New Member-March diagnosis-August surgery
Comments
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Hello Linda., so glad you
Hello Linda., so glad you have joined us. Congradulations to Bob for doing as well as he has. It's so good to hear success stories. I had surgery in May 2008. I also have done well. I still have problems of when to stop eating. I never feel hunger and I have a problem of not feeling full until I've eaten too much. The consequences of this isn't very comfortable. Even without hunger, I enjoy eating very much.I still need to learn control. Please keep us posted on Bobs progress.
God bless you both,
Sandra0 -
sounds familiar..........
I too had Ivor Lewis at Mayo, MN. My surgeon was Dr Deschamps. My diagnosis was Feb 2010 and surgery in March 2010. Followed by chemo. I too am still getting used to my "new" stomach. I have always been a big eater so tend to want to eat too much. Usually followed by discomfort. I lost 62# post surgery, had it to lose. My six month scan was clean.
I will put you on my prayer list. Best of luck and God Bless.
GerryS age 58, married 36 yrs, 6 grandkids0 -
Mayo treatment and surgeryGerryS said:sounds familiar..........
I too had Ivor Lewis at Mayo, MN. My surgeon was Dr Deschamps. My diagnosis was Feb 2010 and surgery in March 2010. Followed by chemo. I too am still getting used to my "new" stomach. I have always been a big eater so tend to want to eat too much. Usually followed by discomfort. I lost 62# post surgery, had it to lose. My six month scan was clean.
I will put you on my prayer list. Best of luck and God Bless.
GerryS age 58, married 36 yrs, 6 grandkids
GerryS, Thank you for the encouraging words and prayers. It seems my husband doesn't really feel hungry either, and just can't tell when to quit eating. He lost 40 lbs during chemoradiation, and another 10 after surgery. Our oncologist is Omaha had mentioned Dr Deschamps, but when we got there we got an appointment time given to us to meet with Dr Wigle. I believe they must all be very, very good surgeons. He is probably at a more ideal weight now. His nickname used to be "Big Bob", affectionately, of course! I am also expecting we will be offered post surgery chemo. Would you mind telling me what chemo regimen was used in your case and how it went? A clean scan for you-how awesome! We also have grandchildren. 3 as of today, and a new baby girl due in October. We are getting very excited for her arrival. Linda0 -
post surgery chemoBobs1wife said:Mayo treatment and surgery
GerryS, Thank you for the encouraging words and prayers. It seems my husband doesn't really feel hungry either, and just can't tell when to quit eating. He lost 40 lbs during chemoradiation, and another 10 after surgery. Our oncologist is Omaha had mentioned Dr Deschamps, but when we got there we got an appointment time given to us to meet with Dr Wigle. I believe they must all be very, very good surgeons. He is probably at a more ideal weight now. His nickname used to be "Big Bob", affectionately, of course! I am also expecting we will be offered post surgery chemo. Would you mind telling me what chemo regimen was used in your case and how it went? A clean scan for you-how awesome! We also have grandchildren. 3 as of today, and a new baby girl due in October. We are getting very excited for her arrival. Linda
I had 3 scheduled chemo treatments. Cisplatin and 5FU. Cisplatin on first day then a pump attached for 5 days with 5FU. I ended up having only 2 rounds as kidney function was declining and was very dehydrated. Chemo was tough on me. Was glad when it was over.
Were you at St Mary's. Did you meet Dr Price and Bill? They have an excellent staff and we were very happy with our care. I spent 8 days post surgery but about 3-4 months recovery at home. Our daughter was treated at Mayo in 1985 and we were very satisfied then. We are lucky to be only 2 hours from Rochester, NE IA, so we are fortunate. Hope all goes well with "Big Bob", tell him he has friend pulling for him that went thru the same.
