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.

Hi there. I know of Mayo Clinic Connect because I'm on the PMR group. Diagnosed with lung cancer after a CT scan with contrast a week ago so I'm early on. PET scan and biopsy to follow, but that all takes time. Thought I'd get started here. I'll be reading, and I'm sure I'll have more to add in the future. Thanks for all that you do. Kathy

REPLY
@kmeikle1

Hi there. I know of Mayo Clinic Connect because I'm on the PMR group. Diagnosed with lung cancer after a CT scan with contrast a week ago so I'm early on. PET scan and biopsy to follow, but that all takes time. Thought I'd get started here. I'll be reading, and I'm sure I'll have more to add in the future. Thanks for all that you do. Kathy

Jump to this post

Oh gosh, @kmeikle1, I'm just catching up with this post. I'm sorry to hear that you have lung cancer to add to your polymyalgia rheumatica (PMR).

Kathy, have you had the PET scan and biospy in the meantime? How are you doing?

REPLY
@kmeikle1

Hi there. I know of Mayo Clinic Connect because I'm on the PMR group. Diagnosed with lung cancer after a CT scan with contrast a week ago so I'm early on. PET scan and biopsy to follow, but that all takes time. Thought I'd get started here. I'll be reading, and I'm sure I'll have more to add in the future. Thanks for all that you do. Kathy

Jump to this post

Good morning Kathy and welcome to the Lung Cancer group. With PMR you certainly don't need one more thing, do you? I was a heavy smoker and was not surprised at the news. However, no matter if you have suspicions or not I was definitely shocked at hearing those words. How are you dealing with this?

You do have a head start in being familiar with medical care and illness. This will help you with your journey. Two possible next steps will be a PET scan and a biopsy. Biopsies aren't always needed nor advised in some cases and there are varied reasons for this. In the 6 lung cancers that I have had, I've only had 1 biopsy as a tool for diagnosis. And I am very thankful for the caution taken with this.

But PET scans are a wonderful tool for confirming cancer suspicion. Be prepared to spend some time at the hospital when you have a PET. There is a lot of protocol surrounding the injection and wait time (usually an hour or so) paperwork, etc. You might have already had one for other reasons so this might be a moot point.

Do you have dates set for the PET scan as yet?

REPLY
@colleenyoung

Oh gosh, @kmeikle1, I'm just catching up with this post. I'm sorry to hear that you have lung cancer to add to your polymyalgia rheumatica (PMR).

Kathy, have you had the PET scan and biospy in the meantime? How are you doing?

Jump to this post

@colleenyoung Hi Colleen, thanks for checking in. I did have my PET scan and my biopsy is scheduled 9/28. The PET clearly showed the large lung mass and other places lit up as well. I hope to know more the week following my biopsy. Emotionally, I'm doing well. My faith provides a lot of peace. I am dealing with undiagnosed pain around my mid-section that interferes with sleep. Annoying but I guess it goes with the territory. I'll keep in touch. Kathy

REPLY
@merpreb

Good morning Kathy and welcome to the Lung Cancer group. With PMR you certainly don't need one more thing, do you? I was a heavy smoker and was not surprised at the news. However, no matter if you have suspicions or not I was definitely shocked at hearing those words. How are you dealing with this?

You do have a head start in being familiar with medical care and illness. This will help you with your journey. Two possible next steps will be a PET scan and a biopsy. Biopsies aren't always needed nor advised in some cases and there are varied reasons for this. In the 6 lung cancers that I have had, I've only had 1 biopsy as a tool for diagnosis. And I am very thankful for the caution taken with this.

But PET scans are a wonderful tool for confirming cancer suspicion. Be prepared to spend some time at the hospital when you have a PET. There is a lot of protocol surrounding the injection and wait time (usually an hour or so) paperwork, etc. You might have already had one for other reasons so this might be a moot point.

Do you have dates set for the PET scan as yet?

Jump to this post

@merpreb Hi Merry. I suppose I was shocked too. I had a persistent cough for months but assumed that was allergies. I do have a lot of peace, but I'm dealing with some pain issues and that's not fun. I did have a PET scan which showed the large lung mass and other areas of interest 🙂 I'll have a biopsy of my lung 9/28. Six lung cancers? You've earned your place as a mentor! I appreciate you checking in and establishing a dialogue. Thanks, Kathy

REPLY

Hello, my name is Sheri Helseth from Fresno. Just got told after biopsy I have lung cancer and am having an MRI on Friday and next week Pet scan, then Oct 10 the results

REPLY
@grandmasheri

Hello, my name is Sheri Helseth from Fresno. Just got told after biopsy I have lung cancer and am having an MRI on Friday and next week Pet scan, then Oct 10 the results

Jump to this post

Welcome to the lung cancer group, Sheri. Did you have suspicions of lung cancer? It's quite a shock to be told this, even if it's out of the blue. It kind of knocks you off your feet, right? Well, let me help you up. Monday I'll be celebrating 25 years of surviving lung cancer. I'll be glad to help you all I can.

You have now entered the world of cancer tests, lab tests, blood tests, and anything that they can find to test. But it will all help with deciding, with you, what kind of cancer you have and the best way to treat it.

Do you have the results of the biopsy yet? Have your doctors told you anything else or answered your questions?

REPLY

They don’t want to tell me anything until after the next 2 tests are done however all results of test are on the web through a MyChart app. Of course I don’t understand a lot so I have to research the terms. I don’t see that they ran geo testing on the biopsy and that concerns me after reading through answers on this page. That’s one of the questions I’m going to ask on Oct 10th when I go for my results. I know from the results I have adenocarcinoma.

REPLY
@grandmasheri

They don’t want to tell me anything until after the next 2 tests are done however all results of test are on the web through a MyChart app. Of course I don’t understand a lot so I have to research the terms. I don’t see that they ran geo testing on the biopsy and that concerns me after reading through answers on this page. That’s one of the questions I’m going to ask on Oct 10th when I go for my results. I know from the results I have adenocarcinoma.

Jump to this post

Waiting for results and appointments is so difficult. It’s likely that a lot is happening during this time, even though it feels like nothing is happening. The docs are coordinating and lab tests are being completed. The MRI and PET will be help to know if the cancer is contained to the lung. And the biopsy tissue is likely being tested to see exactly what type of cancer it is, and if it is expected to be responsive to certain therapies.
Hopefully they have good options for you at your next appointment! Take care, hang in there, Lisa

REPLY
Please sign in or register to post a reply.