Gallbladder Cancer Stage 4
Comments
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Hi Maudsiemaudsie said:for Sharon
Hi Sharon, like the others, I am surprised to hear of someone so young with GBC. And I am so sorry! However, as was pointed out, she has her youth in her favor. I want to underscore the suggestion that you act immediately to make sure your daughter is seen at a large, prominent cancer center by docs who are very familiar with gall bladder cancer, who know the latest treatment options, have surgical and medical expertise, and can put their knowledge to bear in your daughter's case. The statistics are not pretty, but they are getting better and better all the time, not everything we read is up-to-date. Please let us know how things are going!
Maudsie
I'll keep you in my prayers, along with the others here who are fighting this awful disease. My daughter is tolerating her treatments well so far and I'm just amazed at her attitude. It's too early to determine if the treatments are helping, but she is definitely fighting. I appreciate all the support and info everyone posts up here.
Sharon0 -
Dear Cherylwestie66 said:Your Mom Diagnosed With Gallbladder Cancer Stage IV
Hi Maria: Greetings from Canada. Do not despair about your mom and do not give up hope. I was diagnosed with Stage IV gallbladder cancer (same as T4) in mid-April 2010. They did the same to me - took out my gallbladder that had a 4 cm tumour protruding from it to the liver, cut out a chunk of liver, as well as some nodules on the upper intestine - all cancerous. The prognosis of course was not good. BUT ... I had an MRI last week and the results came in yesterday. No sign of any malignant tumours from the base of the lungs to the pelvis - only a non-cancerous tumour on the liver called a hemangioma and some cysts. That doesn't mean of course that the cancer has gone and that there aren't any cancerous cells or small cancers that can't be seen around somewhere. I suspect they will want to do some chemo on me, too, but I have to wait for the surgery incision to heal which has taken 3 months. So, don't let the doctors give your mom that kind of prognosis! Tell her to fight it and get as healthy as she can with good food and a positive attitude.
Interestingly, gallbladder cancer rates are highest for women in the High Andes of Ecuador and Peru. I've been to Ecuador several times and loved it very much.
Cheryl
Dear Cheryl,
I read your message and I was overwhelmed with gratitude. Thank you for having taken the time to answer and for sharing your experience - you have made a big difference for me. I am so happy that the results of your MRI have been good. I hope with all my heart that everything goes perfect for you and will pray for that. And that you have many more chances to visit my country. If you do so, I would love if you could met my family, they will love to I am sure.
Your message gave me hope much needed. My mom does not know yet that the tumor was cancerous. They have decided to tell her that the results will be out only after fifteen days. This was unclear to me until today, when I spoke with her and she told me she hopes the tumor will be benign. It broke my heart.
In any case, I will try and apply your advice. She is got to fight and I am sure she will. I trust this battle can be fought and won, as your example shows.
Lots of thanks and all the best for you,
Maria0 -
Dear LilyLily50 said:Your Mom - Helena
Hi Maria,
I'm glad that you are joining our little community. I'm so sorry that you Mom has been diagnosed with this terrible disease. My diagnosis was T4 in December of 2005 and I have been in remission for 3 years. The doctor's all seem to give dire prognosis, The statistics regarding this disease are unreliable at best.
I agree with Cheryl, if your mother has been a healthy person she needs to get even healthier and stay postive. Don't not let anyone take away your HOPE and Faith.
She can fight this disease!
Take Care
Lily
Dear Lily,
Thank you so much for your words. They really have had an effect on me, and I will share them with my mom when she knows about her situation. Indeed, faith and hope cannot be forsaken, and your message and that of Cheryl have rekindled them in me. I hope and pray for your continuous good health and will love to keep in touch.
All the best for you,
Maria0 -
Stage IV Gallbladder Cancer and Your MomHelenab said:Dear Cheryl
Dear Cheryl,
I read your message and I was overwhelmed with gratitude. Thank you for having taken the time to answer and for sharing your experience - you have made a big difference for me. I am so happy that the results of your MRI have been good. I hope with all my heart that everything goes perfect for you and will pray for that. And that you have many more chances to visit my country. If you do so, I would love if you could met my family, they will love to I am sure.