Gerry0 -
surgery in mayo also
I too had my surgery in the mayo clinic in rochester mn. I was diagnosed August"09, i had surgery in december of '09. I had THE surgery and did have one big complication but the drs were all super and the nusing staff was the best. I would highly recomend this place to everyone. I believe they saved my life. I had an artory wrapped around my new stomach which was very uncommon. this happened day 4 after my THE surgery. I had a second surgery and they fixed the problem. I went back to work march 1st, 8 weeks after getting home from the hospital. i am a preschool teacher. I have never needed dialation and can eat whatever i like, just in small amounts. I have my next cat scan monday , so the start of scanxiety is on.0 -
Omaha connection
Just scanning through the most recent posts and saw a few EC patients from Omaha. My Dad was diagonosed age 77 T3NOMO back in Nov 08. Had chemo/rad at Creighton and saw Dr. Thome as his Oncologist. Had Ivor Lewis at Creighton in May 09 by Dr. Jason Foster. So happy with his care! Latest scans last month show all clear. He is happy, great attitude, eats all he wants, maintains his weight at 176 and walks my black lab, Gus on a daily basis, rain or shine! The irony of it all is that he has survived (and thrived) with all of his treatment, only to have Parkinsons diagnosed with both he and my Mom...YIKES! Oh well, they live close by and are doing pretty darn well. They see all of their aging siblings dealing with their own trials and tribulations of aging and realize that they don't have it too bad!
All my best to all of you EC warriors and their caregivers!
Katrina0 -
Thanks for sharingGerryS said:post surgery chemo
I had 3 scheduled chemo treatments. Cisplatin and 5FU. Cisplatin on first day then a pump attached for 5 days with 5FU. I ended up having only 2 rounds as kidney function was declining and was very dehydrated. Chemo was tough on me. Was glad when it was over.
Were you at St Mary's. Did you meet Dr Price and Bill? They have an excellent staff and we were very happy with our care. I spent 8 days post surgery but about 3-4 months recovery at home. Our daughter was treated at Mayo in 1985 and we were very satisfied then. We are lucky to be only 2 hours from Rochester, NE IA, so we are fortunate. Hope all goes well with "Big Bob", tell him he has friend pulling for him that went thru the same.
Gerry
Dad was admitted to the Hospital yesterday he was in acute kidney failure from the same chemo treatment. They are planning his surgery for 6-8 weeks after chemo and radiation. It has been very hard on him! He will have his 2nd round of chemo in two weeks!0 -
Dad's in hospitalAmanda_5 said:Thanks for sharing
Dad was admitted to the Hospital yesterday he was in acute kidney failure from the same chemo treatment. They are planning his surgery for 6-8 weeks after chemo and radiation. It has been very hard on him! He will have his 2nd round of chemo in two weeks!
I'm so sorry your dad is in the hospital and for his serious side effect. I know we had some really tough times during chemo and we'll pray that your dad will get great care and start to get better soon. One step at a time and hopefully he will get back on track for his surgery. My husband had to have a lot of hydration, and even extra hydration on the days he wasn't planning on spending a day in the chemo lab. But it helped a lot. I know it is very hard on the kidneys. He actually had fluids before treatment, after treatment, and on some days in between. It is hard on him, and on you. What great support and love you show for him!0 -
Mayo surgerycindyhils said:surgery in mayo also
I too had my surgery in the mayo clinic in rochester mn. I was diagnosed August"09, i had surgery in december of '09. I had THE surgery and did have one big complication but the drs were all super and the nusing staff was the best. I would highly recomend this place to everyone. I believe they saved my life. I had an artory wrapped around my new stomach which was very uncommon. this happened day 4 after my THE surgery. I had a second surgery and they fixed the problem. I went back to work march 1st, 8 weeks after getting home from the hospital. i am a preschool teacher. I have never needed dialation and can eat whatever i like, just in small amounts. I have my next cat scan monday , so the start of scanxiety is on.
It's wonderful to hear from you and about your surgery. I can not even imagine having the first surgery and 4 days later you are back in for another one. Your recovery sounds amazing. And a preschool teacher - what energy you needed to return! Preschoolers never seem to tire out. And you were back so soon! We were concerned about eating also. Did your doctor at Mayo not let you have anything to eat or drink for 4 LONG WEEKS? It was all my husband wanted to do for the last two weeks before he was allowed to eat He was making a list of the top 5 things he was dreaming about having first. Then, a few days before the big day to start eating he got anxiety about eating again!!! Go figure! It went well and he sounds a lot like you. Eating anything he wants, in smaller than usual quantities, except he doesn't feel hungry and can't tell when he is full. I'll be thinking of you having your scan on Monday and pray for a great result! Linda0 -
Omaha Connection, tookatrina846 said:Omaha connection
Just scanning through the most recent posts and saw a few EC patients from Omaha. My Dad was diagonosed age 77 T3NOMO back in Nov 08. Had chemo/rad at Creighton and saw Dr. Thome as his Oncologist. Had Ivor Lewis at Creighton in May 09 by Dr. Jason Foster. So happy with his care! Latest scans last month show all clear. He is happy, great attitude, eats all he wants, maintains his weight at 176 and walks my black lab, Gus on a daily basis, rain or shine! The irony of it all is that he has survived (and thrived) with all of his treatment, only to have Parkinsons diagnosed with both he and my Mom...YIKES! Oh well, they live close by and are doing pretty darn well. They see all of their aging siblings dealing with their own trials and tribulations of aging and realize that they don't have it too bad!
