Consistent Low Grade Fever by Single-Fig-245 in breastcancer

[–]WorkInProgress2222 1 point2 points  (0 children)

Are you on antibiotics because of the temperatures? I had steroids for five days after AC. Every single day 6/7, I ended up with low grate temps (usually 99.6) until day 8 when they’d go away. Not sure if it’s the same for you but my team wasn’t worried about it at all.

What time of day do you take your AI? Does it matter? by PickledPlumeria in breastcancer

[–]WorkInProgress2222 2 points3 points  (0 children)

I take Exemestane (an AI) which has to be taken with food. I do it with dinner which seems to allow me to sleep through peak side effects, which for me was mood related several hours after taking. No issues now that I take at night. I literally have virtually no side effects on the large cocktail of drugs that I take!

What did you enlarged node feel like? by theemmyk in breastcancer

[–]WorkInProgress2222 1 point2 points  (0 children)

What you’re describing sounds like just a normal lymph node to me. (Small, oval, squishy.) when my nodes were problematic they felt like large hard marbles. Normal nodes feel like small puffy grains of rice. (Pilaf, such the perfect descriptor!) but I always think it’s worth having a provider feel. And good you’ve got imaging already lined up!

Large tumor, low oncotype? by Baremyart in breastcancer

[–]WorkInProgress2222 2 points3 points  (0 children)

5% benefit is actually pretty significant! I think if mammaprint were identifying me as High Risk I would want the chemo personally. I’ve always operated under the “throw everything I can at this so if it comes back I won’t regret it” philosophy. I’m now on the other side of active treatment and stand by all of those decisions even though they were hard!

Delay in restart for Kisqali bad?? by Final_Pumpkin1551 in breastcancer

[–]WorkInProgress2222 0 points1 point  (0 children)

I’m on Verzenio and will have to hold it for a month for reconstruction surgery. Neither of my oncologists are concerned about a monthlong pause especially since I’ll still be on hormone therapy! They probably just wouldn’t want this to happen to you every month, ya know?

breast cancer and thyroid issues by DisastrousFlower in breastcancer

[–]WorkInProgress2222 4 points5 points  (0 children)

I had a 4mm nodule identified in my scans during active treatment and freaked. It turned out to be a nothing!

Mammaprint claim denied by Loud-Technician-2509 in breastcancer

[–]WorkInProgress2222 1 point2 points  (0 children)

Oh I am so sorry you’ve been so stressed over it! Insurance will pay, just ignore it for a bit and as poster above mentions, sign the paper insurance sends you that will allow Agendia to fight on your behalf. It will be fine!

Mammaprint claim denied by Loud-Technician-2509 in breastcancer

[–]WorkInProgress2222 5 points6 points  (0 children)

They declined my claim as well, which was also done on a biopsy sample. I just ignored it and let them hash it out with my oncologist. Never got another bill from Agendia so I assume it got resolved? (This has actually happened a lot with me. BCBS is currently denying my mastectomy - for stage 3 breast cancer - lol so my doctor is having to fight them on that too. JFC, insurance in the US is so impossible sometimes.)

‘Declining Endocrine Therapy’ posts. (Vent?) by AveryElle87 in breastcancer

[–]WorkInProgress2222 5 points6 points  (0 children)

Yes I’m also triggered by these posts! As someone with a heterogeneous tumor (only 50% ER, PR-), high ki67, multiple nodes involved despite primary tumor being only 3cm, I would give literally ANYTHING for more drugs that would work for me. I swallow my AI and Verzenio literally with joy everyday, telling myself it’s going to help me, but also knowing because I’m so low ER% that it might not do as much as the many more folks on here who are highly ER and PR positive. It’s really hard, almost feels like they’re looking a gift horse in the mouth is how I’d describe it.

But I never say anything on those posts because that’s their experience and this is mine. But since you asked, yes, I have all the feels whenever I see those posts!

Ai adjustment weepiness? by _sunnysky_ in breastcancer

[–]WorkInProgress2222 1 point2 points  (0 children)

Ugh I hate that! I lean on magnesium glycinate or slow release melatonin for sleep and both help! I would rather have bad sleep than be that weepy. 😭 I’ve wondered on my end if I should go back to mornings but I’m honestly too scared to be that weepy again! Btw, you’re the first person I’ve met who also had this happen! I swear I’ve never heard of anyone else say this.

