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I’ve had a biopsy to remove a mole and was told my GP would let me know the results in 4/5 weeks. I receive a letter from the hospital five days after my biopsy to say that I am due a review appointment in a month. I was meant to have the review appointment in two months. When I rang to find out why my appointment had been changed, I was informed that the consultant had asked for it to be moved up to a sooner date to recieve my biopsy results. Now I am worried it could be bad news, anyone ever go through something similar? Any advice would be amazing. I know I shouldn’t focus on a negative outlook but I’m so worried.

Hi there, I’m hoping someone can help me. I had surgery almost 4 weeks ago to remove a tumor from my abdomen. No biopsy was done in advance as it was growing quickly and consultant didn’t want to delay removal. I was told to expect results within a week. To date nothing... I was updated that they are waiting for the immunohistopathology results before report completed but that was over a week ago. Has anyone experienced similar delays? And, if so, how long? Thanks so much.

Hi. My 83 year mum went for a bone marrow biopsy 4 weeks ago now. She had multiple myeloma over 10 years ago and they now believed it has returned. We were told that the bone marrow biopsy would be back in 2-3 weeks and we have heard nothing from her consultant or team. I feel from day 1, there was very poor communication and care this time round. Its incredibly stressful, especially with the correct situation. Who or how can I get information from her consultant and what's the time line from tests - diagnosis - treatment??

I've been given months Diagnosed October last year Had R-Chop and R-Ice - both failed Now on palliative/maintenance chemotherapy What does all this mean for me ? Regards Cora Lawless and Thank you.

Dealing with a cancer diagnosis in normal times can have a huge impact on you. It’s common and understandable to experience emotions such as shock, sadness, anger, fear, worry and loneliness. Read the first of our Support Line blog posts written by one of our cancer nurses here - https://www.cancer.ie/about-us/news/are-you-feeling-lonely-and-anxious-about-your-cancer-with-covid-19

My mum has just been diagnosed with Lymphoma relapse stage 4, but that's all we know because they can not operate as she is very frail, she had Non-Hogkin's Lymphoma back in 2009, and she had beaten it, only to return in her chest (though again, not 100% sure which it is) they can't do Chemo as she is not going to be able to handle it. we are not even sure that she would be able to handle Radiotherapy, we are waiting to see the Radiotherapydoctor who will check and see if she is able to that but the outcome looks bleak. I'm just numb, have been just getting on with it, and being a good daughter and carer.

I had my last chemo on the 25th of September. Although I didn’t lose all my hair it thinned out a lot. When should I expect it to stop coming out??

My husband was diagnosed with osophageal cancer in Dec 19 had surgery in April and was told in June all looking good go home see you in six months. He continued to have pain and a small growth appeared on his scalp. We were told the pain was muscular and the growth was a cyst... in July having pushed for investigations ourselves he was diagnosed with stage 4 cancer with multiple metastasis in his bones. Th is is extremely rare which is why they dismissed the pain. this does not make it any easier. Anyhow three months on 14 weeks of chemo and he is so thin it is frightening, he has no appetite and his energy is fading fast. He gets steroids for the three days he is on chemo and gets good energy, then he is of them again, no weaning and crashes. He is under care of home care team and they are reluctant to leave him on steroids because of long term affects. He doesn't have time to have long term affects. He also sustained a radiation burn to the area around h is anus and though the skin is healing he still has a lot of pain. Any advice from anyone please. Please do not start telling me about small meals snacks etc I have been there done that. Thank you folks, I am coping most of time but at the moment watching him fade away is doing my head in and I don't feel supported by the home care team just now.

Having my first chemo on Tuesday any idea what to expect or tips about it xx

I am having chemo treatment for breast cancer and have 2 children under 12. Myself and husband have gotten flu vaccine but pharmacy said that children version is live and not to be given to anyone on cancer treatment. My gp has advised I should get it done. So totally confused.