Best Of
Re: Can we have a forum for "older" people with bc?
Surgery was completed and I was out the door by 9 AM. We went to CVS to pick up two scripts. Home at 10 I took one hydrocodone and one ondansetron- anti nausea. Exhausted but couldn’t sleep, closed my eyes for a while but waste of time.
Nurse called from surgical center to see how I was doing around 5 PM. I told her I was good, and asked about the anti nausea med. She said some people feel nauseous on hydro. I don’t have to take it, I feel fine on hydro.
I’m in a lovely Velcro shoe, picture coming. And using a walker for 5 days. The shoe I believe stays on for 4 weeks. Follow up is 7/2, and most likely 7/14-16 I’ll see them again to be released.
Just took 1 more hydro. I’m sticking to 1 every 6 hrs, vs what I could take is 2 every 4 hours. I don’t want to jinx myself, but I’ve had bunion surgery 3x. On a pain scale level, this is a cake walk.
Vacuum lines on my carpet are thanks to the robot vacuum. Haha! When we came back home my partner set it off. This is the Shark, it doesn’t map your rooms, so I call this one Willy Nilly.
I’ll report tomorrow if I still think it’s a cake walk. Fingers crossed.
Re: I say YES. YOU say NO....Numero Tre! Enjoy!
I read that of the other couple the man is in critical condition. This is what is passing for a president. He and everyone in his government is just place holders/vile as the day is long.
Re: Lung Nodule Incidental Finding
Update - the nodule size estimated on PET to be closer to 1 cm, flat appearance, MINIMAL uptake and in a location most likely to be an intrapulmonary lymph node. My BC team feels it is most likely that or something else benign.
But scans always seem to lead to more scans! Some diffuse uptake showed in my vaginal area which they presumed was urine contamination. I did drink a ton of water prior and had to pee twice before procedure and again right afterwards. The report recommended a clinical followup so that is what happened yesterday despite just seeing an OB/GYN 6 weeks ago with normal screening test results. I have now been visually and manually inspected again. The gynecologist said my vagina has an A+. 🤣
A 1.4 cm thyroid nodule was found so off to an u/s for that. 🙄
Pulmonologist scheduled 3 months CT followup for lung nodule. She also ordered a urine test for lung fungus and a blood test to check for lung cancer. Those results are expected to be negative but of course I will exhale completely when the results are returned in a week or so.
I have now decided to forgo scans unless ABSOLUTELY necessary. My LDL numbers were high, but nothing else indicated a need for a cardiac scan. My score was a perfect 0 for arterial calcium blockage.
And the incidental lung nodule has resulted in a cascade of followups, more scans, appointments, tests, anxieties, worry, and medical PTSD.
In fact, I spent the 12th anniversary of my initial diagnosis at the pulmonologist.
I literally have had more appointments this week and in the future from this one incidental finding than I had during my initial cancer diagnosis journey.
I am grateful for my docs - my oncologist, who dismissed me 7 years ago, expedited my PET scan. My breast surgeon was able to preview the PET report and interpret it as being "NOT very worrisome" and "good news." All my docs and the radiologists who have read my scans are doing their due diligence and leaving no stone unturned.
And, if by some chance, the lung nodule turns out to be a very small primary lung cancer, well, good, it's been found and can be removed with very good projected survival rates when this small.
But I can't help but think that this all could have been avoided by my turning down a less-than-necessary scan!
Re: Dealing with Lymphedema w/o surgery?
@pemala im so sorry to read of your continued suffering. I hope you can find some relief as well. My swelling was not severe, and the Velcro wrap, called a Circaide Recovery banadage worked well for the two months I needed it. I now wear a compression sleeve , and since my insurance covered it, I also use a pneumatic pump which is a massager and that keeps the swelling in check. But I did not experience pain. In your pockets with support ❤️. Wishing you free of future suffering.
@maggie15 i love how ingenious you are. Love how you figured out that the red light therapy was an option to try , and so glad that worked for your DH. I’m so sorry to read of all the radiation complications you have endured. I cannot imagine the stamina it has taken to move forward. And yet, here you are. Loving and caring and sharing. ❤️
Re: Dealing with Lymphedema w/o surgery?
My husband had an arm like yours when severe LE developed post surgery for a complicated elbow break. His super swollen arm just hung there like a useless appendage; he had no feeling in it. He couldn't even attempt the prescribed physical therapy. The surgeon and PT had no ideal what to do so I came up with possible veterinary solutions since I have some background there and propsed pulsed magnetic therapy, ultrasound and photobiomodulation (red light therapy.) Ultrasound is used on humans in ortho but the doctor nixed it since it would heat the metal hardware. A fellow in the group had seen red light therapy used in neurological units when he did his residency so we tried that. It actually worked well and he was able to start the 18 month process of getting the use of his arm back. The plug in wraps are expensive but you might be able to borrow one or find someone who provides treatment with them. The animal ones work just like those for humans. The other therapies might work for you since you don't have metal in your arm. The cause of your LE is different but that shot in the dark worked for him.
Your statment about SEs being worse than the cancer itself is so true. My cancer was only stage 2 and radiation injured my lungs, thyroid, esophagus, trachea, nerves and now possibly liver (biopsy pending.) The brachial plexopathy is slowly advancing in my right arm. I'm hoping I never get to the stage where it doesn't work at all. Maybe a nerve block would help your pain. I had one done for intercostal nerves since breathing was excruciating; it still helped when it wore off six weeks later. I hope you can get some relief.
Re: Dealing with Lymphedema w/o surgery?
A quick update: Curiously, the arm pain from swelling and the swelling itself is creating the worst impact on my quality of life: My arm doesn't work = bandaging and putting on clothes is really difficult, as are a lot of things now; the opioids don't seem to numb the pain; people who see the swollen arm get really disturbed.
Who would have thought a side effect of cancer could be worse than the cancer itself? ;)
A smooth journey to all.
pemala



