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Hi, I'm nervous posting here. For the past two months my life has been turned on it's head. My gynae referred me for a hysteroscopy due to a thick endometrium. It turns out I have a polyp which will be biopsied and removed. Ok I thought, that's that sorted. Then I received some information about my biological mother's family. My great grandmother, 2 great aunts, and 1 aunt all had breast cancer. So I had a breast exam on Monday. One area of my left breast was quite sore when doctor was pressing. She said that it was "lumpy" but was quick to add not a lump, and told me she isn't worried and I shouldn't worry. I know young women who were diagnosed with breast cancer and who lost their lives to it. I'm 41. 3 years ago I had a mammogram because of tingling sort of pain. Outcome was mastalgia. I'm also newly diagnosed with an underactive thyroid and am taking Eltroxin. I'm very scared. I have a history of health anxiety so all of this is my worst nightmare come true 😥 Thank you for reading.

Has anyone explored the Lu 177 PSMA treatment ? I understand only 3 on trials in the Mater Private. Royal Marsdon in Surrey on hospital in the UK offering it. FDA approved in 2022 But originated in Germany about 8-10 years ago, and is now available in 50 - 70 hospitals in Germany. I have stage 4 metastatic prostrate cancer and am half way through my 39 radiotherapy sessions and am interested in exploring what options are available afterwards to contain / beat my cancer. I’d really love to hear from someone who may be interested in exploring this option or any other constructive options for this journey. Gearoid B 08.10.23

This October is Breast Cancer Awareness Month. While breast cancer mainly affects women, approximately 30 men are diagnosed with breast cancer every year in Ireland. Men have a small amount of breast tissue behind the nipples where cancer can develop. The exact cause of breast cancer in men is unknown but there are some factors that may increase your risk. Breast cancer risk increases with age and most commonly affects men over 60 years of age, however it is important to get checked out at any age if you are concerned about symptoms. Other risk factors include obesity, high oestrogen levels due to other medical conditions, previous radiation to the chest, and a family history or genetic link. As the incidence of breast cancer in men is rare, most men with these risk factors will never develop it. The most common symptom of breast cancer in men is a painless lump in the breast under the nipple. Other symptoms of breast cancer in men and women can include an inverted nipple (nipple turning in), nipple discharge (often blood stained), changes in size or shape of the breast, rash around the nipple area, skin ulceration on the breast, or swelling under the arm. If you notice any of the symptoms mentioned or are concerned about any changes to your chest area, you should see your GP to get checked out. Most changes are not breast cancer but the earlier breast cancer is diagnosed and treated the better. Our website has information on male breast cancer here including information on diagnosis, treatment and supports available. If you would like to speak to a cancer nurse regarding any of this or to get advice or support you can call our Support Line on 1800 200 700, Mon to Fri, 9am to 5pm.

Hi all, Has anyone been for a private triple assessment and then went back to the public clinic afterwards? South east area but would fly to the moon… Also how much would it cost in total including seeing consultant for results etc I am 59 days waiting publicly on an urgent mammogram and ultrasound. I have been told there’s no available dates on the system yet and I will be informed when there is. I don’t feel I will be able to relax unless I have a biopsy. after going through this journey with my own mother who was told scans were good and nothing concerning but had a biopsy same day to be sure. It’s a stressful time.

Anyone know of a group for colorectal cancer survivors? I've a permanent colostomy and have great stoma support, but have never talked to or compared not with a colorectal Cancer survivor!