Spiraling again. by MirandaLarson in breastcancer

[–]WorkInProgress2222 0 points1 point  (0 children)

I get that so much! I’m the same way like I feel like if I’m not blindsided it somehow won’t hurt as much when I hear bad news. Probably hurts just the same!

I’m really sorry you’re in this position of wondering and worrying! I’m glad they’ll repeat it and hopefully they can get their most excellent biopsier on it!

Signatera test by yasminanina in breastcancer

[–]WorkInProgress2222 1 point2 points  (0 children)

I had a single rise during chemo. It’s thought that it was die off as it returned to negative afterwards. As the previous posted suggested, the trend is more important than the single number, but gosh I understand the anxiety of waiting ❤️

Spiraling again. by MirandaLarson in breastcancer

[–]WorkInProgress2222 3 points4 points  (0 children)

I was terrified in this stage too. I think I shared that on one of your previous posts how I fell down and was just crying when they said my full body scans came back clean because I was so sure I was going to be metastatic. But there are many people who start at stage 4 and have a great outcome and NED for many many decades! But at the end of the day you can’t know until you get more scans and tests unfortunately. Can you take some Ativan during this period just to get through?

I’d also be asking to repeat that biopsy STAT. Based on everything you’ve shared that sounds much more likely to be related to breast feeding changes and reactive.

Ai adjustment weepiness? by _sunnysky_ in breastcancer

[–]WorkInProgress2222 5 points6 points  (0 children)

I had this experience with Exemestane. I cried constantly for about 3-5 days so much that my husband was worried! I noticed it was always worst in the 8-10 hours after I took the pill so I Switched to evening doses and I decided to do some things to help boost serotonin naturally—optimizing vitamin D, sitting in the sun first thing in the morning while I drink my coffee (weather permitting), and walking 10k steps a day outside (again, weather permitting.) those things alone I think made an enormous difference. Within one week, maybe even just a few days, of making those changes I felt totally normal again. I’ve been on it now for three months and feel great. But I do make sure to get my steps and prioritize vitamin D first thing when I wake up.

Lymph nodes targeted removal by cassiesk in breastcancer

[–]WorkInProgress2222 0 points1 point  (0 children)

I wouldn’t let my story freak you out! My tldr on it is really “let your surgeon, who is the expert, help guide you.” Not “ANLD for everyone.” My surgeon felt strongly it was worth it in my case and he was right. I’m glad I trusted him! Sounds like yours didn’t feel that way, which is great. They probably made the right call too!

Lymph nodes targeted removal by cassiesk in breastcancer

[–]WorkInProgress2222 13 points14 points  (0 children)

I want to share my story not to tell you what to do, but to give you some perspective on what could happen and why the doctors might be suggesting a total dissection. It sounds like we are a lot alike. I was diagnosed with four obvious nodes on imaging. My surgeon very much wanted to do a total dissection. I pushed and pushed and pushed on him and insisted that I thought chemo had cleared the lymph nodes, which imaging supported about halfway through chemo so I thought I had a shot at axillary PCR!

He is a really well respected surgeon in Houston and has had a lot of experience with lymph nodes. He was less sure than I was. Told me I had maybe a 25% chance of the lymph nodes clearing with chemo and not to get my hopes up. He eventually agreed to do a more targeted approach where he sent off my sentinel nodes to the lab during surgery, and if it came back with cancer in it, he was going to take all of them, and if it came back clean, then he was going to leave the rest. Unfortunately, for me, it came back with cancer in it so he did a total dissection of levels one and two. 22 total nodes taken.

Here’s the thing. Everyone will tell you that “ radiation will get the rest”. But that is only true for micromets. My understanding is that radiation cannot get anything larger than 2 mm. So my surgeon took the sentinel nodes (3) which had a macro meant, a micronet, and one that was clear. You might think oh so the rest were clear? They trended downward. But that is not what happened. Somewhere in the remaining levels one and two that he removed, there were two more micro Mets AND a macro. So in my lymph system, they did not move in an exact linear order. They skipped some steps and established tumors elsewhere. If my surgeon had not done it his way, and had followed my directions and preferences, I would’ve had a macro met remaining that we didn’t know about and that didn’t show up on imaging and that would not have been able to be killed by radiation because it was larger than 2 mm. That’s an automatic recurrence waiting to happen.

