual but tbh the headaches are bothersome. Hot flushes too but nothing too bad. Thanks :)

Hope this is okay to ask here, I'm looking for some guidance re results. Sorry if this is long winded! 15 months ago, I had my gallbladder removed. Prior to surgery, I really cleaned up my diet as I was quite overweight (mainly bc I was so sick if I ate anything fatty) and upped my fitness. I lost near 2 stone in 2 years. When I had it removed I felt amazing, the gallbladder pain was completely gone. I started to eat a bit more freely and stopped loosing weight but also wasn't gaining. Fast forward about 6 months from gallbladder removal, I started to feel sick again. I had loose stools daily, serious urgency for toilet and colicky pain all over my abdomen. I put it down to my body getting used to no longer having a gallbladder. Then I noticed I was loosing weight, I thought great as I had wanted to lose more. The stomach pains and the lose stools just kept getting worse. I could barely leave the house without fear of where a toilet would be. My stools are often very dark (not black but dark) and tarry, with sometimes mucus. I put off going to the dr for many many months as I had a very sick family member who was my priority. My family and partner all had a chat with me as they were concerned about the weight loss, I was down 2 stone in less than 10 months with basically zero exercise and vomiting on and off and still having toilet issues that were getting worse. I made an appt in November with my GP(it was my first time with this GP as she is new to the practice). My GP said that the weight loss, toilet issues and pain were slightly concerning. She sent me a referral for ultrasound, colonoscopy/EGD and bloods. All bloods were normal, incl. coeliac disease. Ultrasound was also normal apart from gas obstructing parts of pancreas. I then had my colonoscopy mid/end December. I was given the report/finding sheet after but not much was said. There was a total of 16 biopsy taken, no polyps found but they did find a mass at cecum, 2-3cm away from appendix. It was said that I need a CT TAP to characterize and that I need to see my consultant(I haven't met him yet as the coloscopy was in a different clinic and my appt was rushed through) with biopsy results and CT results by February. They also took FLT bloods, U/E, FBC, which worried me bc they didn't seem to do that for anyone else. I completely put to back my head for Christmas and didn't give it a thought. I rang my GP yesterday for my results. She asked had the DR discussed and I said that I received the findings but no one talked me through them. She went on to say that only some the biopsy results were back and that they were normal. She then asked me did I know a mass was found and I said yes should I be concerned. She said well yeah it is kind of concerning, which absolutely floored me as I had just been ignoring it so far(coping mechanism) I then said I haven't received a CT appt and she urged me to contact my consultants secretory asap. I rang the secretory today who was very nice and as soon as I explained to her she told me the biopsy results has just come back this morning. And that she will arrange my CT and APPT for as soon as possible. I was happy enough with that but then started thinking about it too long and thought okay if they have the biopsy results then surely that will tell a lot and they should let me know. So my questions are: 1) Would it be appropriate to ring the consultants secretory again and ask where and when I will receive biopsy results? as I'm so anxious I just want to know now or would my GP also have them now, would it be possible to ring them for the results? 2) If biopsy is (hopefully)good news why would I need a CT TAP? is this standard to organize CT TAP regardless? 3) What are the possibilities this mass could be? 4) Has anyone else had a similar experience? I cannot imagine waiting much longer for results bc its driving my crazy since I spoke to my GP Sorry for being so long winded! Anyone reading this with concerns for their health, please please go speak to your GP, do not put it off like it did.

HI. Just wondering if anyone has managed Liver Cancer pain with Canabis Oil? Been reading it might be helpful in certain circumstances. Unfortunately current medications are not providing relief. Thanks for any consideration.

A number of weeks after receiving first two Covid vaccine a mole emerged on top right arm. Kept an eye on its development a number of months later got a private appointment with a dermatologist . Got it taken out and it was determined to be Stage 1a melanoma and two months after that got appointment for wider excision and told got everything. Follow up is with dermatologist every 3/4 months and he is checking lymph nodes - no ultrascans suggested - it fact just this. . Question: I keep hearing about a protocol care pathway for melanoma cancer which is the same for public and private patients but no one can give me documents or information has given me any information . I am reading all sorts of research documents on links with Covid vaccine on the internet and now getting very concerned . has this come up in this forum before

I recently finished chemotherapy prior to surgery for breast cancer. As the response to chemo wasn’t as good as expected I am now being put on a treatment called Kadcyla instead of herceptin. I’m worried about the side effects of this drug. Any insight would be greatly appreciated.

So breast cancer? I’m currently awaiting my triple assessment but have a strong family history so I’m quite concerned . I have a lump above the nipple about 2cm deep enough down and my breast is leaking a creamy to cloudy discharge the past while. Just wondering what symptoms you all had before your diagnosis ? I know everyone’s journey is different but I’m just curious Thank you