Your message gave me hope much needed. My mom does not know yet that the tumor was cancerous. They have decided to tell her that the results will be out only after fifteen days. This was unclear to me until today, when I spoke with her and she told me she hopes the tumor will be benign. It broke my heart.
In any case, I will try and apply your advice. She is got to fight and I am sure she will. I trust this battle can be fought and won, as your example shows.
Lots of thanks and all the best for you,
Maria
Thank you very much. We will all be thinking of you and your mom, too. They didn't tell me for one month - I guess they want us to heal first, get our bodies healthier, to better absorb the bad news and fight the disease.
I would love to visit Ecuador again and you and your family. What part do you live in? I have spent most of my time there around Quito, in the rainforest to the east of Quito, up in the high Andes, down south to Cuenca (did I get that right?), and then along the coast from Guayaquil (spelling?) northwards. It is the most beautiful, friendly, country I've visited. Do you know you have more birds than any other place in South America (I think it was over 7000 at last count). I've seen there the tiniest hummingbird and the biggest hummingbird. A professor friend here in Anthropology married a lovely man from Quito and she studies women's issues there.
Anyways, fight the good fight for your mom.
Cheryl0 -
Linda's SurgeryLinda1949 said:Linda1949 Surgery
Lily, I am Kathleen, Linda's sister. She had her surgery on Tuesday as planned. Drs. did not find obvious signs of cancer on other organs. They took a wedge of her liver at the gallbladder site, small sample of bile tract and the lymph nodes. The preliminary pathology just came in and shows the liver and bile tract free of cancer, but some cancer showed up in lymph nodes (which were removed). Linda is doing well, and recovery is coming along. Family has been taking turns staying with her all day and night to keep her spirits up and cater to her every need. We missed seeing her dr. when he came in with the news today and won't be able to talk to him until Monday. What do you think? I am very hopeful that she has a chance. Do you happen to know what might be the type of treatment she will look forward too? This site has been a "God send" for her. I appreciate your support to her this last week. You are a true angel! Kathleen~
That is very good news indeed. I, too, had my gallbladder removed with its tumour and a big chunk of adjacent liver plus a few nodules on the upper intestine (see my profile and responses on this discussion board). All malignant. They are waiting to start chemo once the incision site has healed completely (it has been almost 3 months). I had an MRI 2 weeks ago and the results show no malignant tumours anywhere so I think they want to do chemo to "clean up" whatever might be there that is too small to see in an MRI or hidden. Keep us posted on Linda's progress.
Cheryl0 -
Daughter with gallbladder cancersharon65 said:Hi Cheryl,
My daughter has
Hi Cheryl,
My daughter has always been a healthy eater and very aware of nutrition. She doesn't feel much like eating but says she's forcing herself to keep from losing weight. She's very petite anyway. Are there particular types of supplements that are recommended? Thanks for your concern.
Sharon
Hi: I drink lots of healthy smoothies (made with good quality whey protein powder, soy milk, any fresh or frozen fruit I happen to have around), as well as the bottled meal replacement drinks (I drink the low sugar ones) when my appetite is poor - they are all full of nutrients and some even are for putting on weight. As for supplements, I looked at reports online very carefully (I'm a botanist and feel we are not using plants for healing as much as we should; after all, taxol for breast cancer is from the yew tree, periwinkle is used to treat leukemia) and here is what I take (this is not to say that your daughter should take them - always let the doctor know what you are taking): first and foremost, paw paw in pill form (only one disributor, Nature's Sunshine) which I take 1 pill 4 times a day with meals; mangosteen juice, 2 tablespoons twice a day with the paw paw morning and with dinner (a fruit that has the highest levels of anti-oxidants of anything and works synergistically with paw paw) (there is also a pill form); selenium; milk thistle (to help the liver); Omega 3; turmeric 3 times a day BEFORE meals; papapa enzyme 3 times a day BEFORE meals; green tea extract (or 1-3 cups of green tea) 3 times a day before meals. I was also taking extra zinc but don't want it to compete with the paw paw. And of course a good multi-vitamin and probiotic. There are several very good books on supplements for cancer. I only chose the supplements that couldn't hurt me and I have told my oncologist I am taking them. Apparently, the paw paw can even be taken during chemo but that is up to the medical oncologist to approve. Lots of fresh fruit and vegetables are key though.
