Breast Cancer Now Forum

Hi, I just wanted to share that I was diagnosed with primary breast cancer, grade three, mildly oestrogen positive in March 2010, and although there have been ups and downs since, I'm still (touches wood!) fortunate enough to have no evidence of disease, 7 years on. My boys were 2 & 4 years old then, now they're 9 and 11. I've seen the youngest start primary school and the oldest start high school. This time seven years ago, though, I was a terrified sobbing wreck and totally sure I'd not be around to see this. I had a lumpectomy, chemo, radiotherapy and tamoxifen. I remember so clearly how tough those early days were and the hope it gave me to hear back from members who were a few years down the line and still (more touching wood) doing ok, so I hope that reading this helps someone in the same way! Sending lots of love to you all. Take care xxxx ... View more

Hi everyone, three years ago I posted about reaching my three year anniversary since diagnosis. This week, I reached six years since diagnosis. I had just turned 36 in March 2010. Now I've just turned 42. My Reception class child and my nursery age child are now years 4&6, and I'm so grateful to have been there with Them as they've had their ups and downs, and they've grown so beautifully into lovely lads. I worried so much that I wouldn't be here, and I was so filled with emotion when I looked around secondary schools with my eldest and then when he got in the school we'd put as first choice. I'd given my husband clear instructions on secondary schools as I went through treatment because I was so upset at the thought I might not be here to help my boys at this stage of their lives. Well, I am still here, still ok, lots of ups and downs along the way, still touching Woodard I write this, but I happy. Here's my post from Three Years Ago Today..... I suppose that at six years now, you should just double the sentiments in that post !!!! ... View more

Hi everyone, I'm just bumping this up so that it is easy for people to find. If you are 45 or under , with a breast cancer diagnosis under your belt, and would like to cyber meet other younger women from the UK and Ireland in the same position, you just need to follow this link to our public page. Once there, find the 'send message/message us' button (it can look different depending what device you are using), and tell us a bit about yourself and we can get you added to our network of private, member only chat groups where your posts can only be seen by other members. We have a main group, a moving on group, a living with secondary bc group, pregnancy, fertility, research groups, and regional groups for finding local friends. We've had around 1300 women join us since we launched in oct 2012, so you won't feel alone! The link to our public page is : https://m.facebook.com/YoungerBreastCancerNetwork?ref=bookmarks Thank you to Breast Cancer Care for continuing to support us ❤ X ... View more

