survivors of Terminal Stage 4 lung cancer
Comments
-
Thank you Joe for sharing andsoccerfreaks said:my version
suebloom:
I was diagnosed with head/neck cancer the first of september, 2005, surgery in october, chemo and rads into january of '06. In June of '07 results of a cat scan showed 'cancer' across both of my lungs, shotgun-spread. No surgery, no rads, only palliative chemo-therapy offered, and the advice that I had 'a minimum of ten months to live.'
In the meantime, I started taking Keflex for an infection in my jaw and lower face area. Subsequent CAT and PET scans (about two months later) showed that the 'cancer' had disappeared, with one exception: it had clearly been a lung infection of some sort, misread by the experts.
Ultimately, the one remaining node was removed and biopsied, and though it proved to be squamous cell cancer (same as my head/neck cancer) they decided to remove that lower right lung lobe since there was no evidence of any cancer around it. (The node was too small to stage or to determine whether it was indeed metastasis from the tongue/neck.)
Last november ('08) I was diagnosed NED and received the same dx just three weeks ago.
I have a page and a blog on this site, if you would care to read more.
Best wishes to you, suebloom!
Take care,
JoeThank you Joe for sharing and giving hope.
0 -
Urgently need a referencedennycee said:Z is correct.
Joe has not been on the boards now for a couple years. He had a parting of the ways with ACS and hasn't been back. I'm a 5 year survivor of stage 4 lung cancer so I know it can happen. Your overall health going in I'd often a good indicator of how you will do. My best to you and hopes for a terrific outcome!
hello dennycee, I am so happy to hear your story. I urgently need a reference for my father. He is similar like your story. He's been diagnosed with non small lung cancer adenocarsinoma and has been in chemotherapy for 2 yrs. I need a reference where do you have your treament? And the doctor as well please? we have tried so many drugs of chemotherapy and immunotherapy as well but some works for 1 month and some dont. Thank you so much.
0 -
Nsclc
I was diagnosed with nsclc in 3/2014 had 1/3of lung removed the cancer came back 1year later in lung,lymph nodes 4 brain mets I had 4 gamma knife 30 rounds radiation on lymph nodes
Began opdivo 14,months ago last 5 scans no new growth or movement.feel opdivo might have giving me some more time
Praying for all of you anyone else having luck with opdivo
0 -
God bless you guys and alwayspattig1968 said:hi...my husband's nasophargeal cancer has spread to his lungs
hi my name is Patti....my husband was first diagnosed with nasophargeal cancer in 2005 and received treatment for about 7 wk of radiation and then returned again in 2007 once again he received radiation with a shot of chemo 1x a week..Here we are in 2009 and he has once again been diagnosed with this dreadful disease....this time it has spread to his lungs..about 2cm....we will be going away for the Easter Holiday....and then he will start chemo again....no radiation.....I also cry each and every day ....but out of his vision...Dont't know how I will control this one when we are away.....He has been depressed ...but not admitting to it.....Today I told him to get out of bed or we will cancel our reservations.....I love him deeply ...and been married for 40 years...and can not stand to lose him...But told him that he also has to fight and not give up....He's a Marine....And as we know they are the "Best"....so I told him once again to get out of bed and let's fight....We were told that this time no cure....hello there never was...but only that they can "control" it.....I truly believe that this time it will do the job....I have so much faith...that God will carry us through this...thanks for letting me vent...feel free to do the sameGod bless you guys and always have Faith becasue it's stronger then people think.
0 -
lung cancer
my husband went from a stage 2 to a stage 4 while taken strong chemo. how is that possible and why could't they have tested him sooner instead of waiting for a month after the chemo ended than only ordered a cat scan which led to another pet scan. Shouldn't he had the pet scan as soon as he got done chemo to check then. also he was in the local hospital with an uper GI bleed they couldn't pinpoint and blamed it on his low plateletts. He was bleeding from the recdom when he went in . I think his cancer doctor should have ordered a pet scan then instead of a cat scan.