Keep us posted on your daughter's progress.
Any one else out there into supplements like these?
Cheryl0 -
Linda's Surgerywestie66 said:Linda's Surgery
That is very good news indeed. I, too, had my gallbladder removed with its tumour and a big chunk of adjacent liver plus a few nodules on the upper intestine (see my profile and responses on this discussion board). All malignant. They are waiting to start chemo once the incision site has healed completely (it has been almost 3 months). I had an MRI 2 weeks ago and the results show no malignant tumours anywhere so I think they want to do chemo to "clean up" whatever might be there that is too small to see in an MRI or hidden. Keep us posted on Linda's progress.
Cheryl
Thanks Cheryl for your response! I will let Linda know about your fight too. It is so very comforting to have others to talk to!0 -
Maria's MomHelenab said:Dear Lily
Dear Lily,
Thank you so much for your words. They really have had an effect on me, and I will share them with my mom when she knows about her situation. Indeed, faith and hope cannot be forsaken, and your message and that of Cheryl have rekindled them in me. I hope and pray for your continuous good health and will love to keep in touch.
All the best for you,
Maria
Hello Maria,
It is very important to communicate with others regarding this disease. Ask any questions as everyone here has gone through or is going through the same thing that you and your Mom are experiencing. Let us help you if we can. Again this is a terrible disease but not one that we can't win againist. There are some success stories out there and everyday that passes another person has been told that they are scheduled for surgery or that the chemo and/or radiation has shrunk the turmor(s). Try to stay positive and talk to us.
Take Care
Lily0 -
Sharon's daughtersharon65 said:Hi Lily,
I'm in Indiana, but
Hi Lily,
I'm in Indiana, but my daughter is in Florida. We're trying to work out a way to bring her home to be with us but right now it's not possible. She's a fighter, but she has a number of other health issues. Unfortunately she wasn't in good health before her diagnosis. Still, she's tolerating the chemo pretty well. Tough weekend--we've been talking to her siblings about the diagnosis. Thanks for keeping us in your prayers. You are in mine as well.
Sharon
Hi Sharon,
Since you are in Indiana and she is in Florida does she have someone with her to support her? There are some good facilities in Florida. I know as a mother myself I would want to be near my daughter if she was going through something like this. But sometimes it isn't possible and as long as you know that someone is looking out for her best interests then you have to put your faith in her, that other person and God. If she has lived in Florida for awhile and has had other health issues then she probably has some very good doctor's looking out for her. Chemo is never easy and some days will be better than others. It had to have been hard letting the rest of the family know. You are a strong women and you sound like you have a very loving and close family. I agree with Cheryl on the note about fruits, vegetables, and supplements. Smoothies also become a way of life for most of us.
You, your daughter and family are in my prayers.
Take Care
Lily0 -
Linda's SurgeryLinda1949 said:Linda1949 Surgery
Lily, I am Kathleen, Linda's sister. She had her surgery on Tuesday as planned. Drs. did not find obvious signs of cancer on other organs. They took a wedge of her liver at the gallbladder site, small sample of bile tract and the lymph nodes. The preliminary pathology just came in and shows the liver and bile tract free of cancer, but some cancer showed up in lymph nodes (which were removed). Linda is doing well, and recovery is coming along. Family has been taking turns staying with her all day and night to keep her spirits up and cater to her every need. We missed seeing her dr. when he came in with the news today and won't be able to talk to him until Monday. What do you think? I am very hopeful that she has a chance. Do you happen to know what might be the type of treatment she will look forward too? This site has been a "God send" for her. I appreciate your support to her this last week. You are a true angel! Kathleen~
Linda & Kathleen,
What wonderful news! Sorry that I missed your post. I will try to do better. But I see my good friend Cheryl stepped in. Linda is very lucky to have such a strong family support group to help her along with her recovery and next treatment steps. She has taken a positive step towards dealing with this disease. Generally speaking chemo and or radiation will be the next steps. Since there were some cancer cells in the lymph nodes that were removed based on my own experience I had to do some more chemo after my surgery. That way any stray cells can be cleaned up. Tell Linda that I'm praying for her and hope she has a speedy recovery from the surgery.