All my best to all of you EC warriors and their caregivers!
Katrina
Your dad sounds amazing! I'm sure it has given you such joy to see him thriving after such a serious diagnosis and surgery. And clear scans-what a blessing. My very good friend just finished 37 years in nursing, all at Creighton, so I have heard they have some very good doctors. It is such a good thing to really like your doctors and feel they are treating you well and individually as a person. Hopefully the Parkinsons will also be kept at bay for a long time by your father's strong will and also your mother's. I'm sure they love having you close by and seeing your dad walk Gus every day must bring a smile to you! Thanks for the good wishes. Linda0 -
Paragraphs!unknown said:This comment has been removed by the Moderator
William, So sorry. It started out as a short little entry and just kept going. Unintended, and when I saw it posted I was a bit overwhelmed myself! I think when I finally did post my fingers couldn't begin to type fast enough!
Here's the soccer paragraph! Love the game. Our son played from age 6, grade school, high school, and college. My husband coached for many of the younger years. Our son is still playing at age 31. He had the honor to play in the Panther's stadium, NC for a Division 1 national championship in college. Creighton University vs UCONN. Unfortunately Creighton lost, but what an experience. Enjoy your game, we miss it, and somehow at our son's age we aren't invited to watch much anymore!
Here's the serious paragraph! You have been there-done that, and know right where many of us are coming from even if we don't know ourselves. Shock-disbelief, and then you lead us right into reality and what you can do to help us learn, be informed, and take charge to find out answers as to what we can, or should be doing. If you don't know an answer you seem to research and find one. Anything to help those with EC, or their caregivers, and families. To see Loretta and your smiling faces here after so many years also encourages me so much. Thank you for all you do and for all those you care about. Linda0 -
Mayo DoctorsGerryS said:post surgery chemo
I had 3 scheduled chemo treatments. Cisplatin and 5FU. Cisplatin on first day then a pump attached for 5 days with 5FU. I ended up having only 2 rounds as kidney function was declining and was very dehydrated. Chemo was tough on me. Was glad when it was over.
Were you at St Mary's. Did you meet Dr Price and Bill? They have an excellent staff and we were very happy with our care. I spent 8 days post surgery but about 3-4 months recovery at home. Our daughter was treated at Mayo in 1985 and we were very satisfied then. We are lucky to be only 2 hours from Rochester, NE IA, so we are fortunate. Hope all goes well with "Big Bob", tell him he has friend pulling for him that went thru the same.
Gerry
Chemo was really tough, and we were glad when it was over, too. Although I think we may get another round post surgery. We will find out soon.
We were at St Mary's. We did not meet Dr Price and Bill. Dr Wigle has another doctor working with him who's name is Cory. We were always trying to call hime Dr _______. And I can't remember his last name, as he said to just call him Cory! Very nice, Cory was, and checked on us a lot. Maybe he was particularly liked because he was the one to take out the nasty chest drain tubes. And the PA was Lisa. Very nice and competent team with Dr Wigle also.
Since you are so close did you do the Chemo at Mayo? Rochester is actually a 6 hour drive for us, but we feel it is well worth it, and we feel fortunate to be able to go there on our insurance. Linda0 -
chemo........Bobs1wife said:Omaha Connection, too
Your dad sounds amazing! I'm sure it has given you such joy to see him thriving after such a serious diagnosis and surgery. And clear scans-what a blessing. My very good friend just finished 37 years in nursing, all at Creighton, so I have heard they have some very good doctors. It is such a good thing to really like your doctors and feel they are treating you well and individually as a person. Hopefully the Parkinsons will also be kept at bay for a long time by your father's strong will and also your mother's. I'm sure they love having you close by and seeing your dad walk Gus every day must bring a smile to you! Thanks for the good wishes. Linda
I had my chemo in Waterloo, Ia as was closer. I had trouble with dehydration so was there several times during chemo getting fluids.
Our doctor here communicated with Mayo on several occasions so we were very pleased with that.
Good luck to all and how about the MIDWEST connection!0
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