Small Cell Lung Cancer: Let's connect

Thank you Coleen for connecting us to the right group. These past two days have been a whirlwind of just confirming Pop’s primary tumor in his upper right lung ,yesterday from his PET scan results done on Monday. He was diagnosed December 18th with secondary liver cancer after having a Biopsy. The soonest we could be scheduled for a PET scan was January 6th.
After We received his Biopsy report on Monday ,I freaked out after doing some research. His Pathologist from the Biopsy concluded his liver tumor was a high grade neuroendocrine carcinoma, consistent with small cell. I sent the Biopsy report to a friend and other pathologist ,who recommended he see a neuroendocrine specialist at Moffitt, here in Tampa where we live. March 17th was the soonest Moffitt could schedule him with the Neuroendocrine oncologist. I told them that we needed to be seen sooner so they suggested he see aThoracic specialist. We have a January 22nd appointment with the Thoracic specialist. So you see, we are just getting started on this roller coaster ride. Any information and help is greatly appreciated.

u.w. Madison has some great new machines, they have 1- of 3 in the world no chemo  radiation machines and a pet program that is one of the best in usa

i  just finished 5 lazier radiation treatments for lung cancer. in Madison U.W. HOSPITALthey found a cancer the size of my thumb nail.THEY HAVE 1 OF 3 ADVANCED RADIATION MACHINES IN THE WORLD. 1-IN JAPAN 1- IN LAS VEGES, AND 1- IN MADISON. this is the place to go, they are the best in the world.  after 5 treatments and 3 months later a xray shows my cancer shrinking and all gone-thank god.  those  are my only choice for this kind of cancer. hope i helped you with your husbands problem, i have also has prostate cancer , fixed w/ seeds in Sarasota fl. good luck,

Thank you so much for sharing your story. My husband has just been diagnosed with small cell cancer in his right lung and liver cancer. Once we have a plan of attack, I will review your medications to see if they treat him with any of the same ones. I have not read good things about Keytruda but you would know more about how it worked for you. Wishing you well will your follow up on the 27th.🙏🏻

I was d diagnosed with stage 4 Malignant Neoplasm Of Lung Adenocarcinorm in the right Lung, Nodules in liver and stomach. The right lung had huge Timor which had fluid in lining of lung. All cancerous. At the Mayo in Rochester they did scans and had to remove a quart of guild for breathing before they could start on how to treat after 5 days and seeing different options. Surgery and radiation was ruled out as was the once a month pill. I was put on Carboplatin, Pemetrexed, Pembrolieumab and Keytruda Immune therapy every 21 days.the 3 chemo tram eats shrunk the tumor almost in half and nodules have stayed stable. I got very sick for 4-7 days on the chemo treatments which took days to get back strength than back for another dose.April thru September than went on just the Keytruda. Had my last treatment 6th of January and on 27Th will have scan done to see what my next step will be. This is not beatable so I believe I will go for quality rather than quantity of life I’ve had left.
This diagnoses was a shock as i played pickle ball 5 days a week two hours and was active in swimming and walking and everyday chores. The first sigh of trouble when silvery meals on wheels I walked up three flights of stairs and couldn’t breath when got to top. Called my primary Dr who had me come in as I taught I had pleurisy. After X-ray, scan and blood work same day was told I had cancer and what was my choice. Biopsy had to be done and here at St. Cloud hospital (only place to have done) and couldn’t get me in for 3 weeks. Decided to go to Mayo and they had me in 3-4 days. They have been amazing. Trouble was driving 3 1/2 hours one way for treatments and if blood work wasn’t up to par would have to go home and reschedule.so know am getting treatments at the cancer center here in St Cloud. Back to Mayo every 3 months. Sorry about long post!
Colleen
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@popkorhn- Welcome to Mayo Connect. How awful for you and your husband, as if one cancer isn't enough. I am a mentor for Mayo Connect Lung cancer group. Hearing that "you" have cancer is true shocker. Have his doctors discussed any treatments as yet? How is he feeling physically?
Here is some information about lung cancer spreads to the liver, which is very common.: https://www.verywellhealth.com/lung-cancer-spread-to-the-liver-2249263
I'd also like to ask how you are doing? Connect has a separate group for care givers which I think will help you immensely. You will need to take care of yourself as well and I hope that the love and caring that other caregivers share will help you too. https://connect.mayoclinic.org/group/caregivers/
I'd also like to invite @margot69 @lady1lake @cheris to join this conversation.
Please continue to reach out on this site so that we can continue to support you. Would your husband want to join us do you think?

Hi @popkorhn (fun name), welcome to Connect. You'll notice that I moved your post to the Small Cell Lung Cancer discussion. I did this so that you can more easily connect with others living with SCLC like @margot69 @lady1lake @cheris and others.

What treatment is your husband on or had? How is he doing? How are you doing?

My husband was just diagnosed with small cell lung cancer which has spread to his liver. Any information from anyone who has survived this would greatly be appreciated.

@lady1lake- Good morning. Please keep us updated on your progress!

Thank you @merpreb. This Mayo connection means the world to me. I do not discuss my cancer problems with many people, mainly just my family & a couple of very close friends, who have also had cancer.
I am feeling very positive because like the other 3 different cancers I have had over the past 17 years, all were caught in early stages. But, have to admit since this one is so close to the brain it is a bit more scary. Am having headaches, just not as bad as before the targeted radiation treatments. Of course pain meds do help. I know that the brain cannot feel pain, but the scalp, bone & blood vessels surrounding the brain are sensitive to pain.
Thank you all for your kind, caring thoughts & prayers.