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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

Hello everyone. Hoping you guys could share a bit of knowledge. I had some worrying symptoms in my left breast (dent in breast and nipple inverting). My GP referred me to hospital and I had a triple check appointment last week. They did a breast check, mammogram and ultrasound. They told me at the end that my results were fine (other than a few cysts) and no follow up would be required. However im after getting another appointment card in the post for October. This one is an afternoon appointment which is when they do their review appointments. Googling brings up nothing about review appointments, all the phone numbers the hospital give go straight to voicemail, and I havent had an answer to the email I sent. Can anyone tell me what a review appointment is for? Im worried they've now found something concerning on my scans or now think the black spots on my ultrasound arent cysts after all. Thanks in advance.

Would be interested in hearing from anyone that has had their breast implant removed because of Capsular Contractor and have not had the implant replaced. Also, anyone that has been diagnosed with Breast Implant illness?

Hi St Vincent's in Dublin called me to say my appointment is scheduled for next week. ( my gp sent in a referral) I was suprised to hear from them so soon so I didnt properly take in all the info the really nice lady gave me. She said i will be there for three to four hours and if i need a biopsy they will tell me the following week? Is that how it normally works and does everyone usually have a biopsy regardless of their diagnosis. Thanks so much in advance x

I had my first cycle of Taxol on Wednesday last week. Had 4 cycles of AC previous to that. Tough days were had. I'd read that taxol is a walk in the park after AC. Not for me. Suffered horrendous bone and joint pain along with pelvic pain from 2pm two days after taxol. I had to contact Oncology ward to seek advice Re pain management. Upped oxynorm every 2 to 4 hours, it barely touched the surface of the pain. Sleeping tablets were the only way I could get sleep. Meeting with a Registrar tomorrow to discuss my options, lower dose, weekly dose instead of 2 weekly. I just know I could never face that pain again. Saves to say don't believe everything you read as we are all different. I can't help but think I've had 4Ac, 1 taxol, do I really need to put my body through more of this, as it's an insurance kind of treatment to make sure the cancer is wiped out. I know I'm wiped out. Let's see what tomorrow's discussion brings to the table.