Take Care
Lily0 -
Linda's SurgeryLily50 said:Linda's Surgery
Linda & Kathleen,
What wonderful news! Sorry that I missed your post. I will try to do better. But I see my good friend Cheryl stepped in. Linda is very lucky to have such a strong family support group to help her along with her recovery and next treatment steps. She has taken a positive step towards dealing with this disease. Generally speaking chemo and or radiation will be the next steps. Since there were some cancer cells in the lymph nodes that were removed based on my own experience I had to do some more chemo after my surgery. That way any stray cells can be cleaned up. Tell Linda that I'm praying for her and hope she has a speedy recovery from the surgery.
Take Care
Lily
Thank you Lily!
Linda is coming home from the hospital this afternoon. I had to fly back to Texas already, but Linda knows I will be back in a flash when she needs me too. The Dr. wants her to come home with the PICC line they had to put in because her veins kept collapsing. She is concerned because of the care that needs to be given to it and she doesn't have an oncology appt for another 10 to 12 days. She meets with the Radiologist next Tuesday. Her spirits are high and now that we both purchased iPhones, we are texting back and forth, playing scrabble and just having a good time despite this disease. I appreciate both you and Cheryl's support. This board's existance certainly needs to be advertised by the surgeons and oncologists. Hope is what we all want, and I know Linda and I have found it here. Thanks for all you are doing to help others. Kathleen~0 -
Linda's SurgeryLinda1949 said:Linda's Surgery
Thank you Lily!
Linda is coming home from the hospital this afternoon. I had to fly back to Texas already, but Linda knows I will be back in a flash when she needs me too. The Dr. wants her to come home with the PICC line they had to put in because her veins kept collapsing. She is concerned because of the care that needs to be given to it and she doesn't have an oncology appt for another 10 to 12 days. She meets with the Radiologist next Tuesday. Her spirits are high and now that we both purchased iPhones, we are texting back and forth, playing scrabble and just having a good time despite this disease. I appreciate both you and Cheryl's support. This board's existance certainly needs to be advertised by the surgeons and oncologists. Hope is what we all want, and I know Linda and I have found it here. Thanks for all you are doing to help others. Kathleen~
Hi Linda & Kathleen,
Yeah you are going home! Standard 6 to 7 days for surgery and recovery. Means no issues from the surgery. What a great sister Kathleen is, back in a flash that is true love. Lot's of people have PICC lines that they take care of themselves or they have a nurse come to their homes. Is that an option for you? The consultation with the Radiologist will give you the answers to the questions that you have. Make a list of the questions as you think of them in the next week that way you won't be tongue tied when you go there. That also goes for the Oncologist too. iPhones are a good way to keep in constant touch with each other. I don't think that many surgeons and oncologists have the time or put forth the effort to see anything outside of their own little world. I'm so glad that we have given you some Hope when everything that you read is bleak at best. Take Care of yourself and keep talking to all of us. We do care about you.
Lily0 -
Dad Diagnosed with Stage 4 Gallbladder Cancerwestie66 said:Stage IV Gallbladder Cancer and Your Mom
Thank you very much. We will all be thinking of you and your mom, too. They didn't tell me for one month - I guess they want us to heal first, get our bodies healthier, to better absorb the bad news and fight the disease.
I would love to visit Ecuador again and you and your family. What part do you live in? I have spent most of my time there around Quito, in the rainforest to the east of Quito, up in the high Andes, down south to Cuenca (did I get that right?), and then along the coast from Guayaquil (spelling?) northwards. It is the most beautiful, friendly, country I've visited. Do you know you have more birds than any other place in South America (I think it was over 7000 at last count). I've seen there the tiniest hummingbird and the biggest hummingbird. A professor friend here in Anthropology married a lovely man from Quito and she studies women's issues there.
Anyways, fight the good fight for your mom.
Cheryl
Hi Everyone,
My dad was diagnosed with stage 4 gallbladder cancer in March 2010 after having his gallbladder removed. CT Scans and a biopsy confirmed that the cancer metastasized to his liver. Since he had several tumors in different regions of his liver, surgery would not be an option (at least not yet). After he healed from his surgery, his oncologist (at the university of chicago) put him on Gemcitabine and Cysplatin. After 6 cycles of chemo, the follow-up CT scan showed minor tumor shrinkage! We were so happy and grateful for the positive news. The plan is to continue the chemo and do another check after 6 cycles. We are praying that the tumors will continue to shrink to the point where he may be a candidate for surgery someday. I have read and been told that this cancer is tough to treat and after time some patients will stop responding to treatments all together.