I've copied this from the hope inspiration thread where I've just posted it as I thought younger women might like to easily access it. tors Member 3:55 PM I thought I'd pop back to the forum to let people know that I was diagnosed five years ago yesterday. I know these kind of posts used to give me so much hope when I was diagnosed and going through treatment. I used to post on here constantly. There have been ups and downs since diagnosis. I've actually found it really tricky to comprehend the five year thing and, instead of feeling overwhelming joy, it's made me reflect a lot. But generally, other than tricky milestones, im a happy soul! My boys are 9 and 7 now, they were two and four back then. I've been NED since surgery and am so very relieved at that, although to celebrate would make me feel like I was about to activate the "to tempt fate, press here" button! I've copied my first ever post to the forum below. It's been a hard journey but I've made some wonderful friends and had a lot of good experiences that having breast cancer brought to my door. I returned to work, I got back to being an 'on the ball' mummy, I've been on holidays, I've set up a support network for younger women, I've stayed in touch with BCC and help them all I can, as payback for being helped through the hardest time of my life by them. I was a model at the fashion show last year! So I think what I'm saying is that time moves on, things change and there is hope that those with a primary diagnosis will be ok, and there is hope that those with secondary diagnosis will be able to live productive lives for many years as I've met many ladies who do. Here is my first ever post, and thanks for reading x March 2010 Hello, 36 and just diagnosed I was diagnosed with invasive ductal breast cancer earlier this month. It feels like I am living through hell and have had the sh** kicked out of me. I have cried a lot. I feel like my friends are the luckiest people on earth as they are still living the carefree life I was living up til 4 weeks ago when I found my lump. Thats the new me, jealous of my own best friends. I found a lump in my left breast when I was examining myself on a Saturday night, and was given an appointment at the local breast clinic the following monday. I cannot fault my GP and the breast clinic staff so far.Supportive and lots of information. That day I had a mammogram, an ultra sound, a fine needle biopsy and then got the results the same day and was told "it is cancer". My husband was with me . I had to lie down on the bed as i nearly fainted. I had to go home and tell my mum and sister. They were minding my two little boys who are just 2 and 4. Seeing my mum and sister's faces crumple when they saw my face was awful. thank God for my husband being with me. Suddenly I totally depended on him, having whinged about him for years like we all do. I think I quite like him again now! That night I was beyond shock. The absolute worst bit was when I went to bed. Previously I had always looked forward to bedtime, especially as sleep is at a premium with young children. But the second the light went off I started panicking and breathing too fast and had to have all the windows open. My lips and fingers went tingly and it took my husband ages to calm me down. there wasn't much sleep to be had that night. The next morning I was back at hospital and sobbed silently through the ultra sound guided core needle biopsy, although I was still aware enough not to move whilst sobbing in case she slipped and hurt me! The sound of the needle thing clicking was awful and I certainly couldnt watch ( though my husband did), and I hummed throughout to keep calm, so must have seemed mad. But it really didn't hurt as the local was great.My breast was black and blue after though. The thing that really got me was that the last ultra sounds I had had were to see my little babies when I was pregnant and now it was because apparently I have breast cancer. And after a year of my persuading and convincing, my husband and I had finally been trying for a new baby and I had been expecting to have ultra sounds at this time for pregnancy again, not for this bag of rubbish. Thank god that I didn't get pregnant though, it is hard enough wiht just my body to take into account. I saw my breast cancer nurse again after the core needle biopsy and totally collapsed. I was convinced that this was cancer from somewhere else which had spread to my breast, so my body was already riddled. She reassured me this was extremely unlikely but who believes statistics now as we all know that someone has to fall foul of them, and as has already been proved, I am already on the sh** unlucky list.... Waiting for my biopsy results was horrific. The wait in the clinic waiting room was genuine torture. The tumour ( which is a word I really really really cannot believe applies to me) seems 15 by 11mm, and the results indicate its a grade 2, but only "vaguely" oestrogen positive ( 4 out of 8 if that means anything?).There "is no reason to believe that it has spread to the lymph nodes" but who knows? And when did lymph nodes become so important in my life? I don#t think I had ever even said the term a month ago. So now I am waiting. I have my lumpectomy on Monday. When i first heard that I had the dreaded cancer, I told them to take the top half of my body off. At the next appointment I downscaled to a double mastectomy, then a mastectomy and finally have agreed that a lumpectomy is the way to go. I have to have a wire put in via ultrasound to mark the place before the op, and am having sentinel node biposy so need to go to the nuclear medicine department at a different hospital first. Nuclear medicine! Wow, am going to be glowing from that, with a blue breast, blue wee, blue poo and blue contact lenses from the dye! I will be like an avatar, if only they could stretch me to make me taller and skinnier too! although I did lose half a stone in a week through total inability to eat at first. So onward and upward. I am terrified about getting worse news after the op, as i am slightly more able to cope with the status quo now than I was before. I feel that this is totally unfair, I am a good girl , never smoked, never ever taken drugs, hardly drink , not overweight, breast fed both babies for 7 or 8 months until they got top and bottom teeth they could bite with. Have just realised how much I have written, hope I haven't sent anyone to sleep and well done for reading this long if you have! Think I feel a bit better for telling people what has happened to me, although feel as though am preaching to to the converted, coals to Newcastle and all that! ... View more