Gynaecological cancers are those that affect the female reproductive system and include womb, ovarian, cervical, vulval and vaginal cancers. This September the aim is to provide a better understanding of these cancers and their treatments. If you have been diagnosed with any of these cancer types our Supportline has experienced cancer nurses that can answer your queries in confidence. Treatments for gynaecological cancers include surgery, chemotherapy, radiotherapy, hormonal therapy, targeted therapy and immunotherapy. The treatment you will be offered depends on a number of factors and will be explained to you by your doctor and nurse. It is important to understand why you are being offered this treatment and the possible risks or side effects it may cause. Ask questions if you need anything explained. This information may feel overwhelming so remember support is available for you during this time. Your hospital nurse can help you navigate your treatment options and provide advice on managing possible side effects. One possible effect from gynaecological cancer treatment can be the impact on your sexual relationships. Treatment can affect your sexual wellbeing by causing physical and emotional changes. Our website has some information on specific sexual side effects here. Many women feel embarrassed or uncomfortable discussing this with their medical team but it is important to get the information you need. Your doctor or nurse may not go into detail on these side effects unless they know you would like to discuss it so tell them if you have any queries or concerns. If you would like to speak to a cancer nurse for further information, advice or support you can call our Supportline on 1800 200 700, Monday to Friday, 9am to 5pm. There is also a gynaecological cancer resource called This is GO which is an Irish based personalised online resource for women impacted by Gynaecological Oncology(GO).

I am supposed to go for Chemotherapy. The drug being used is Folfox. I was amazed at the side effects while the treatment is being given. It has raised a question as to whether I want to go ahead with the treatment. Has anyone used Folfox and how did you feel during the treatment. Thanks Richard Galway

Hi I am 64 and was diagnosed in Feb Invasive Ductal, Grade 1, Tubular. ER & PR+. Had lumpectomy, radiotherapy and started Anastroloze in March. I am finding the side effects difficult, mainly Fatigue, sleep issues, cognitive impairment and low mood . I also have bone pain, nausea and my bad cholesterol has doubled. I need to work as self employed and live alone. Some days fatigue really bad. I am considering stopping taking this but that causes me more anxiety. I am not prepared to take more medication for side effects or change medication as they all seem to be the same . I am due in Oncology soon and wonder 1 what questions to ask re Risks in stopping/taking and 2 if anyone else has stopped ??. I am trying to weigh up quality of life Vs recurrence risk

We here at the Irish Cancer Society would encourage everyone to talk to their Doctor, Dentist or Pharmacist about any unexplained concern they may have noticed in their mouth or surrounding area. A symptom may be a sore, ulcer or lump in their mouth. It could be a sore throat or a neck lump. Another symptom to be aware of is red or white patches in your mouth, or if you have an unexplained pain in your mouth. If any of these symptoms are there for longer than 3 weeks, we would advise you to get them checked out. Of course, many of these symptoms can be explained and cancer of the mouth is not common. However, we want to make everyone aware of symptoms and to encourage anyone who has noticed a ‘change’ in their mouth to get it checked out. Picking up a cancer in the mouth or the surrounding area early will make a significant difference to the success of the treatment and the person’s quality of life after treatment. Those who have a medical card or have paid enough PRSI contributions are entitled to a free dental examination each year. Unfortunately, if you have neither there will be a charge to see your dentist. If you would like to speak to a cancer nurse about any changes you have noticed or any other concerns, you may have you can phone us on 1800 200 700. We are here Mon-Fri 9-5pm and would very much like to support you through your worries. I do hope we will hear from you. Kind regards Cancer Nurse    

Hi! I hope you might be able to help :) BACKGROUND My Dad is 67, and has been receiving treatment for Small Cell Lung Cancer for 4.5 years. Most recent was radium for a small spot in his head. Besides that his scans have been coming back clear. He has been deteriorating over the last year (severe muscle loss) and the decline has accelerated in the last 2 months where he has lost complete use of one leg, and second leg is not far behind. We hoped that the spot in his head was the cause but there has only been a decline since treatment. Our Oncologist suspects an auto-immune issue but we don't know for sure. He has spent 7 weeks in hospital and now is being moved to pallative care in the hopes he can rebuild muscle there. QUESTION I have heard about LEMS and I was hoping that this could be explored as a potential cause of my Dad's muscle loss. What would be the best way to broach this with the hospital team? Might you be aware of any teams or patients in Ireland that have had experience with LEMS? Many thanks, Andrea