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Re: Who's starting Radiation in November 2025? Let's gather here to share!
Hello@nope123
Thank you for your message!! 😊
First off, it is great that you and your husband were able to have a getaway. So great for the mind, body and soul to be in a different environment and enjoy beauty!
I absolutely LOVE walking the trials we have close by, and being in the forest. But winter is upon us and I live in Ontario, Canada, so that may be a bit difficult walk, although not impossible. As long as it’s not icy ! haha
Thank you for sharing on how you are feeling. Happy to hear that you are feeling better. Like you said, it’s a marathon and we will finally make it to that finish line in terms of treatment. And I was told by my team that the side effects are gradual and build up over the course of treatment and the “worst” is about 2 weeks after the last radiation treatment, which sounds in line with what you described.
I am most worried about the fatigue. I am off work til the new year so me being home and resting is on the books for me.
Good news!!
I heard from the Cancer Centre yesterday. I am restarting on Thur Dec 4th. Isn’t is crazy that I’m “excited” and a bit anxious to restart and then just want to be done with it!!
Just the whole process.. checking in, getting a hospital bracelet, changing into the scrub top (which here, volunteers make them and BC pts all get one to wear through radiation, as they open and close with a velcro strip at the sides and down the front) and we get to keep them. A note came with it saying , do whatever you want with it once you are HEALED!! Keep it, Burn it, Bury it) and I so understand the meaning of that now), then I grab a warming blanket, then I wait my turn.
Just the process, but I will have a positive attitude and WILL get through it just like all of us here!!
So I have 8 more rounds.. as I had the one on Nov 21. 4 more whole left breast, and then 4 boosters to the anterior (so partial)
I feel good and hoping I can reach my new baseline this time and hold my breath. But if not, I’ll have to do it free breath.
I’ll send an update!! 💗
Re: Getting ready to start chemo? Join the December 2025 chemo support thread!
welp, here we are. This time last week, I was having a biopsy. KEYNOTE 522 starts Monday.
For those of you who have to drive hours for treatment and wait weeks for tests, I’m so sorry.
I guess I’ll start by saying I’m grateful to live in a terrific medical city - big med school paired with some of the best hospitals in the world. My life is infinitely easier for it today.
I’m in shock. Trying to figure out if I can work (I work in ambulatory surgery as an RN), telling everyone (my hair stylist cried when I told him), tests, tests, tests. This part is exhausting by itself
anyone else feel like they need to comfort their friends? It’s weird.
I’m buying cold mittens and socks. Got some cute hats (but it’s winter in Minnesota, so need the warm ones, too!). Gonna pack a big bottle of water and a ginger ale for chemo. And my headphones.
Oh, intro stuff. I’m turning 60 December 19. I have three kids - 37, 35, and 7. Not a typo. I have three grandkids - 6, 8, 9. We have two kitties and a dog about the size of the cats. My wife is a hospice transitions coordinator RN. I’m an endoscopy nurse - your friend from your colonoscopy.
Looking forward to meeting y’all and hanging out.
Just diagnosed - big drinker, hard job, feeling depressed
42 and diagnosed 11/7 via annual mammogram, right breast idc grade 2, ER+ 90% PR+ 80% HER 2 minus. Got an mri that showed some more things, MRI Biopsy on right for NME, all clear. Did left yesterday and awaiting results. But given Xmas cruise planned likely will not schedule surgery til new year (is that bad?).
I’m hoping for just a lumpectomy and radiation. I was a moderately big drinker. I work in big law and work is long and tough and stressful? It has not gotten less stressful.
This puts such a bummer on the holidays too.
I keep thinking when will this be over and then also..
If anyone was in similar boat - how did it all go?
Re: DCIS Stage 0 High Grade HR+
Hi@sunnywithshowers
Well, I continue with this up and down in regards to treatment.
I went on Wed, and once again they could not continue with treatment with me doing free breath.
My alignment of my sternum was straighter, as a result of a massage I had gone for. (Which I asked my team about and was told I could go)
They said, a massage normally does not affect anything but in my case, when my massage therapist worked on my collar bone, it straightened out my sternum
So, I did not have treatment on Wed, and had to go back on Thur for another CT Sim. This time I didn’t ot take a deep deep breath as the tech told me it doesn’t take much to keep the heart away.
I was such a mess on Wed, came home crying my eyes out to a very good friend over the phone and drank wine. I just need a break from being positive!!
Now with a new plan and mapping being done I am hoping to restart the week of Dec 1st.
Hello
I’ve been reading for a while and decided to join earlier in the week. I live in New Orleans , Louisiana. I, fortunately, already had a breast doctor to whom I was referred by a NP friend of mine because I have fibrocystic and dense breast. I’ve been a patient of his for almost seven years. In the beginning, I would get a mammogram and then about six months later, an ultrasound. About two years ago, I was getting annual 3-D mammograms. Results were almost always identical. All good. In early September of this year, my husband said he felt a lump in my breast. I said, it’s fine, I have lumpy breast - haha. Two days later on Saturday , September 6, 2025, while showering, I felt a huge lump on the very top of my left breast. I told my husband, I felt a lump and I’m scared. I had to wait until Monday and I called my breast doctor (who is actually a surgical oncologist - I never paid attention to that). His office had me come in immediately which was Tuesday, September 9. He is affiliated with Tulane University and he teaches medical students. I was first ushered into the mammogram room and had a very thorough mammogram. After the mammogram, I went into another room and had an ultrasound. My physician always asks if it’s okay to have students present and I’m fine with that as we have child who is an MD. As the technician was performing the ultrasound, doctor was speaking with the students, no so much so that I’d be too concerned, but I was hypersensitive to every single thing that was happening. First, the technician was going over and over the same area and taking so many pictures that I knew something was amiss. I was scared. I got dressed and my doctor had me come to his office. His demeanor was not his usual jovial self. He told me I needed to have a biopsy. He said about 95% of tumors turn out to be benign and I was scheduled for the biopsy on September 15. I went back to his office and went back to the ultrasound room and he, the technician and a student began performing the biopsy. He spoke to me about what to expect, what they were doing, punch noise, placing a clip in ancillary node and breast tumor, etc. He told me he’d be send a prescription for pain medication to CVS just in case I needed it. I got dressed and returned to his office. Again, he was somber. He’d be a lousy poker player. He told me it would take about a week or so to get the results. I looked at him and said, “you’ve been doing this for 40+ years so I know you know even without the results.” He looked down and then looked straight at me and said he was 95% sure it was a malignancy. I burst into tears and he got up and gave me a hug. I left and began the longest 10 days of my life awaiting the results. During this time, I cried a lot and tried to continue to study and complete my certifications, etc.
I am a healthcare insurance agent and Annual Enrollment Period would begin on October 15. I am licensed in eight states and chose this year to add a couple other plans to my portfolio to be able to offer my clients more options (this was before I knew about the struggle I’d be going through). I remember one morning dropping to the floor screaming and crying and I needed to get my $hit together because I had an in person training to attend that morning. My husband would be at work when I had these bad breakdowns, but I also had a lot of crying spells in front of him, too. I did get dressed and took care of business.
My husband and I went to see doctor on September 24, and I received my official diagnosis. I had IDC. It was HR-, but HER2 was pending.
I have to run, but will continue this later,
Thanks y’all!
Re: Can we have a forum for "older" people with bc?
Sorry to read the news that you will be staying around here. You deserve to take the day off.
My onco doc said that hormone negative BC is very responsive to chemo. I didn't have that much chemo, but I did have a year of Herceptin.
Done writing for a while.
mcbaker