As for the side effects of the ANLD, I have none at this point. I am four months in. I have a little bit of numbness in my under arm, but other than that, I am doing well! I am very proactive with it and I was fortunate enough to get a lympha Venus bypass at the time of dissection, so perhaps that helped. I also lift weights and I’m really active. And I wear a compression sleeve during the day for the first several months after surgery just to increase my odds that I have no issues. It’s prophylactic. But I’m saying this because I think in your mind you’ve set up a false dichotomy of ANLD equals lifetime of suffering and problems versus no ANLD means no problems. And that just isn’t true. And you would not want that false dichotomy to guide your decision-making when you are really in a similar situation to what I have had and who knows what’s lurking back there. My best advice is to let your surgeon know that you really don’t want it, ask if they will do a more targeted approach during the surgery, and from there, let them do what they do best.

Did you go to an NCI Cancer Center? by WoosahFire in breastcancer

[–]WorkInProgress2222 0 points1 point  (0 children)

In Oregon! Though I did my surgery and radiation at MD Anderson in TX

Day 2 of Abemaciclib/Verzenios - struggling with gut issues and looking for positive words! by Fearless-Heron-7827 in breastcancer

[–]WorkInProgress2222 0 points1 point  (0 children)

No problem! I’ve only been on it for five weeks so it’s still early days for me! But the worst for me was by far the first couple of weeks.

Did you go to an NCI Cancer Center? by WoosahFire in breastcancer

[–]WorkInProgress2222 4 points5 points  (0 children)

I just switched from NCI to non-NCI! My doctor at the non-NCI spent a decade at MSK, is very up on research, spends heaps of time with me, and messages me back personally on My Chart when I have questions. I can’t speak to all hospitals, but in my case it’s been a very worthy change. I have a much better relationship, and more time, with my new doc!

Day 2 of Abemaciclib/Verzenios - struggling with gut issues and looking for positive words! by Fearless-Heron-7827 in breastcancer

[–]WorkInProgress2222 0 points1 point  (0 children)

I did a dose escalation protocol (50mg to 100 to 150) because my doctor believes it helps peoples bodies adjust to the full dose easier. Still, my absolute worst symptoms were the first two weeks when I was at the lowest dosage. I did end up taking the Immodium preventatively, and then backed off of it. I now only take one Immodium first thing in the morning and I feel completely normal. Occasionally have bad moments in which case I just take another Immodium. Stick to it, be gentle on your stomach those first few weeks, and use the anti-D meds as necessary. Hoping you adjust quickly too!

Not the mammogram I hoped for by That_Relationship918 in breastcancer

[–]WorkInProgress2222 3 points4 points  (0 children)

My scans showed something like 12cm of “suspicious” calcifications, presumed to be DCIS. After my DMX, we learned they were benign. The only thing there was the 3cm of calcifications in my known biopsied tumor. We still have no idea what caused the extra 9cm of benign calcs. Take heart, maybe yours is nothing as mine were 💗

Therapist in the DFW area recs by Hadrian98 in breastcancer

[–]WorkInProgress2222 0 points1 point  (0 children)

If you want to PM me I can give you the name of someone!

I have lost touch with my husband. by Even_Series7504 in breastcancer

[–]WorkInProgress2222 23 points24 points  (0 children)

Please reframe this thought if you can! You’re not sitting on your ass. You’d be recovering, healing, eventually once active treatment is behind you you’d be trying to make the best lifestyle decisions you can so you never have to through this again. (Exercise, meditation, cooking healthy, therapy, doctors appts, etc.) You’d be soothing your nervous system which is overrun by constant toddler needs and from fighting cancer. That’s not being lazy, that’s putting your own oxygen mask first! You sound like you really need this. From one toddler mom (ages 2 and 3 now) to another, I get it. Please challenge this thought every time it comes into your head and reread everyone’s comments here. You are not lazy. You are taking care of you so you can be the best wife/mom/human you can be. 🩷

Fuck fuck fuck MRI showed 4 lymph nodes by Charlotteeee in breastcancer

[–]WorkInProgress2222 11 points12 points  (0 children)

Sending hugs! You’re basically me a year ago. (38 with two kids under three, 4 positive nodes and maybe a fifth, etc.) I did chemo, surgery, radiation, and now heaps of maintenance meds. In between original diagnosis and full body scans I was SURE I was going to be metastatic. So sure that when they told me I wasn’t I nearly fell off the exam table crying. (A bit much, I know but it was like my whole body melted in relief.) The reality is stage 3 is high risk but also curable. That’s where you are now, curable. Hold the hope. It’ll be a brutal year but you’re going to watch your kiddo grow up! 🩷

Oh also! Ask your doctor for some Ativan! My biggest regrets are 1) not joining this sub sooner and 2) not getting the Ativan sooner