Anyone a long term survior - what stage were you.
I am a survior baby (just 6 month since surgery).
callie
Comments
-
I love the term "survivor baby"
Callie
I love the term survivor baby! thank you for the optimism! We all need it here since we have lost some dear folks to this disease. I also think that the "fear" of return makes many of us (family as well) reluctant to even "call" themselves a survivor!!! I want to share your post with my dad... It really is the attitude, baby steps, faith (face it--God's will & love), great Dr's, caregivers & support that help us all through this EC maze!
But I notice---compared to other cancers---EC folks are justifiably more cautious calling themselves "survivors" before year 5. That is a shame == so thanks for starting the ball rolling to give others the option to look at themselves with maybe a little more HOPE. I have found through difficult circumstances that it is difficult to see the glass half full (like when my dad was so sick with follow up chemo---loosing weight, etc---but HEY he was (& is) alive!!!! He unfortunately lost his little brother to this same disease 5/10, so now we are more aware of how well he is doing---considering the "alternatives". It is in the perspectives...
He is also back at being a volunteer fireman (light duty though)! His surgery was 12/09---so... WOW he is a 9 month SURVIVOR BABY!!!! I can't call him a survivor yet---but I love your new term!!!!
thanks Callie!
Kim0 -
I'm brand new tonight & don't know how to navigate or post thingunknown said:This comment has been removed by the Moderator
I just joined and can't figure out how to post questions or comments - all I can do is hit
reply to someone else's post??? I'm a 66 year old grandma of 10 who had chemo/radiation and then the Ivor Lewis surgery. That was mid=May & I've been hospitalized for the last two months from many complications. I sailed through chemo/radiation without one side effect but this surgery has nearly killed me. I've lost 20 pounds and started as a size 2. I went to Mayo Clinic in MN (only a 2-hr drive for me) and the surgery was done by the head of thoracic surgery - he does 40 of these every year and the hospital unit handles 200 a year. The main problem was that they discharged me after only seven days. I was home one day and then hospitalized locally for 3 weeks for double pneumonia. One thing after another- I've only been home for 2 weeks since.
Please assist me in knowing how to navigate, leave comments, etc. I don't even know for sure how to get back to this site!
Nancy Edwards age 66
ECIII (T2 N1 M0)
Ivor Lewis @ Mayo Clinic May 17, 20100 -
look under cns helpcrystalbay said:I'm brand new tonight & don't know how to navigate or post thing
I just joined and can't figure out how to post questions or comments - all I can do is hit
reply to someone else's post??? I'm a 66 year old grandma of 10 who had chemo/radiation and then the Ivor Lewis surgery. That was mid=May & I've been hospitalized for the last two months from many complications. I sailed through chemo/radiation without one side effect but this surgery has nearly killed me. I've lost 20 pounds and started as a size 2. I went to Mayo Clinic in MN (only a 2-hr drive for me) and the surgery was done by the head of thoracic surgery - he does 40 of these every year and the hospital unit handles 200 a year. The main problem was that they discharged me after only seven days. I was home one day and then hospitalized locally for 3 weeks for double pneumonia. One thing after another- I've only been home for 2 weeks since.
Please assist me in knowing how to navigate, leave comments, etc. I don't even know for sure how to get back to this site!
Nancy Edwards age 66
ECIII (T2 N1 M0)
Ivor Lewis @ Mayo Clinic May 17, 2010
I am new too, so can't help much
LOOK at the top of the screen on click on CNShelp.0 -
HURRAYK_ann1015 said:I love the term "survivor baby"
Callie
I love the term survivor baby! thank you for the optimism! We all need it here since we have lost some dear folks to this disease. I also think that the "fear" of return makes many of us (family as well) reluctant to even "call" themselves a survivor!!! I want to share your post with my dad... It really is the attitude, baby steps, faith (face it--God's will & love), great Dr's, caregivers & support that help us all through this EC maze!
But I notice---compared to other cancers---EC folks are justifiably more cautious calling themselves "survivors" before year 5. That is a shame == so thanks for starting the ball rolling to give others the option to look at themselves with maybe a little more HOPE. I have found through difficult circumstances that it is difficult to see the glass half full (like when my dad was so sick with follow up chemo---loosing weight, etc---but HEY he was (& is) alive!!!! He unfortunately lost his little brother to this same disease 5/10, so now we are more aware of how well he is doing---considering the "alternatives". It is in the perspectives...
He is also back at being a volunteer fireman (light duty though)! His surgery was 12/09---so... WOW he is a 9 month SURVIVOR BABY!!!! I can't call him a survivor yet---but I love your new term!!!!
thanks Callie!
Kim
kim
Thanks for the reply, I like your optimism too.
Your comments help me to see things clearer. Now I am proud to say I am a SURVIVOR BABY.
Tell you dad we look forward to His one year Surviror baby birthday party.
Look on my sight, and see the poem i wrote, I think you would enjoy it.
God Bless
ps I am at work, so I can't write much.
With Love
callie
Survivor baby 6mos.0 -
I had surgery in May
I had surgery in May 2008--CT scan in Nov 2008 which showed I was C free. I am a SUVIVOR of stage 111 EC with 2 lymph nodes in stomach. I don't know all the codes so I just write it out. I will be coming up on what I celebrate as my 2nd birthday--Yaaaa! So glad you are doing well ! Keep us posted.0 -
happy birthday Sandysandy1943 said:I had surgery in May
I had surgery in May 2008--CT scan in Nov 2008 which showed I was C free. I am a SUVIVOR of stage 111 EC with 2 lymph nodes in stomach. I don't know all the codes so I just write it out. I will be coming up on what I celebrate as my 2nd birthday--Yaaaa! So glad you are doing well ! Keep us posted.
Sandy
So glad you are doing well. Can't get the smile off my face.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
- 734 Skin Cancer
- 653 Stomach Cancer
- 191 Testicular Cancer
- 1.5K Thyroid Cancer
- 5.8K Uterine/Endometrial Cancer
- 6.3K Lifestyle Discussion Boards