I thought I'd pop back to the forum to let people know that I was diagnosed five years ago yesterday. I know these kind of posts used to give me so much hope when I was diagnosed and going through treatment. I used to post on here constantly. There have been ups and downs since diagnosis. I've actually found it really tricky to comprehend the five year thing and, instead of feeling overwhelming joy, it's made me reflect a lot. But generally, other than tricky milestones, im a happy soul! My boys are 9 and 7 now, they were two and four back then. I've been NED since surgery and am so very relieved at that, although to celebrate would make me feel like I was about to activate the "to tempt fate, press here" button! I've copied my first ever post to the forum below. It's been a hard journey but I've made some wonderful friends and had a lot of good experiences that having breast cancer brought to my door. I returned to work, I got back to being an 'on the ball' mummy, I've been on holidays, I've set up a support network for younger women, I've stayed in touch with BCC and help them all I can, as payback for being helped through the hardest time of my life by them. I was a model at the fashion show last year! So I think what I'm saying is that time moves on, things change and there is hope that those with a primary diagnosis will be ok, and there is hope that those with secondary diagnosis will be able to live productive lives for many years as I've met many ladies who do. Here is my first ever post, and thanks for reading x March 2010 Hello, 36 and just diagnosed I was diagnosed with invasive ductal breast cancer earlier this month. It feels like I am living through hell and have had the sh** kicked out of me. I have cried a lot. I feel like my friends are the luckiest people on earth as they are still living the carefree life I was living up til 4 weeks ago when I found my lump. Thats the new me, jealous of my own best friends. I found a lump in my left breast when I was examining myself on a Saturday night, and was given an appointment at the local breast clinic the following monday. I cannot fault my GP and the breast clinic staff so far.Supportive and lots of information. That day I had a mammogram, an ultra sound, a fine needle biopsy and then got the results the same day and was told "it is cancer". My husband was with me . I had to lie down on the bed as i nearly fainted. I had to go home and tell my mum and sister. They were minding my two little boys who are just 2 and 4. Seeing my mum and sister's faces crumple when they saw my face was awful. thank God for my husband being with me. Suddenly I totally depended on him, having whinged about him for years like we all do. I think I quite like him again now! That night I was beyond shock. The absolute worst bit was when I went to bed. Previously I had always looked forward to bedtime, especially as sleep is at a premium with young children. But the second the light went off I started panicking and breathing too fast and had to have all the windows open. My lips and fingers went tingly and it took my husband ages to calm me down. there wasn't much sleep to be had that night. The next morning I was back at hospital and sobbed silently through the ultra sound guided core needle biopsy, although I was still aware enough not to move whilst sobbing in case she slipped and hurt me! The sound of the needle thing clicking was awful and I certainly couldnt watch ( though my husband did), and I hummed throughout to keep calm, so must have seemed mad. But it really didn't hurt as the local was great.My breast was black and blue after though. The thing that really got me was that the last ultra sounds I had had were to see my little babies when I was pregnant and now it was because apparently I have breast cancer. And after a year of my persuading and convincing, my husband and I had finally been trying for a new baby and I had been expecting to have ultra sounds at this time for pregnancy again, not for this bag of rubbish. Thank god that I didn't get pregnant though, it is hard enough wiht just my body to take into account. I saw my breast cancer nurse again after the core needle biopsy and totally collapsed. I was convinced that this was cancer from somewhere else which had spread to my breast, so my body was already riddled. She reassured me this was extremely unlikely but who believes statistics now as we all know that someone has to fall foul of them, and as has already been proved, I am already on the sh** unlucky list.... Waiting for my biopsy results was horrific. The wait in the clinic waiting room was genuine torture. The tumour ( which is a word I really really really cannot believe applies to me) seems 15 by 11mm, and the results indicate its a grade 2, but only "vaguely" oestrogen positive ( 4 out of 8 if that means anything?).There "is no reason to believe that it has spread to the lymph nodes" but who knows? And when did lymph nodes become so important in my life? I don#t think I had ever even said the term a month ago. So now I am waiting. I have my lumpectomy on Monday. When i first heard that I had the dreaded cancer, I told them to take the top half of my body off. At the next appointment I downscaled to a double mastectomy, then a mastectomy and finally have agreed that a lumpectomy is the way to go. I have to have a wire put in via ultrasound to mark the place before the op, and am having sentinel node biposy so need to go to the nuclear medicine department at a different hospital first. Nuclear medicine! Wow, am going to be glowing from that, with a blue breast, blue wee, blue poo and blue contact lenses from the dye! I will be like an avatar, if only they could stretch me to make me taller and skinnier too! although I did lose half a stone in a week through total inability to eat at first. So onward and upward. I am terrified about getting worse news after the op, as i am slightly more able to cope with the status quo now than I was before. I feel that this is totally unfair, I am a good girl , never smoked, never ever taken drugs, hardly drink , not overweight, breast fed both babies for 7 or 8 months until they got top and bottom teeth they could bite with. Have just realised how much I have written, hope I haven't sent anyone to sleep and well done for reading this long if you have! Think I feel a bit better for telling people what has happened to me, although feel as though am preaching to to the converted, coals to Newcastle and all that! ... View more