Inoperable
Hi all, I am newley diagnosed with stage 2 invasive HER2 negative ERPR positive and inoperable at the moment(that word really freaked me out) I am currently on hormone suppressant tablets to try and reduce the tumours and see the Oncologist next week. I feel very anxious all the time as I thought when I first heard I had it, a masectomy would be first up but it feels like my treatment is all in reverse and I don’t feel positive about it at all. Has anyone had experience with this before.
Very difficult to listen the Podcast
Hi all, so I started listening to Charlotte's podcast. I just started the Episode 2. While this podcast is fantastic, I find it extremely hard to listen and my emotions just overcome me. I would love to know how is everyone going and what do you do to stay calm and not be a slobbering and emotional mess like me. 😔 Thank you everyone 💓
So it turns out waiting is not for me….
Hi everyone- my name is Jenni and I was diagnosed last Tuesday 28/07/26 with invasive ductal carcinoma and DCIS. I was told a surgeon would be in touch within the week after getting a referral the same day. I have since requested my GPs reception to forward the referral twice - and was met with such hostility I will change doctors. We found out today that the referral was still not sent and hadn't got to where it needed to go. So my husband did a round trip (over an hour as we live in rural Vic) and went and got a hard copy from my GP and took it to the cancer care clinic as instructed via phone- to be told they did not need it yet and he nicely insisted she take a copy and give it to my BC nurse - I am so overwhelmed- how quickly should surgery be happening? I’m sorry to vent but its been a lot ❤️🌸
Fear of the unknown
I have recently been diagnosed last week l had a lumpectomy and nodes removed for further examination and, now l am anxious fearful about the follow up appointment this week. I really would like to become an ostrich put my head in the sand as l am not looking forward to their findings.a difficult day
Today was my PET scan & also a CT scan. Awful. but I did it. I’m just still struggling with the enormity of it all. It’s surreal. I feel like I’m in a bad dream. And on the scan table I was wondering how the hell I got here. I’m scared. I cry lots. I know I’ve posted this before 🫶🏻 it’s good to be able to get it out! Thanks for listening 🌸floundering
Hey everyone Im new here and just found out I have invasive lobular carcinoma grade 2. I’m in shock after a whirlwind 2 weeks of tests. Today it’s hit me hard. I’m 68. I’m now taking Letrzole and surgery is 12th August. I’m having a lumpectomy and although no lymph nodes are involved, the surgeon is taking 3 nodes for testing. I am also dealing with CPTSD and all of this has triggered me. I just cry a lot. I don’t know who to turn to for support. I do have husband & family. I’m not sleeping which doesn’t help. It’s just so overwhelming
Feeling angry
I have recently been diagnosed and had a lumpectomy last Thursday. I’m feel fine not overly sore but tired. Mine was picked up on a mammograms so early and I’m very grateful and know how lucky I am. I’m ok with diagnosis 1 in 7 my turn. The issue is I’ve been through so much recently and I’m finding myself angry. Well the last 2 days. 2 knee replacements, fibromyalgia, depression, late adhd diagnosis at 62, mum with dementia I’ve had to put into care, I sold her house without her knowing which is heart breaking - no help from siblings and that just this year. Lol. I had a breakdown a few years ago through work, got divorced, my dog died and I burnt my nachos the other day. A bit of light relief. There is more but that will do. I’m exhausted keeping a lid on everything. I’ve spoken to my psychologist who suggested Emdr. I’m by myself and just so angry. My kids have their own lives and basically my safe place is my home (with a massive mortgage) and my dogs. I had started a wonderful new business but have had to put that on hold until I find out what happens next. Which is next Monday. This is not a why me post it’s a is it normal to be angry. Not all the time but it’s scathing and my dogs have heard some words that I have never mentioned before. I’m not really good at asking for help. And was disappointed with the support I received with my knee replacements so reluctant to go through that rejection again. I think maybe it’s the lack of control, not knowing where we go from here. Again I know how lucky I am and whatever treatment (looks like radiation and hormone therapy and possibly another op and chemo if it’s travelled) I will gladly do and be thankful. I guess I’m just bewildered and have no idea what’s normal and whats not. And if I’ve honest I’m teary too. Ok I feel lonely and unsupported as well.
Tamoxifen..
Hi I had been on Tamoxifen for 3 months. I'm post menopausal. I'm 64. I started getting a discharge after couple months and heavy feeling in bottom of stomach like having a period again. Haven't had one in 18 yrs. Also diagnosed with ongoing constipation. Told med onc she said get gp to do an xray of pelvis and u sound. Had Gray then trans vaginally u sound. Results..thickened uterus and possibly hyperplasia along with increased uterine volume. I am off Tamoxifen and have appt with Gyno at qe2 in Brisbane on 12th may. I am more nervous of this app than when diagnosed with ILC. Has anyone had this while being on Tamoxifen. I d like to have a historectomy I don't need my uterus annymore then I could go back on Tamoxifen. Stay safe.. Tanya xx
