Best Of
Re: Just diagnosed - big drinker, hard job, feeling depressed
My diagnosis and work up sounds pretty similar to yours. I was diagnosed on 10/31 and just this week found out that my second round of biopsies are not malignant. I’m back to my original plan of lumpectomy and radiation. Hopefully, I’ll get a surgery date soon. This week it’s 4 months since my initial mammogram so I’m getting pretty frustrated with the waiting. I’m very relieved but just ready to move on.
Re: CT and Lung Nodules
Hi Ladies! I have been MIA the last couple of months, but I hope you all are doing well and had a good Thanksgiving with family if possible. Looking forward to a nice Christmas as well.
Maggie15,
The changes of the insurance this year is unreal! The Medicare advantage plans in my area are also very limited, and they have once again cancelled the type of plan I am on so I have to evaluate the options. It is a big old mess right now.
I wish everyone a blessed holiday season with as much love, laughter, and family as possible.
Mourning the person I was
Watching Physical: Asia which is a competition show about people at the peak of their physical ability. It's a great show and I love it. But I found myself crying watching them realizing that I am past my peak physical self. The joint pain I have from Lupron stops me from going to the gym most days. Today included. I was a professional dancer and a marathon runner. I am so lucky to be alive right now and am so grateful. This just hurts.
Re: CT and Lung Nodules
Hi @kks_11, It's hard to know who is actually going to follow you. My hospital works on the team approach and from what I've seen they divide the workload without any real pattern, My surgeon's NP schedules my mammograms and sees me afterwards. I had been seeing a medical oncology NP until a tumor showed up in my hip and I was transferred to my MO. I've seen my RO by default a few times (he sent me to the ED when he saw my right arm.) If whomever you are seeing can't answer your questions make sure they bring in someone who can.
The lumbar puncture is part of the neuro workup. Within the past couple of months my left fingers and all toes have gone numb and my calf muscles have pins and needles. My PCP is picking the differential diagnosis of paraneoplastic syndrome (an autoimmune reaction to cancer cells.) I have gone along with the hope that the indeterminate tumor is probably benign since there is a high chance a biopsy would break break my hip but I might have to re-evaluate. Two diagnoses have been shot down so who knows what is going on.
Health insurance for next year seems to be problematical for almost everyone. My Medicare part D plan company has exited the state along with several other insurance companies. None of the seven plans left have all my meds on their formulary. Hopefully my resourceful pulmo can help with my inhaler since the $7000 it costs won't count toward my out-of-pocket limit. I hope you can get as much as possible done before the end of the year and you end up seeing a helpful provider.
maggie15
Re: Capecitabine - Side Effects
@tazzy24 Hi Michele it's nice to meet you and I'm sorry you dealing with the finger issues. I have been on Xeloda for a couple years now and it's keeping my MTNBC quiet! I am so thankful to still be on it but my hands and feet have been through it! But as I tell my MO I'm willing to"suffer" for stable! I have used many many creams you will have to find what works for you. I also limit folic acid foods.
Neutrogena Norwegian Hand Cream, Udderly Smooth, , Diclofenac topical Gel, Bag Balm. I also at times lube up my hands and feet and wear gloves and socks to let it soak in. Anyhow as Mods said check out their page and also the All about Xeloda thread. It's a great informative group who also know how to manage side effects well.
Best wishes,Andrea
Re: Can we have a forum for "older" people with bc?
marticcrn, sorry to read about your news. I hope once you have a plan in place, we can offer comfort, support and assistance. The nurse navigator should be able to assist you with getting the appointments you need for follow-up. ((HUGS))
Re: Can we have a forum for "older" people with bc?
@marticcrn Sorry to read of your dx. We are here for you so let us know if we can help.
Re: Can we have a forum for "older" people with bc?
well, dear friends, I am official. Grade 3 TNBC T3aN0. PET scan on December 18.
KEYNOTE 522 starts Monday. She will re-MRI every six weeks and if the tumor is clinically gone, I get to go to surgery (so let’s hear it for complete response) and quit chemo.
I have my heart set on DMX but I haven’t had surgery consult yet. Since I’ve lost 40 lbs (thank you Zepbound), my boobs are just loose skin with very little contents. The tumor is 5cm, so resection would be deforming and I don’t want scanxiety. I’m also terrible about getting screenings done, as evidence by the fact I missed last year’s mammo. So …
telling people has been awful. I had my manager send out an email generally saying marticcrn has breast cancer (I’m a nurse) so people wouldn’t wonder/talk. My hair stylist cried when I told him. I haven’t told my adult kids yet and my 7 year old just knows Mommy had a lump tested. Gonna get there later this week. I really hadn’t anticipated how bad telling people would be.
Port soonish, but chemo starts first. I need your nail care tips, your skin and stomatitis tips. Alll the hints pls.
Hugs to you all.