0 -
lung cancer
there was no other cancer showing up on the pet scan when he took the chemo now he is full it just didn't work that is what the oncoligest said. Now he is taken Opdivo when won't cure it.
0 -
Hi , how can i get the storyfrajuma5 said:Thank you for sharing this inspiring story about your dad
Hello PeterJr,
I wanted to thank you for sharing your dad's story. It is certainly inspiring, and believe it or not lifted my dad and my family's spirit.
My dad was diagnosed about a week ago with stage IV lung cancer, which we did not expect at all, as my dad has not been displaying any symptoms other than his chronic cough (which he has had for years, way before they found something in his xrays, and scans).
I came across your story after googling stage iv survivors and I am happy to have stumbled on your dad's story. I showed it to my dad, and it gave him even more of a fighting spirit. I guess that's what we all need with all of our cases, examples of hope. You and your father are such an example of hope and optimism, that after reading this, my dad has asked me to print your post and to put it on the refrigerator to look at daily. I see it as a token of survival, so God Bless you!
The doctor said that his cancer at this point is incurable, but I adamantly feel that it should not be hopeless. Since his diagnosis, we also have heard of survival stories, one which came from our home country (Philippines) of a famous newscaster who was diagnosed in 2008 and was given only three months to live. He miraculously lived for almost 5 years past his prognosis when he succumbed to the cancer just this month.
We are faithful that our dad will live through several more years and we are faithful that he manage a normal life even with this cancer. Thank you to stories like yours, there is much hope for those in despair. Just because this cancer and the stage that it is in is incurable, it does not need to be a stamp of a death sentence.
God Bless you, your family and especially your father.
frajuma5Hi , how can i get the story that Peter Jr had posted.
0 -
thank you, i enjoyed yourMadelynJoe said:Your Husband
Dear Patti:
I can well understand your distress. My husband is a six year prostate cancer survivor and I am a 4 year nonsmall cell lung cancer survivor. When your husband's Doctors say they can "control" it - they mean it. I know quite a few people that are very long term cancer survivors through my cancer support group. One lady has been treated for metastatic ovarian cancer for 12 years now and she and her husband live active and full lives! I know breast cancer survivors of 20 to 30 years! Our group has long term survivors from every type of cancer imaginable. Metastatic disease can be controlled, you better believe it!
I have been on both ends of cancer; I've been a caregiver for a loved one and I've been a patient. If I had to pick, I would say it was harder going through my husband's diagnosis that mine (because I love him so much). You sound as if you two are very much in love. If you allow yourself give in to the "doom and gloom" thing; you're going to be miserable and so will he.
You are a Marine's wife - you can do ANYTHING! You are accustomed to sacrifice (when he has been on deployment) and you are TOUGH! This does not mean you cannot feel the pain or cry the tears. I have a friend that set a timer for 5 minutes every time she wanted to cry and sometimes had to set it the second time but, she did not give into the doom thing; she stayed positive. Today she is a 10 year breast cancer, double mastectomy survivor!
Put your arms around your husband and tell him something like ... "Our love is strong and we can do anything. We've gone through bad times before and we will do it again. Let's get out there and fight!"
Arm yourself with information. Learn everything you can about this type of cancer and the latest treatments. Don't be afraid to question your doctors or suggest things. You have to be your own advocate in the medical community today. A good doctor will not mind your questions/suggestions. Go to the MD Anderson and Sloane Kettering web sites and get some good information from the experts.
By the way, in case you do not know, when you are searching for information, nasophargeal cancer will apply, NOT lung cancer - even though the small tumor is in the lung. You will still need to search info regarding nasophargeal cancer - the original site.
Sorry this "Pep Talk to the Troops" went too long but, you two sound like fighters and I think you can win this "War".
Best regards,
Madelynthank you, i enjoyed your reading, it gives a guy some confidence..
