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Hi I never posted in anything before so here goes, I was diagnosed 6 years ago with dcis with mi, sentinel node clear, I had a mastectomy and no other treatment. I've had pain in mastectomy side on and off but since August it got worse. My gp sent me for an ultrasound in breast clinic. The radiologist seen a swollen lymph node and done biopsy. Got the results Tuesday, cancer cells in node. I had a ct and bone scan since, I'll get results Tuesday. Has anyone had anything similar. Im so scared. Thank you

Hello, I went to my GP with a small lump in my right breast and a referral was sent to the Mater Hospital clinic for review. I have been waiting 10 weeks now for an appointment and told there are delays because of Covid19. In the mean time a larger lump has developed in my left breast and I have noticed my breast is larger and feels heavy. I cannot lie on my front due to pain in both breasts. I am wondering if I should revisit my GP or continue to wait for an appointment? Also, during the clinic visit will both breast be reviewed or just the one on the referral? Kind regards.

Hi all, I have recently gone through the whole diagnosis and surgery element of breast cancer. I was fortunate enough to have caught it early after a screening and was told I had a 2mm tumour removed. Thankfully it wasn’t in my lymph nodes. I am still finding my feet about information on post-surgery with radiotherapy and treatment. I have just began Tamox 20mg and am quite scared with how many side effects are listed on the patient information leaflet. I’d really love to hear from others who have or still are going through the treatment and see real stories about the drug. If anyone also has any tips on dealing with treatment day-to-day I’d be so happy. It’s been a scary few months and I am trying to stay positive but it is hard. If anyone could give me an insight, I’m keen to hear your stories 💗 sending best wishes to all of you through these times

Hi all, It is 18 months since I was diagnosed with Breast Cancer (Triple Positive). A mastectomy (Including lymph node clearance) in May 2019, Chemo (AC and Taxol), Radiotherapy and Herceptin all behind me. Each of these was a challenge, however the biggest unexpected challenge for me is Tamoxifen. I have a history of Endometriosis which had calmed down, however when I started Tamoxifen in August it triggered the worst symptoms of Endometriosis I ever had within a matter of days. This was only addressed through stopping the course as agreed with the Oncologist. It hasn't gone away, but it is manageable. I am 48 years old and in peri-menopause. I am at a crossroads and I have no idea where I go from here. When I look up alternatives to Tamoxifen all I can find is solutions for Women who are post menopause. I cannot go through the pain again, there is no point in taking a medication if the side effects are impossible to live with, for me it was worse than the chemo. I am hoping that somebody out there has been on similar journey and has some advice, some information that can help me understand a way forward, before I meet my Oncologist in a weeks time. Many Thanks

Hi I was diagnosed with stage 3 breast in August 2020 and my life has changed ever since I went in for an ekg in early July yearly requirement for my job physical and the doctor said that my results showed I had a heart attack he an I both agreed it was false reading but stated to be on the safe side see a cardiologist which I didn’t because I know I didn’t have one...little did I know this was a warning sign Well in August I went for my yearly visit to the gyno and durning the check doctor noted she felt a lump on my left side the next week I was scheduled for a mammo and us then a few days later went in for biopsy an another mammogram My result came back showed I had breast cancer I request to go to MD Anderson instead of local doctors. My mass grew within two weeks from 2cm to about 6.5cm my ki-67 is 70% my cancer is very aggressive I was very scared worried a would die fortunately I was but in the hands of wonderful doctors My treatment plan is 4 ac every 3 weeks and 12 weekly treatments of taxol. I have severe nausea I am taking zofran and comp. I’m only on 2nd ac but my mass has shrunk drastically after my first treatment I do receive steroids bf infusion I started losing my hair after my second week of chemo, I’ve had night sweats and joint aches I do have a port installed on the right side of my chest since cancer is on the left I will also have to have a mastectomy and radiation Today I was informed from genetics test that My bc was gene mutation not sure if it came from mom or dad and that I might want to consider double mastectomy because I am now high risk and later on down the line I’m at a risk of ovarian cancer...I have 7 yr old daughter an at the age 18 will be screened for cancer every year Out of all this I have a wonderful support team hardest part for me is the nausea, working full time , and trying to stay positive because chemo does cause depression almost everyday I have family or friends texting and calling checking in. My mom is a two time Breast cancer survivor She had it in 2001 and 2011 (Had mastectomy in 2011) took genetics test came back negative technology has changed since 2011

Hi Everyone I had Breast Cancer 10 1/2 years ago; diagnosed at the age of 35. I am coming off Tamoxifen in November this year after 10 years on it. My Cancer was Triple Positive. People are telling me about the benefits of taking Turmeric with Curcumin Supplement as a security for it's cancer preventing properties. But when I looked up should a Breast Cancer patient take this supplement it states that curcumin might act like the hormone estrogen. I am confused now, I had ordered a years supply to start when I come off tamoxifen but don't know what to do now. Anyone any further information on this.

Breast Clinic I was referred to the Breast Clinic Eccles St 3 weeks ago, for a thickened area in my breast. I attended my appointment yesterday and had a mammogram done. I was expecting to see a Doctor and be examined and perhaps have an ultrasound or biopsy which didn’t happen. I thought there must be some mistake here. I was then told I would wait 3 weeks for results of the mammogram, It’s so worrying and stressful and the system seems to work so slowly. If I go private for a triple assessment would I be able to be treated in the public system if there is was a problem.

Hello All, I recently found a lump on my left breast and had it looked at by my GP. She said it didn't seem craggy but sent me anyhow for a mammogram and ultrasound. I went in a tad worried but filled confidence at the same time that everything was fine. However, while mammogram showed up nothing the ultrasound was cause for cause for concern and I had a biopsy done there any then. They gave the lump a bi rad 4 rating. From what I've read this has more of a chance of being benign but I'm so so scared. My tumor is 8mm and they said from what they could see it didn't go to the nodes....is this something they need to double check or are they sure from an ultrasound. This waiting a week and a half for results is just awful. I'm crying all the time and just can't work. I have 3 small kids and I want to be strong for them but I'm finding things tough. Blessing and good luck to all. Xx

Hi there, In April 2018, I was diagnosed with Breast Cancer, had Mastectomy- one breast removed 7.5 cm Tumour, then Auxillary clearance, port inserted, 6 months of Chemo and 15 Rounds of Radiation, on Tomoxifen. All good, thank God now. I was 46 at the time and after the first round of Chemo, I was put straight into Menapause. I actually was having a period when they did the first AC round. That was it and I was put straight into menopause. I had unbelievable hot flushes, night sweats. I started putting on weight and I cannot loose it. I tried going back to weight watchers but not a stir...it's like my body has shut down and I can't get it going again. It's so frustrating. Has anyone else has this experience and were you able to find a way to get the pounds down. I always was able to do that with weightwatchers ( more so than Slimming World). I have to say that the 2 issues are the hot flushes still....and weight gain. As you know, we can't take anything with Estrogen to help. Is there a way?! Help. Thanks,

Hi all. New to the forum! Diagnosed with breast cancer 2.5 years ago, single mastectomy and my chemo treatment, which I finished 18 months ago. Still on the wait list for a reconstruction. I’ve been thinking a lot about moving forward and I’m reconsidering having the reconstruction at all. Has anyone been in similar situation? Anyone not had a Reconstruction done and regretting it or happy with their decision? Any thoughts would be a help! Thank you x