Living with lung cancer - Introduce yourself & come say hi
Welcome to the Lung Cancer group on Mayo Clinic Connect.
This is a welcoming, safe place where you can meet people living with lung cancer or caring for someone with lung cancer. Let's learn from each other and share stories about living well with cancer, coping with the challenges and offering tips.
I'm Colleen, and I'm the moderator of this group, and Community Director of Connect. Chances are you'll to be greeted by volunteer patient Mentors and fellow members when you post to this group. Learn more about Moderators and Mentors on Connect.
We look forward to welcoming you and introducing you to other members. Feel free to browse the topics or start a new one.
Let's chat. Why not start by introducing yourself?
Interested in more discussions like this? Go to the Lung Cancer Support Group.
Thanks Colleen
We have found the report on our chart on the web and are excited to know she is much improved!
The tumor has shrunk, etc.
Here our discussion items for the doctor tomorrow:
The report is encouraging, and we are cautiously optimistic. We do have the following concerns to discuss with you tomorrow:
- Where is the tumor/s located currently?
- Are there new tumors or new changes?
- Restaging - Am I still considered Stage IV?
- Have you ever gotten a lung cancer patient to "remission"??
- "Benign flow related enhancement in right lobe of the liver"? Does this need further study?
- How long can I stay on the infusions?
- Should I now consider a port?
- Would you please send an update with the latest scans to dr Menefee at Mayo?
- Any suggestions about exercise?
- Heart monitoring since that is one of the supposed side effects of the herceptin/perjeta doublet. How close must we be monitoring it and methodology?
Colleen:
Thank you for posting this information. Additional app Improvements along with breathing games will be launched soon!
Hopefully we can encourage people to take time out by learning how breath deep! It has helped me sleep all night, walk & run, and climb higher. It just takes practice and time.
Hugs
Linda
Dear burrkay:Thank you oir your kind words. I hear about lung tragedy too often. My journey with lung cancer has taught me that researchers everywhere...even at Mayo Clinic researchers desperately need research funding, to find the best ways to properly diagnose and properly treat lung cancer .My life's passion is to introduce people of all ages to their Lungs with more fun facts as well as lung health and cancer facts. I have seen amazing growth in research and treatment since my 2008 surgery, but mute needs to be done, would you agree?I would enjoy meeting you and talking with you more about possibly speaking in your community. What do you have in mind?Thanks so muchHugs for caringLinda
Burrkay:You will both be in my thoughts !All my bestLinda
That's a superb list of questions for the oncologist tomorrow @burrkay. I cant think of anything to add except perhaps: what are the next steps?
I look forward to hearing how the appointment goes.
Thamks for taking the time to update us @shortshot especially when you have multiple health concerns to contend with.
We have several members on Connect talking about stage 3 kidney disease as well as people managing life with a pacemaker. Let me know if you'd like to be connected to those discussions.
Windwalker (: what a wonderful "handle"! My church is mostly my support. zzi. I enjoy my Sunday church. I was also gong to Bible study, but I get awful tired. I have been married 66 years. My husband has his own health problems. He has a permanent foly, and has asbestosis. I am in somewhat better shape than hie is, but not much. Doing some kidney things too. I have third stage kidney disease.
Going to have a cat scan in couple weeks, and also my lungs cat scan. Our oldest son lives with us and does the driving for us. Me... I get up every day feeling good or not and get dressed, fix some kind of breakfast for us. Keep thinking I will get my book done, but don'seem to get it started. Been thinking of this for at least 40 years. I live on the oregon coast in Pacific Citiy. This is a small fishing town. Used to help myhubby commercial fish in a Dory. It is a 22 foot flat bottom boat that we used to slide off a tilting trailer into the ocean. I was one of five ladies that did this in 1971. I enjoyed the fishing, boat ride too in the ocean.We fished from 1971 to 1995. Even tho I did most of the cleaning of the fish, I had fun. We (both) had jobs in Portland, so come Friday we would drive down about 80 miles, and fish for the weekend (weather permitting) go back and start the week again. If you are interested to see a Dory boat, Look up "Dory Boats" "Pacific City Dorymen" I was one of five women to do this, we were somewhat the start of more women to go fishing. More later. 'shortshot80..(Nany)
Colleenyoung.....Yes, thanks. Might help to know what to expect. Thank you. (shortshot80 Nancy
Hi Linda-
Frankly I'm not sure what I have in mind, other than to raise awareness levels in our community. Too many times do we experience discovery of a newly diagnosed lung cancer victim who is stage 4 with no hope other than chemo. Too many times we hear of a newly diagnosed stage 4 lung cancer victim, who had been seeing her local doctor who was treating her for pneumonias, or undetermined pulmonary conditions.
Our community is an active retirement community with approximately 2500 folks, two golf courses, a beautiful lake, hiking trails, etc. Truely, the closest thing to paradise that we have found. Yet, tragedy strikes way too often with folks in their sixties and seventies all of a sudden scucomming to lung cancer!
Maybe we need to broaden the discussion to pulmonary disorders including lung cancer...don't know.
Maybe we need to enlist my wife's local oncologist or possibly a Mayo representative...don't know.
Suggestions?
My husband and I commend you both! You have obviously done your home work. We would be willing to fly (in our DL passes) to speak to your community.
My passion is to raise awareness about lung cancer, lung health and pulmonary research so Lungs & Lives can be saved.
We are hopefully starting a Longatudinal Healthy Lungs rRsearch Study in with Mayo Clinic Dr Bruce Johnson & The Healthy Human Research Lab.
One thing this lung cancer journey has taught me is researchers desperately need research funds. This is why my husband Jerry and I co-founded WortmanLungCancerFoundation.com & Running Lungs Walk/Run events two years ago. We are a non profit and have raised $25,000.00 for Mayo Clinic lung research & researchers.
Your thoughts?
Thank you for caring about others and sharing the needs of your community.
Kindest regards,
Linda