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Hi all! One friend of mine has recommended to us ( my uncle has prostate cancer ) to try deuterium depletion as a complementary therapy. In some European countries ( he is Hungarian ), well known and used this new treatment, for a while. Searching the internet i have found an article from the Journal of Cancer Therapy related to this topic. "Deuterium-depleted water (DDW) is a new promising agent in cancer therapy. The efficiency of the method is based on the discovery, that cancer cells are extremely sensitive to depletion of deuterium (D) and might cause necrosis of the tumor. The purpose of this study was to show the efficacy of D-depletion in prostate cancer (PC) patients. In the dou-ble blind, four-month-long, randomized Phase II clinical trial the daily water intake was replaced with DDW......Application of DDW is a new opportunity in cancer therapy. Growing evidence suggests that D-depletion might play a role both in treatment and prevention of cancer. In vitro and in vivo experiments confirmed the inhibition of proliferation of cancer cells [25] and the possible cancer preventive effect [26]. Numerous other experiments, including the study had been conducted on mice xenotransplanted with PC-3 cells, proved the anti-cancer effect of D-depletion induced by the application of DDW..." For me it is sound very interesting and promising. We want to try any complementary therapies to fight against cancer. Has anybody heard of it?

Hi everyone, Just a question about my mam! She was diagnosed out of the blue ☹️ with stage IV breast cancer, that had spread to her bones, last June. She’s 73 and very active. She’s just finished 6 months treatment and was told initially that once that was finished, she’d have a scan and they’d work from there. The treatment finished yesterday, she was sent home and that was it. No consultation or communication of what was to come next. I rang the hospital today to get through to the oncologist. They eventually rang Mam and said they’d do a scan next week. And that was more or less it. It’s great to know she’s going to have the scan but I’m just anxious about what that could reveal and if it’s spread more, what does that mean? I was also annoyed that it took a phone call to find this out and be offered a scan date. I completely understand that she’s not the only one and they are so busy but it’s tough not to have any one to one communication when she’s there having treatment. I’d love to chat to someone who knows the ins and outs. Sorry it’s my first post and I haven’t even read through any other threads. I’m at a loose end for her as she means the world to me and especially my daughter, who she has looked after every day since she was born.

I had a partial mastectomy on 18th March. Thankfully I do not need chemo and will shortly have a two week course of radiotherapy. Has anyone got any recommendations on how to take care of the skin on my breast during and after the treatment?

Hi All, My mam was diagnosed with osephagus cancer about two years ago. She had an operation and two set of chemo. However before Christmas she went for a scan and the cancer had spread and she was told to do another set of chemo..but after having one session it has made her weak. Palitive care team are involved..Ive seen my mam recently and got permission from the Gardai to visit her..it's been difficult because we have to wear PPE gear and I would just love for my mam to see my face with out all the gear on..I know we have to bit since she may only have little time left with us..the whole covid thing has destroyed are family communication. Because we are worried our poor mam might get it and she would be sent to hospital where we may not see her because of the virus. I'm in bits I thought the treatment might work and she would get more time with her grand children..I'm grieving already and I'm so scared for her. Any advice would be wonderful. Many thanks xx

Hi, my mother has recently been diagnosed with 3 brain tumours. She is due to start treatment shortly. Both parents are reeling from the news which is understandable. I'm looking for advice on how to have a family conversation about what's ahead, what kind of support we can give each other etc. Any guidance would be very welcome. Thanks.

Hi. My mom was told last week that her cancer has spread to her bowel. Last November it had began to spread to her liver but she was put back on chemo which didn't work. Mom originally had it in the appendix which was removed but chemo was never given afterwards as a precaution. Sadly the cancer came back nearly two years ago. It was gone into the lining of her stomach. She was out straight on aggressive chemo which worked. It was contained and she had a break from chemo for months, we were so thrilled. Then last Aug she was very sick. Couldn't eat and what she did eat she brought back up. She was eventually hospitalised and we were told then that he had started to spread into her liver! Last week her oncologist told her it was now gone into the bowel as well and that she had months. We are all so broken. Her oncologist wants to see her back in April and he said if she is in good form and stronger he might give her aggressive chemo! It's like the last chance. But the last few days it's like she has thrown in the towel. She hasn't been going to the toilet but she hasn't been drinking water or eating either. I'm just so lost and broken, I don't know what to do

Hi, I was at the triple assessment unit in Beaumont on the 3rd Jan, had two mammograms done, and then an ultrasound. I have very dense breast tissue. The Radiologist said there was something not quite right looking on what was thought to be a cyst and wanted to do a FNA. No fluid came out so she did a core biopsy. I have been waiting for the phone to ring but got a letter dated 10th Jan yesterday to come to back to the clinic on 31st Jan. Is this a good sign that its taking so long to get the results? Is 4 weeks a very long time to have to wait for results is this normal? Thanks

Hi, On Feb 21st I met a consultant (privately) who expressed concern upon examining a suspicious mole on the bridge of my left foot. He told me he would get an appointment for me to have it removed in the following fortnight. The next week on the 28th I received a phone call with an appointment made for the Monday March 2nd. He removed the entire mole along with extra tissue surrounding the mole and underneath the mole and informed me he was marking 'urgent' on the tests and he hoped to have results within 2 weeks. Before I left the hospital the nurse handed me information for my GP (I had 2 layers of stitches and the top layer needed to be removed after 2 weeks) and she said it would be 6 weeks before I get the results. It is now nearly 8 weeks and I haven't heard a dickie bird. I understand the Covid-19 is delaying labs and test results, but I thought I would have heard something by now, Is anyone else waiting as long as me?

Hi lovely people, two weeks ago I got that news, it's lung cancer( non smoker),41 yes of age, first meeting the oncology team said PET scan showed it was also in my thyroid, spine and hip bone...I'm starting Chemo this Friday, the reality will kick in then... My question is what questions to ask the doctors and nurses again, suppose a lot of it past me by.... Regards Jessi

Hi, My father has just been diagnosed with Peripheral T-Cell Lymphoma. Just want to speak with anyone with similar diagnosis. He is 69 years old and it seems to be in one node at the moment. Starting chemo next week. Just trying to reach out and see if anyone is in the same boat. Also wondering about the use of CBD oil in conjunction with CHOP chemotherapy, if anyone uses CBD oil or how have they found it? Thank you.