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Hi, Not sure if anyone watched nTionwide on rte tonight, quite interesting about breast cancr groups. I am so not in the habit of exercising on mt own as I would prefer to go to the gym, I enjoy step and Zumba, but was advised nit to due to risk of infection. Does any one knoe of walking groups on Northside of dublin, I really do need toget off my ass and exercide when I can that is. Thanks hole all are keeping well. Only 5 more chemo to go as from today, over half dome. Woo hoooooo.

Hi, just wondering if anyone getting this regime. It's the 5ffu, iricantin and oxyplatin. I'm h each d ing for cycle 6 on Wednesday. Seems most people are on combination of two but not all three. I'm 43 yr female with stage 4 colon cancer. It's the first time I've posted on any boards but really would like to hear from someone on this "cocktail"

Hello there, I recently had a kidney removed due to a 7cm tumour. The whole kidney, adrenal gland and lymph nodes were also removed. Two further lymph nodes were detected under my collarbone so as a result I have been prescribed Sutent as part of a long term treatment plan. I would love to know of anyone on similar treatment. Thank you 37 yr old mum of 3

Hello everybody! has anyone experience with cancer vaccines of immunotherapies?

I would like to have views on a very pointed question, without value judgement please. I am male and have just had unprotected sex for the first time with a woman who has not been my normal sexual partner. It was protected sex, but the condom broke, unnoticed, but Im guessing about five minutes before we finished. This woman then advised me that she had had cervical cancer some years ago and described a procedure whereby it was burnt off. She also advised that she had done a screening last year which showed that she does not still have the HPV virus. My concern is for my normal girlfriend who expects to have unprotected sex with me. Am I putting her at risk if I have unprotected sex with her. I am circumcised. What I have read seems unclear. I read that the PAP smear does not detect different HPV types. I read that curing cervical cancer does not cure HPV. I read that HPV causes almost all cervical cancers. I read that as a male I cant get tested for HPV. I read that even condoms don't fully protect against HPV. It kinda reads as if once you know you have cervical cancer causing HPV, you shouldn't have sex any more ? Informed thoughts please.

Hi All, I'm a four+ year Prostate Cancer Survivor and I'm running the Dublin City Marathon on Monday next. My main aim in running this, my third Dublin since surgery, is to provide inspiration to those facing Cancer in their lives. I'll be running with a "Cancer Survivor" strip on my singlet and hope to run around 3:20-3:30. There will be lots of other Cancer Survivors out on Monday, along with thousands running to raise funds for Cancer or running in memory of a loved one. Come on out and give us your support on Monday morning! [url:2tluw33l]http://www.mycharity.ie/event/john_quigley_ics_dublin_marathon_2012/[/url:2tluw33l]

Hello, My experiences in the world as a cancer patient are all listed below. It was a tough year but so far I, with the help a surgeon, an oncologist and an army of wonderful nurses I have come out the other side. I feel altered but normal enough. After the chemo ended (Jan of 2012) I was very toxic with a body in complete turmoil. I had an itch all over my torso and this was harder to live with then all the chemo and ops put together. I was also unable to sit still for more then a minute. I remember being very upset when I couldn't get through a little book with my 3 yr old on my lap. I had to walk up and down the room whilst talking to people. I also looked like a chipmunk as a result of putting on weight after the steroids. I then did a detox diet which someone close to me (in the medical Field) designed and as a result, my itch vanished, my excess weight went and I felt non-toxic again. Joy of Joys, I could once again sit and read a book with my child on my lap. That diet and that man are pure brilliant. I truly believe that if you want to cleanse yourself post treatment, a full on detox is so necessary. It is now 6 months later and my diet has slid back to somewhere between super healthy detox and not great. The reason i write is because I am now having a warm tingly feeling all over my body which has intensified in the last fort-night. It is not unpleasant but it is quite intense when I sit still and am not moving. I intend to phone my oncologist tomorrow for advice but I want to know has anyone else experienced such a sensation. Thanks in advance for some advice Breast Cancer, Practically triple Neg Non-ductal invasive 6 x tc Masectomy to left Breast 7cm + tumour 5 x CMF Ovaries and Tubes removed in July 2012

Sadly a friend of mine is having serious dental problems post chemo so I thought I would let any of you having chemo at the moment know that the dental advice we get during chemo is for a very good reason. Apparently when the white blood cell count is low the body cannot react to some infections and we can be totally unaware that there is a problem. Here is what I was told. Please add more tips if you know more! - Brush after every meal with a soft toothbrush - Use gentle mouthwashes to avoid ulcers - Drink often to avoid a dry mouth (less saliva means less natural cleaning action) - Avoid chewing gum for extended periods of time as this encourages continued chewing action during the night which stresses the teeth - Avoid sugary drinks, crisps and any food that sticks to the teeth if you cannot brush your teeth right after a meal for some reason. Take care! Hugs Kathleen

Hi, I am receiving treatment for Metestatic breast cancer in my bones and was wondering if anyone else is going through this at the moment, I would like to compare notes etc as I feel on my own at the present even though my family are great. What questions should I ask my oncologist? I am on Zometa every 4 weeks and have just finished my 8th session

Hi everyone! I'm new here and what a wonderful service this is. I'm not sure where to post this as it doesn't fit with any of the topic headings listed. I'd love to hear if anyone has experienced a delayed shock and grief of their cancer journey? I had a cancer diagnosis and several bouts of surgery in 1999 for cervical cancer and only very recently have felt very low and shocked and sad when I look back and wonder how I got through it without any help or much support..... my family barely mentioned the 'c' word; or even still hardly mention it. My husband never mentions it (we hadn't met back then) and sometimes I feel that he doesn't understand my pain and loss and what I went through, and I don't know how to tell him. I'm always conscious of my health and I really take care of myself, but the fear sits with me always of cancer returning. And in that, I feel that my husband doesn't appreciate me and my now good health and that perhaps our time together is precious. I know I'm going away from the topic but I am so so surprised at my sudden reaction to all this. Thanks for any guidance