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What do you do if you find out 2yrs after having breast cancer that your surgeon deliberately lied to both you and your gp.. was told by my surgeon that the margins were clear after a 2nd operation within a week and then just this weekend I discover that the margins haven’t been met 0.6mm from the superior aspect of the medial shave Have been told that this has put me at higher risk of recurrence

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?

Greetings I am a Gleason 8 (3+5) PSA 10. Apparently I am T2C N0 M0. The cancer is 1.8cm along the anterior of the prostate. It seems to be contained within the prostate. The radiologist recommended IMRT and this seemd fine. However, i saw a second radiologist and they said, given the grade and extent of tumour, they would suspect that micromets could be beyond the capsule and they recommend radiation not only of the prostate but to also include the lymph nodes. Now in terms of risk management the latter approach seemed sensible but of course risks of damaging the surrounding areas will increase. I am at a loss as to what to do!

My Mam was diagnosed with cancer 18 months ago. My world has been turned upside down. I feel so alone and numb. The treatment she has had so far has failed and the cancer has spread through out her body the Car T cell did not work. I was told today that it’s really aggressive and less then 5% she will make it. My Mam has always been my best friend we live together and do everything together. I don’t know how I would survive if anything happened to her. If anyone is going through a similar journey or can advise where I can get support please reach out to me I am so numb and overwhelmed.

Good Afternoon, i have had a double masectomy, and have two prosthesis i find them very heavy and hot can someone recommend a lighter one please.

Hi all I had a head Ct in dec and thought nothing more of it as it came about from an off the cuff remark about headaches . I assumed these were from ongoing treatment tdm1 and just happened to mention . Anyway when I’m last week for treatment I was given the shock that they had found something on the Ct . It’s very very small and I’ve been told highly treatable if it’s something to worry about . I’ve now to have head mri to find out what it is exactly . To say my anxiety levels are through the roof is a massive understatement !!! Mri may not be for at least 3 weeks yet which is torture . I’m so so upset as am due my last treatment in 2weeks and had dared to get a little excited . Every time this time round that I have gotten to the finish line I’ve been tripped up . Has anyone had anything similar which turned out to be nothing ?? This is my second breast cancer diagnoses (I was a month off 10yrs clear ,it came back in recon breast in same spot ). Please any advice greatly appreciated . TIA

Hi, i have been diagnosed with breast cancer. I was wondering if ketogenic diet is good for me or should i stay with balance diet.

I have been diagnoised with prostate cancer I had a biopsy and have been referred for a TAP CT & BONE SCAN. The request went in from the consultant 10 days ago and i have been told it could take8/10 weeks to get the scan done in St Vincents Hospital. I wonder is there anyway or anyhow i could get the scans earlier

Hi everyone, I was just wondering if anyone else had a similar experience. I finished two weeks of radiotherapy the end of July this year. I had mild side effects, like itchy skin, redness, breast feeling hot. They disappeared about five weeks after. But for the last six weeks or so, it has come back stronger than before. I am still moisturizing twice daily and doing my exercises. But my breast has become slightly bigger than the other one, is painful, itchy red and sometimes feels warm. I was referred back to the breast clinic but was told it's from the radiotherapy and to take paracetamol. I honestly felt fobbed off by the doctor (not my breast surgeon). Has anyone advice on what product to use? I am using Aveeno at the moment. Has anyone experienced something similar? Its really getting to me now, and I don't sleep well, due to the pain. Thanks for any advice

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