0 -
Congratulationssuebloom said:surviving
I am a survivor of stage iv lung cancer......diagnosed 7/08.Congratulations
0 -
Thank you very much,, can iCaringRN said:Lung Cancer RN
I have been working with Lung cancer patients for quite a while now and I am sorry about your confusion. Let's just say you are not alone. They normally do not radiate multiple areas, which it sounds like your husband has. (Unless they become bothersome - painful, etc.) So it sounds like they are treating things the way they should - with multiple chemos. The first treatment didn't work, so they will try another one and should continue to do so. If they decide to stop, seek another opinion. There are trials out there and I can not tell you if there is one out there your husband is appropriate for. Everyone is different so just hang in there! Let me know if you have any other questions! I am here to help! I have a passion for what I do and I want to help people through this difficult time in their lives.........the last thing a patient or family should have to do is wonder if what they are doing is the right thing.Thank you very much,, can i ask you some questions some time,
0 -
stage 4 lung cancer
I would love to hear survivor stories of this cancer,, please
0 -
wow, thank you for your storyPeterJr said:Stage 4 Lung Cancer
My father age 85 was diagnosed with stage 4 lung cancer in July 2009. He was told he had 6 months to live. Well my father has always been one that will decide his destiny. Here is what I and several of my family member did.
1) We put him on a diet of cancer fighting foods
2) We cut his sugar intake as much as possible. He has been a diabetic for 30 years anyway.
3) No carbonized sodas
4) Plenty of water
5) We Prayed
6) Keep stress away and try to keep his spirits high.
7) We Talked about the Cancer
He immediately started Chemo. After all the treatments as cat scan was performed. He was told by the Doctors that his stage 4 Cancer is now Stage 2 Cancer. It was decided to give his radiation. He went through all the treatments except the last two and was told to go home and he would be examined in about a month. Two weeks ago my father went back for his cat scan from head to toe. The Doctors could not find the cancer!
I do not know what the future holds for my Dad and Cancer. All I do know is that he is healthy now!
I hope this helps with Caring for your Grandma!wow, thank you for your story,,
Basil
0 -
Start a New Discussion
Taylors 2018, I would suggest starting a new discussion thread. This one is so old that it was difficult to find your post in it. There are many 10+ years survivors of Stage 4 lung cancer. There re some on this site and quite a lot on Inspire.com.
I was diagnosed just last summer with stage 3a, and CT scans thus far have shown no evidence of disease.
All the best to you.
0 -
same diognosisnessaducky said:More about your treatment Joe, please
Joe,
My mom was just diagnosed with stage 4 non small cell lung cancer which has metastasized to the pleural lining and space outside the pleural lining of her right lung. She is still up and about and wearing her high heels. She is strong and amazing and forever an inspiration to me. I would like to know what your course of treatment has been. We are just now trying to get her in with doctors and finding her treatment as soon and as fast as we can. This is all so sudden, but I know my mom will get through this and overcome it with God. I am just trying to educate myself with disease and am looking for any and all help.
I appreciate any response to this post. God Bless you!!
-VanessaVanessa, this sounds like the same thing that i have, i just had surgery on the 5th of july to have my right lung lobe removed,when i woke up inthe recovery room, they told me they didnt go through with the lobe removel because it has metastasized to the plueral lining, it sure would of been nice to know this before, they started this, i still am sore from this procedure, i go tomorrow to talk to a doctor about what treatment they think is best, i to know that god will get me through this, i am learning as much as possible, and it is hard to know what is the best thing to do, so many ppl say not to do conventional treatment, while others say the oppisite, its so confusing, im praying that god will lead me to the right thing,
0 -
same diognosisandiques said:Stage IV NSCLC already in remission!
