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Hi my name is Alice and Ive got breast cancer. Im attending St Vincents hospital for treatment. So its in the left breast and got into lymphs. Next step is CT scan then chemo, then op then radiotherapy, for now fingers and everything crossed. I am 47 years of age.I would like to ask another wou for man who had a similar diagnosis and has already travelled this road for a chat? I am very grateful to you in advance and thank you for reading my post. Alice x

Hi there. I was given a colposcopy in UHG and am now being transferred under gynae to St James's in Dublin. I have a CT booked with Galway, quickest appointment in January. James's have received my referral but does anyone know how long it usually is to get an appointment to see a doctor? I don't want to be asking the secretary so I'm wondering if anyone here might know from prev experience?

I recently had a colposcopy where I had a biopsy done. My doctor told me I'd have to have a LLETZ treatment. My biopsy fro colposcopy said I was stage 1a1 and done the LLETZ. The doc then rang me and said I am 1a2 and I now need to be transferred for scans to another hospital. I'm extremely confused as the doc told me that I would only need a LLETZ or worse case a hysterectomy. I'm concerned as when I was initially diagnosed she was saying all I would need would be another LLETZ and now it's gone to scans. I didn't realize I would need scans at this early 1a2 stage....

Hello all, My husband, 43, has been diagnosed with a stage 4 gastric Cancer last week! We were shocked as he had no symptoms other thank an occasional heartburn. We were told it was probably caught early given his young age, no symptoms and general good health. How I wish that was true! Last week the scans showed it has spread to the abdomen area and we were told it is no longer operable! Here I am writing to you desperate! We have three kids age 12 and under (youngest is 1.5). We are both foreigners living in ireland for 15 years now and have no family here! I am terrified of what is to come 😱😱😭😭😭

Hi, I have recently been diagnosed with prostate cancer. The urologist has informed me it is at the early stages thankfully with a score of 7. He told me I had three treatment options available to choose from. Surgery, External beam radiation or brachytherapy. My initial leaning is towards the brachytherapy following a discussion with the urologist. I will hopefully meet the oncologist in the next couple of weeks to discuss the options further. Has anyone had this form of treatment? The research I have read indicates it has a quicker recovery time with less side effects. Is this the case?

Hi there, I got diagnosed with nasopharyngeal cancer on 28 Oct and have started treatment 3 Dec - for 35 treatments including 1 day each week of chemotherapy. In 2018 I had a virus which led me to have a dull hearing in my left ear and a runny nose. 2 years later I have a 43mm tumour in the nose cavity and has travelled to lymph nodes in neck. Its a rare cancer and I hope I can get shut of it this way. does anyone have anything like this?

Hi I’m just wondering how long you be waiting to meet with your oncologist? I had my surgery (lumpectomy) on 28th July and my follow up appointment on the 12th August and was told I’d be meeting with my oncologist to discuss starting chemotherapy but i haven’t received any appointments yet. I’m just eager to get started.

We run a Facebook (Private) support group for all those affected by Lynch Syndrome. I have inherited one of the predisposition Genes (MSH2) and know how hard it can be to find information and navigate the medical system. We are also aware that the current system is far from perfect and can be confusing. When you are trying to understand your inheritance or potential inheritance and navigate the medical system we believe speaking to others in the same boat who really understand can make all the difference . We are a caring group of people there to listen and offer support . Anyone can find us by following the link below or entering Lynch Syndrome Ireland you will be directed to our open Facebook page. https://www.facebook.com/lynchsyndromeirl/

Hi all. I was diagnosed with CMML 1 on June 2nd, all very new and scary. Anyone else out there with Leukemia? Take care Lea

Hi My name is Claire and I diagnose with breast cancer . I had the operation where they remove the cancer and one lymph node which came back postive. So the sent it of for Oncotype DX which came markers 12 which is very good. But because of new research they co.e up with two options and my makers where low Im 50/50. So i have to decide whether to get all the lymph nodes removed radiation treatment and tablet but they say Im high risk of getting lymphedema. Or not to have the operation and just have radiation ct scan ones year and tablet . So I dont what to do has anyone else come across this Claire