Best Of
Re: Can we have a forum for "older" people with bc?
petite1, glad you were able to enjoy your new hideaway. I am sure it is lovely this time of the year. Have you taken Midnight Louie yet?
Chris, you really know your show characters. Hope your thumb is improving.
Sandy, the end of boxes seems to be in sight. Once you are back living in the house, you'll find you will still be making decisions about where things fit best, what stays and what goes and what decor you'll finalize. I think we all tend to "save" the good stuff for later use and then realize this might be later at some point.
cindyny, hope you enjoyed the dinner and the play.
Was able to pickup oximeter I need for overnight sleep study. Have been waiting since May for this to happen. They did contact me the day before I was leaving for the cruise.
Needed to go to CVS for the prescriptions ordered by pain management. I was surprised that Medicare paid for the real Lidocaine patches and not the generics. I must have reached some kind of threshold in my prescription plan because the last one I picked up plus today's was free.
Yesterday my back was very tender all day but the spasms were silent until 11pm. I had a really rough night as a result even taking a Tizanidine. Spent most of the night trying to find a comfortable position.
Today was overcast and then the rain came. It is to persist into tomorrow. I have chest CT and then I am done until I get my flu shot on 10/5.
Hope everyone had a great day. Waving "hi" to everyone.
Re: CT and Lung Nodules
Marge, I’m glad the smaller granuloma was the nodule of concern. From what I have read the monarchE trial showed that two years of verzenio continues to provide good protection even after it is stopped. You’ll still be taking tamoxifen and your MO will continue to monitor you. Long term use of verzenio is more likely to cause side effects like blood clots, ILD and liver problems. I’m dealing with those lung problems from rads and high liver enzymes from a statin. The malfunctioning liver caused a rare neurological syndrome so my right hand and arm is numb and won’t work; hopefully another year or two of PT will bring it back per my neurologist.
It must feel like your security blanket has been taken away but I wouldn’t wish SEs like these on anyone. Breast cancer upends our previous lives. Ask your MO for a referral to a counselor who can help you talk through your fears which are real. Hugs for you.
Re: CT and Lung Nodules
Went to the dr today. He said the granular is the nodual and there no need to do CT any more but I will be asking again in a year. He also took me off my verzenio and I am really scared. I feel like I am lossing my protection. He didn’t realize I been on it a 2.5 years. I should have been off at 2 years. I don’t know how to deal with this mentally.
Re: So...whats for dinner?
Not sure if Kimmel was being aired here, but I tried to tape it so I could hear what his comments were.
My family always ate differently (we are from Europe) so as a kid, I learned to love calf's brain, kidneys, hearts, blah, blah…I introduced DH to lamb and he loves it. Also, goat.
I think peanut noodles tonight. DH's (yet again a new onco) appointment today to see what options we have for his rising PSA again. HATE this so much.
Re: Can we have a forum for "older" people with bc?
Sandy - congratulations on making significant progress with the move back in. My head is spinning thinking of all you are handling. How much longer will you be in Lincolnwood? Happy to hear your HK will be returning next week to help.
Cindy - thinking of you and hoping today’s oral surgery visit went as well as can be expected.
Betrayal - I’m so sorry to hear the back spasms are still an issue. That really limits one’s activities. I hope the lidocaine patches offer relief. Good luck with the chest CT. Do you have another trip coming up? I’ll hope the back issues are resolved by that time.
My MRI/MRCP indicated the pancreatic cyst is stable. I’ll have another one in a year and then the GI doc will decide if I can go to having one every other year for the next 10 years. I’ll get the Covid and flu shots next month.
We signed a contract to have our pool removed. It will take the contractor a few weeks to have the permit pulled because our city likes to drag their feet. Apparently the city decides the cost of the permit on a case by case basis. Such a deal! Once the permit is pulled the contractor will schedule the pool removal. The goal is to have it done by Thanksgiving when we leave for Spain.
We officially pulled the trigger on the trip to Vietnam next March. My thought is this will be our last big trip as we are getting older and travel is expensive. I’m doing all the planning as I prefer to have control of the itinerary rather than have a TA tell me what to do. Basically I’m a bit of a control freak 🤷♀️ with travel. The airfare and hotels are booked. I can wait a few months to book tours which I will mostly do through the hotels. I did book business class airfare due to the distance we are travelling. While we’ve flown biz class previously I’ve always used miles if it’s personal travel or flown on my employer’s dime for business functions. I’m retired and out of miles so I found a decent fare and purchased it yesterday.
Waving hello to all.🙋♀️🙋♀️🙋♀️
Re: 2017 BC Diagnosis…how are you doing?
The FES PET was approved in 2021 and can be useful for detecting ER+ cancer, especially lobular which has weak FDG signals. It is three times the cost of a FDG PET ($24,000 vs $8,000) so will only be covered by insurance if the doctor can make a compelling case for it. There are currently only 43 hospitals which do them. If you are taking tamoxifen or fulvestrant you need to go through a 6 month washout first. AIs don't interfere. As crossh said the FES doesn't show mets in the liver, intestines or deep in large bones.
It took 9 months from my MO's referral to ortho for hip pain to getting a FES PET for a tumor in my acetabulum which looks like a met on MRI but can't be biopsied without irreparably breaking my hip. They were looking for something else ER+ to biopsy but only my right lung lit up; that was my radiation induced pulmonary fibrosis which I learned has estrogen receptors. I'm choosing the ability to walk, hoping the bone doesn't crack and being optimistic that this tumor happens to be one of the 5% in this location that are benign. I've had so many rare SEs from radiation scatter that I have quit worrying and just deal with whatever weird health problems show up.
Crossh, I hope your surgery, chemo and radiation go well. It's nothing anyone would choose to do but we don't have much input into what goes wrong healthwise. As Sandy said cascading side effects lead to more medical problems to deal with.
Re: I WANT MY MOJO BACK!
I agree with laughinggull! I am not on aromatase inh, all I did for my treatment was surgery. I chose not to go on meds or have radiation….but I am having scans every 6 mo. So far all is well. My MO is supportive of taking bioidentical hormones. I use Testoterone cream, progesterone pill daily (all bioidentical). And I use estrodiol patches twice weekly. Again, bioidentical. I would change MO to someone who understands the new info on bioidentical hormones…there are many MO's now I think who would agree with my MO.
Blessings!