We're ALL terminal in the end! Don't let the statistics scare you (even though I did!)... I was dx Stage IV NSCLC adenocarcinoma (inoperable) in Jan 2009. Underwent three rounds of chemo ( Carboplatin/Taxol /Avastin ) and then had a CT scan for assessment last week. I'm in remission already and I have to say that the chemo wasn't bad either -- so MUCH better than in the past. SO ... call it a miracle or call in modern-day progress, but whatever it is, I'm happy as a clam! I attribute it to not only my treatment, but also to BIG support in the form of prayers from lots of folks. STAY POSITIVE by all means because. no matter what, we all need to enjoy whatever days we DO have on this earth. We could be hit by a Mack truck tomorrow! BTW, I also highly recommend The Lung Cancer Alliance for great support and discussion. They are under the umbrella of the "Inspire" network. Check them out! Best of luck!i can only hope that goes as well for me
0 -
same diognosisandiques said:Stage IV NSCLC already in remission!
We're ALL terminal in the end! Don't let the statistics scare you (even though I did!)... I was dx Stage IV NSCLC adenocarcinoma (inoperable) in Jan 2009. Underwent three rounds of chemo ( Carboplatin/Taxol /Avastin ) and then had a CT scan for assessment last week. I'm in remission already and I have to say that the chemo wasn't bad either -- so MUCH better than in the past. SO ... call it a miracle or call in modern-day progress, but whatever it is, I'm happy as a clam! I attribute it to not only my treatment, but also to BIG support in the form of prayers from lots of folks. STAY POSITIVE by all means because. no matter what, we all need to enjoy whatever days we DO have on this earth. We could be hit by a Mack truck tomorrow! BTW, I also highly recommend The Lung Cancer Alliance for great support and discussion. They are under the umbrella of the "Inspire" network. Check them out! Best of luck!i can only hope that goes as well for me
0 -
same diognosisandiques said:Stage IV NSCLC already in remission!
We're ALL terminal in the end! Don't let the statistics scare you (even though I did!)... I was dx Stage IV NSCLC adenocarcinoma (inoperable) in Jan 2009. Underwent three rounds of chemo ( Carboplatin/Taxol /Avastin ) and then had a CT scan for assessment last week. I'm in remission already and I have to say that the chemo wasn't bad either -- so MUCH better than in the past. SO ... call it a miracle or call in modern-day progress, but whatever it is, I'm happy as a clam! I attribute it to not only my treatment, but also to BIG support in the form of prayers from lots of folks. STAY POSITIVE by all means because. no matter what, we all need to enjoy whatever days we DO have on this earth. We could be hit by a Mack truck tomorrow! BTW, I also highly recommend The Lung Cancer Alliance for great support and discussion. They are under the umbrella of the "Inspire" network. Check them out! Best of luck!i can only hope that goes as well for me
0
Discussion Boards
- All Discussion Boards
- 6 CSN Information
- 6 Welcome to CSN
- 121.9K Cancer specific
- 2.8K Anal Cancer
- 446 Bladder Cancer
- 309 Bone Cancers
- 1.6K Brain Cancer
- 28.5K Breast Cancer
- 398 Childhood Cancers
- 27.9K Colorectal Cancer
- 4.6K Esophageal Cancer
- 1.2K Gynecological Cancers (other than ovarian and uterine)
- 13K Head and Neck Cancer
- 6.4K Kidney Cancer
- 671 Leukemia
- 794 Liver Cancer
- 4.1K Lung Cancer
- 5.1K Lymphoma (Hodgkin and Non-Hodgkin)
- 237 Multiple Myeloma
- 7.1K Ovarian Cancer
- 63 Pancreatic Cancer
- 487 Peritoneal Cancer
- 5.5K Prostate Cancer
- 1.2K Rare and Other Cancers
- 540 Sarcoma
- 733 Skin Cancer
- 653 Stomach Cancer
- 191 Testicular Cancer
- 1.5K Thyroid Cancer
- 5.8K Uterine/Endometrial Cancer
- 6.3K Lifestyle Discussion Boards