Does anyone have any success stories on other treatments for metastatic liver tumors? I am specifically interested in hearing about:
-radiofrequency ablation
-chemoembolization
-selective internal radiation therapy (SIRT)
I have asked my Dad's oncologist about each of these, but he didn't seem to be a fan of them and didn't think my dad would benefit from them. We'd be willing to take my dad to a different Dr if these treatments do in fact work.
Thanks to the GBC survivors who have posted on this forum. Your stories and courage are truly inspiring and SO very helpful for those of us caring for someone with GBC. I lost my mother to non-hodgkins lymphoma so I am putting up a fight to keep my dad around as long as possible.
Thanks
Teresa0 -
Linda's SurgeryLily50 said:Linda's Surgery
Hi Linda & Kathleen,
Yeah you are going home! Standard 6 to 7 days for surgery and recovery. Means no issues from the surgery. What a great sister Kathleen is, back in a flash that is true love. Lot's of people have PICC lines that they take care of themselves or they have a nurse come to their homes. Is that an option for you? The consultation with the Radiologist will give you the answers to the questions that you have. Make a list of the questions as you think of them in the next week that way you won't be tongue tied when you go there. That also goes for the Oncologist too. iPhones are a good way to keep in constant touch with each other. I don't think that many surgeons and oncologists have the time or put forth the effort to see anything outside of their own little world. I'm so glad that we have given you some Hope when everything that you read is bleak at best. Take Care of yourself and keep talking to all of us. We do care about you.
Lily
Hello Lily and Cheryl,
This is Kathleen again. Linda is having issues with diarrhea, and just doesn't feel well. She has told her doctor and the oncologist, but they say to just take immodium. She isn't feeling well, and is concerned about starting radiation with having this problem. Getting her body back to accepting solid food again has been a challenge. Do you or anyone else know of any "techniques" that might help her through this? This all started when the hospital gave her a salad immediately after she had been on iv's and a liquid diet for almost two weeks. She was wondering if anyone else had these issues after the liver resection surgery. On the good side, her blood work came back with very good numbers. Thanks again, for the support my sister has been getting here. Kathleen~0 -
Linda's SurgeryLinda1949 said:Linda's Surgery
Hello Lily and Cheryl,
This is Kathleen again. Linda is having issues with diarrhea, and just doesn't feel well. She has told her doctor and the oncologist, but they say to just take immodium. She isn't feeling well, and is concerned about starting radiation with having this problem. Getting her body back to accepting solid food again has been a challenge. Do you or anyone else know of any "techniques" that might help her through this? This all started when the hospital gave her a salad immediately after she had been on iv's and a liquid diet for almost two weeks. She was wondering if anyone else had these issues after the liver resection surgery. On the good side, her blood work came back with very good numbers. Thanks again, for the support my sister has been getting here. Kathleen~
Hi: I certainly did but I was in intensive care at the time. I threw up 2 big bowls of whatever (sorry guys!) after being taken off IV's. They brought me cereal - I tried just a bit and wham, ugliness time! It was mostly bile because they had accidentally cut into my bile duct when removing the gallbladder and resectioning the liver. After that they wrapped me in a big warm blanket and I slept for 6 hours and woke up ravenous. I ate a whole plate of plain boiled white rice with some cooked carrots mixed in. Didn't stay in my body long though - very bad runs (including when the surgeon and his team dropped by to see my progress!). They gave me some pills to encourage the bile to leave my system fast. I don't think the salad was a particularly good idea! Not too much in the way of bulk and you never know with lettuce what might be on it. I had no appetite for quite a while (they say that is because of the compromised liver), like many weeks, but forced myself to eat - boiled rice, high fibre meal replacement drinks, nutritious smoothies. There are some things I still can't eat/drink like coffee. The runs didn't last very long (then you get the other problem of constipation!).
Yeah re the blood work! And what a good idea re the IPhone - I don't even have a cell phone!
