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.
You're so right!!! It's never long enough!! We will be married 61 years in June....and they said it wouldn't last 🙂 I'm Stage 4, and as long as I'm on this side of the grass, I'm finding something to be thankful for every day.....especially my guy!
That is so sweet of you! Thank you!
@mjane120, carcinoid or neuroendocrine tumors of the lung are different from other lung cancer types. You may also wish to follow the discussions in the
- Neuroendocrine Tumors (NETs) Support Group https://connect.mayoclinic.org/group/neuroendocrine-tumors-nets/
Here are a couple of discussions that might interest you:
- Typical carcinoids to be removed from lung https://connect.mayoclinic.org/discussion/typical-carcinoids/
- Newly diagnosed-Primary Malignant Neuroendocrine of Lung https://connect.mayoclinic.org/discussion/newly-diagnosed-primary-malignant-neuroendocrine-of-lung/
@fowlair Mary, I just want to let you know that I'm thinking about you, knowing that tomorrow is your anniversary.
Hi Kira, welcome. You may wish to connect with other members living with SCLC in this discussion:
- Small Cell Lung Cancer: Let's connect https://connect.mayoclinic.org/discussion/small-cell-lung-cancer-1/
I'm glad to hear that the cancer did not spread to the lymph node that was removed. How is the recovery from surgery going? When does she start chemo?
How are YOU doing?
Hi @mjane120, welcome! There are some very knowledgeable people in this group. I am continuing to learn something each and every day. Did you happen to see this other recent discussion related to carcinoid tumors?
https://connect.mayoclinic.org/discussion/concerns-after-lobectomy/?pg=1#comment-849475
The lung module/ tumor is or was a carcinoid. The pathology results are still pending. The middle lung was removed. Has anyone here gone through this!
Greetings MJane , Well, hope you are feeling and doing well. Sorry that you have joined this group unwillingly, but good to have you here. This group of Mentors and people just like you are very knowledgeable and helpful. Hope you will ask any questions you need to or just get to know others on here that can give you guidance or information or whatever you may need. They are a great group and have big Ears and big Shoulders!
Thank you
Hi Theresa, I just hit my 4 week mark after LUL Segmentectomy and a small lingular wedge. Also had both breast implants removed due to encapsulation and calcification. All in the same operation. I too still have the soreness and aches and pains of under the front breast incision(for the lung surgery) and the back and side incisions. My surgeon recommended using those lidocaine patches to help ease those pains. Like Aspercream or Solanpas. She said you could cut them to fit the area but do NOT put them on any incisions. I know Mayo offered a booklet for Pain after surgery and how to deal with it without more medications and it talked about Yoga, Tai chi, meditation, etc. You may be able to go on to their website and find it. The best thing, of course, is to talk with your surgeon about what you are allowed to do at this stage of healing. Good luck to you and I hope you heal well!
Cindy