The Cancer Survivors Network (CSN) is a peer support community for cancer patients, survivors, caregivers, families, and friends! CSN is a safe place to connect with others who share your interests and experiences.
CEA
Comments
-
belindahill -
I think the best advice anyone can give you, is to tell you to let
your physicians decide what test results are important, and
which ones are not.
There are many "markers" for cancer and CEA is only one;
one single marker doesn't mean much when a diagnosis is
being considered! Anything can raise or lower "CEA", so
don't panic with the news (and "2" is within the normal range).
Think: good health!
John -
2 is good
2 is a good level.
Mine was 65 in November, after 22 weeks of chemo, now i am 2.5.
i was excited about that number, but my onc said the same thing... this is just ONE marker.
the CT scan is the thing that is my "tell all" for my Cancer and thats scheduled for about a week or two from now.
keep smiling and don't panic too much about any ONE test or marker.
but, remember... 2 is good!
my best -
2 is good
2 is a good level.
Mine was 65 in November, after 22 weeks of chemo, now i am 2.5.
i was excited about that number, but my onc said the same thing... this is just ONE marker.
the CT scan is the thing that is my "tell all" for my Cancer and thats scheduled for about a week or two from now.
keep smiling and don't panic too much about any ONE test or marker.
but, remember... 2 is good!
my best -
I was dx 4 months ago. First
I was dx 4 months ago. First CEA was 44 and it's dropped everytime and is now at 0.9. I've had one scan since the original, and the tumors -- rectal and mets to liver and a couple of nodes, had shrunk about half. Great news but they still say "chemo for life" and use the "t" word (terminal). I have 2 oncologists at 2 different institutions, that are working together, and they both say this is great and will follow the current path (folfiri, vectibix) until it stops working, then try something else, probably folfox. Still considered inoperable. The goal is to keep me alive until something else comes along. But the CEA gives me hope, whether warranted or not. Good luck to you, my friend! Dan -
Hi jay, my husband is on chemo for like, and having chemo till it stops working, then we try something else, all the very best for you. xJayhawkDan said:I was dx 4 months ago. First
I was dx 4 months ago. First CEA was 44 and it's dropped everytime and is now at 0.9. I've had one scan since the original, and the tumors -- rectal and mets to liver and a couple of nodes, had shrunk about half. Great news but they still say "chemo for life" and use the "t" word (terminal). I have 2 oncologists at 2 different institutions, that are working together, and they both say this is great and will follow the current path (folfiri, vectibix) until it stops working, then try something else, probably folfox. Still considered inoperable. The goal is to keep me alive until something else comes along. But the CEA gives me hope, whether warranted or not. Good luck to you, my friend! Dan
Discussion Boards
- All Discussion Boards
- 6 Cancer Survivors Network Information
- 6 Welcome to CSN
- 122.6K Cancer specific
- 2.8K Anal Cancer
- 456 Bladder Cancer
- 312 Bone Cancers
- 1.7K Brain Cancer
- 28.6K Breast Cancer
- 408 Childhood Cancers
- 28K Colorectal Cancer
- 4.6K Esophageal Cancer
- 1.2K Gynecological Cancers (other than ovarian and uterine)
- 13.1K Head and Neck Cancer
- 6.4K Kidney Cancer
- 681 Leukemia
- 803 Liver Cancer
- 4.2K Lung Cancer
- 5.1K Lymphoma (Hodgkin and Non-Hodgkin)
- 242 Multiple Myeloma
- 7.2K Ovarian Cancer
- 70 Pancreatic Cancer
- 493 Peritoneal Cancer
- 5.6K Prostate Cancer
- 1.2K Rare and Other Cancers
- 544 Sarcoma
- 743 Skin Cancer
- 659 Stomach Cancer
- 192 Testicular Cancer
- 1.5K Thyroid Cancer
- 5.9K Uterine/Endometrial Cancer
- 6.4K Lifestyle Discussion Boards