I start chemo on August 10 - can't say I'm looking forward to it but something that I must do of course. I'm not getting radiation as there is nothing to radiate.
Keep us posted Kathleen.
Cheryl0 -
After Linda's SurgeryLinda1949 said:Linda's Surgery
Hello Lily and Cheryl,
This is Kathleen again. Linda is having issues with diarrhea, and just doesn't feel well. She has told her doctor and the oncologist, but they say to just take immodium. She isn't feeling well, and is concerned about starting radiation with having this problem. Getting her body back to accepting solid food again has been a challenge. Do you or anyone else know of any "techniques" that might help her through this? This all started when the hospital gave her a salad immediately after she had been on iv's and a liquid diet for almost two weeks. She was wondering if anyone else had these issues after the liver resection surgery. On the good side, her blood work came back with very good numbers. Thanks again, for the support my sister has been getting here. Kathleen~
Hi Linda and Kathleen:
Kathleen you are such a good sister, helping Linda in any way that you can. I think that diarrhea is one of the major side effects of this type of surgery. I lived on Immodium for quite awhile. As far as food goes again I agree with Cheryl, rice, smoothies and meal replacements are the way to go. The ability for her body to digest food is now totally different. You have to learn to be more digilent regarding what you put into your mouth. I love salads but I was told not to eat them while I was having treatments and my surgery. I basically didn't eat salads for two years. Like Cheryl stated you don't really know what is living on that lettuce. Also I was told not to have any fresh flowers in my house once again because of what was living on them that I couldn't see but would end up being toxic to my body.
Glad to hear that her numbers were good. That is very positive. Linda needs to give herself some time to heal from such a radical surgery and just take it one day at a time. It does get better but it won't be soon enough for her. You have to be patient. This disease isn't something that can be fixed right away. It takes time.
Let us know how it is going. Linda took a huge step in making the decision to go thru the surgery and now it is on to the next phase.
Take Care
Lily0 -
Teresa's Dadteresa_g said:Dad Diagnosed with Stage 4 Gallbladder Cancer
Hi Everyone,
My dad was diagnosed with stage 4 gallbladder cancer in March 2010 after having his gallbladder removed. CT Scans and a biopsy confirmed that the cancer metastasized to his liver. Since he had several tumors in different regions of his liver, surgery would not be an option (at least not yet). After he healed from his surgery, his oncologist (at the university of chicago) put him on Gemcitabine and Cysplatin. After 6 cycles of chemo, the follow-up CT scan showed minor tumor shrinkage! We were so happy and grateful for the positive news. The plan is to continue the chemo and do another check after 6 cycles. We are praying that the tumors will continue to shrink to the point where he may be a candidate for surgery someday. I have read and been told that this cancer is tough to treat and after time some patients will stop responding to treatments all together.
Does anyone have any success stories on other treatments for metastatic liver tumors? I am specifically interested in hearing about:
-radiofrequency ablation
-chemoembolization
-selective internal radiation therapy (SIRT)
I have asked my Dad's oncologist about each of these, but he didn't seem to be a fan of them and didn't think my dad would benefit from them. We'd be willing to take my dad to a different Dr if these treatments do in fact work.
Thanks to the GBC survivors who have posted on this forum. Your stories and courage are truly inspiring and SO very helpful for those of us caring for someone with GBC. I lost my mother to non-hodgkins lymphoma so I am putting up a fight to keep my dad around as long as possible.
Thanks
Teresa
Hi Teresa,
Welcome to our little forum. Your Dad's story sounds so familiar to all of us here. Dignosed with gallbladder cancer after removal of his gallbladder. Mets to the liver therefore no surgery yet. Sounds like he is doing well with his treatment and it is working on shrinking his tumor. Gemzar and Cysplatin cocktail seems to be the chemo cocktail of choice lately. It is the cocktail that I had and I am a survivor. This is a very difficult cancer to treat because the statistics are old and outdated. It is becoming more and more recognized almost up there with pancreatic cancer. Once my treatment plan was completed and my oncologist stated we needed to have surgery to get the turmors out then additional chemo after surgery I was ready for it. It took 10 months from diagnosis to surgery when I was originally told twice that there was nothing the surgeon could do for me. I wasn't willing to accept that and I did my best to do everything in my power to get rid of the cancer that was invading my body.
