Wife Just Diagnosed w/ ES SCLC - What Can We Expect?
My wife received the following diagnosis yesterday: Primary malignant neoplasm of lung, secondary malignant neoplasm of liver, secondary malignant neoplasm of vertebral column. Four months ago she had a chest x-ray performed and no anomalies were noted.
We have surmised that this is likely Extensive Stage Small Cell Lung Cancer.
She has been referred to a local oncologist and a PET-CT scan has been ordered by our doctor.
Last evening we requested an appointment at the Mayo Clinic - Jacksonville at the suggestion of a friend.
Can anyone tell us what we can expect over the next few days/weeks/months?
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Morning, Bob-It sounds as if you had a productive day, accomplishing all the steps that need to take place prior to treatments. There are some wonderful services out there and I'm glad that you are taking advantage of them. Hospice is incredible and will ensure Liz's comfort. You can ask them anything and they will bend over backward to help!
I don't know why pharmacists (probably insurance co's as well) don't put when you should take medications...it's so easy to mistake directions. At least it was for only a few nights! Now you can get some good rest, I hope.
Please extend my best to Liz and please take care of yourself. It was a big day yesterday and I bet you both need some well-earned rest!
I'm here if you need a prop, shoulder, or anything. I hope that you will take advantage of this!
Great job being proactive. I took care of my mom and that is what I learned. Speak up and make sure you have a great list of questions and a journal for doctor’s appointments. Praying for your wife and your family🙏🏼
Bob- Two pairs of eyes are better than one, so if you need additional support as a caretaker you might want to at least glance at Connect's caretaker support group
https://connect.mayoclinic.org/discussion/meet-fellow-caregivers-introduce-yourself/?pg=24#comment-112259
Enjoy your Sunday. Merry
Thanks Merry, Liz has a physical therapist and a nurse who checks up on her once a week.
The biopsy confirmed Non-Small Cell Lung Cancer and they will be going after the lesions in her brain first with 2 weeks of radiation treatment and then the cancer in the remaining organs with chemo. The oncologist will be DNA/Genome testing the cancer to see if Liz qualifies for targeted treatment versus generic chemo. We have been waiting on Insurance approval since Monday to start the treatments and I will be calling the insurance company tomorrow to see what the hold up has been....... Should be a no-brainer......
Good morning. Ah, an answer! And a way forward. Does this preclude other cancers (pancreatic)? My fingers are crossed that you learn that her treatments are approved when you call.
How is Liz feeling? How are her spirits?
I’m glad to hear that things are moving along, and that at least you know some of what to expect. Is there a time line for the DNA/biomarker test results? The sooner the better, as a targeted therapy can really be a game changer. Take care!, Lisa
Liz's spirits are good and her appetite has been better since she started the steroids'. Unfortunately our insurance provider uses a third party to determine whether certain procedures are necessary (PET Scan, Radiation Treatment) and they have been in disagreement with the 3rd party on who will make the call on Liz's radiation treatment since Monday. In a nutshell, we have lost this week to bureaucratic B.S. and are hoping an approval to treat will be made NEXT Monday. If the Radiologist gets the approval Monday, Liz will begin treatment next Wednesday.
They will be doing the DNA/Biomarker testing during the two weeks of initial radiation treatment for her brain lesions. The Oncologist told us that interestingly people from the South do not generally have DNA specific NSCLC whereas folks from the east/west coast generally do. Have not researched this, but he also said that this will not prevent him from ordering the Garden 360 and other DNA tests anyway.....
Bob- I would love to hear what resource this information came from about DNA/biomarker specific for NSCLC being divided by sections of the country. With so much mobility how could anyone have tested this to date? I couldn't find such a fact on Snopes or Wikipedia.
Does this even make any sense to you?
In my completely non-scientific observations, this isn’t the case. I’m glad the oncologist has ordered the biomarker test, it really is standard of care in the US although insurance companies like to deny claims for that too. It should be done as soon as possible, weeks ago in my opinion.
Diagnosis is such a difficult time for patients and caregivers! It’s completely consuming and while it may not seem like it, it does get easier, hang in there. Thinking of you and Liz, and I’m glad she’s starting to feel a bit better.