Have you checked the Liver Cancer forum board for your questions. There is alot of information there regarding alternative treatments.
How old is your Dad? He is a lucky man to have a daughter that loves and cares about him enough to want him to be with her always.
Take Care and let us know how he is progressing.
Lily0 -
Gallbladder CancerLily50 said:After Linda's Surgery
Hi Linda and Kathleen:
Kathleen you are such a good sister, helping Linda in any way that you can. I think that diarrhea is one of the major side effects of this type of surgery. I lived on Immodium for quite awhile. As far as food goes again I agree with Cheryl, rice, smoothies and meal replacements are the way to go. The ability for her body to digest food is now totally different. You have to learn to be more digilent regarding what you put into your mouth. I love salads but I was told not to eat them while I was having treatments and my surgery. I basically didn't eat salads for two years. Like Cheryl stated you don't really know what is living on that lettuce. Also I was told not to have any fresh flowers in my house once again because of what was living on them that I couldn't see but would end up being toxic to my body.
Glad to hear that her numbers were good. That is very positive. Linda needs to give herself some time to heal from such a radical surgery and just take it one day at a time. It does get better but it won't be soon enough for her. You have to be patient. This disease isn't something that can be fixed right away. It takes time.
Let us know how it is going. Linda took a huge step in making the decision to go thru the surgery and now it is on to the next phase.
Take Care
Lily
Dearest Lily,
Thanks or all your help. I'm finally up to responding myself. I know that my sister Kathleen has shared with you my health status. The diarhea is better now. Still have to be very careful what I eat. You sure can't count on the hopital. They said to just go home and eat a normal diet. Wrong! I have met with the radiologist and it seems that treatments are recommended along with chemo. I will meet with the oncologist again next week to discuss. I also have a 2nd opinion with another oncologist at the same HMO that has actually treated GBC as the other ocologist I saw has never treated it. They claim that it doesn't make a difference if the Dr. has treated it before or not as they just prescribe according to established protocol. They are all very gloom and doom so thank God for you and others on this blog with encouraging news. I am so fortunate to have great family support. I was never alone in the hospital. My sister Kathleen even leaned over the top of my bed during an earthquake to shelter me! My incision is healing great and I'm ready to move on to the next step (radiation and chemo) and get over it. I'm doing what I can to eat well and walk to make myself as healthy as I can before starting additional treatment. You are the only bright light in all this mess so thank you so much for being there for us.
Linda19490 -
Gallbladder Cancerwestie66 said:Linda's Surgery
Hi: I certainly did but I was in intensive care at the time. I threw up 2 big bowls of whatever (sorry guys!) after being taken off IV's. They brought me cereal - I tried just a bit and wham, ugliness time! It was mostly bile because they had accidentally cut into my bile duct when removing the gallbladder and resectioning the liver. After that they wrapped me in a big warm blanket and I slept for 6 hours and woke up ravenous. I ate a whole plate of plain boiled white rice with some cooked carrots mixed in. Didn't stay in my body long though - very bad runs (including when the surgeon and his team dropped by to see my progress!). They gave me some pills to encourage the bile to leave my system fast. I don't think the salad was a particularly good idea! Not too much in the way of bulk and you never know with lettuce what might be on it. I had no appetite for quite a while (they say that is because of the compromised liver), like many weeks, but forced myself to eat - boiled rice, high fibre meal replacement drinks, nutritious smoothies. There are some things I still can't eat/drink like coffee. The runs didn't last very long (then you get the other problem of constipation!).
Yeah re the blood work! And what a good idea re the IPhone - I don't even have a cell phone!
I start chemo on August 10 - can't say I'm looking forward to it but something that I must do of course. I'm not getting radiation as there is nothing to radiate.
Keep us posted Kathleen.
Cheryl
Dear Cheryl,
Thanks so much for your help. You have corresponded with my sister Kathleen on several occasions. I am finally up to blogging myself. I finally feel human again. My surgery was on 7/6/10. I met with the radiologist this week and they want to radiate along with chemo. I don't have a set date yet but think that I will probably start around the same time that you will start chemo. I have met with an oncologist but he was gloom and doom and hasn't treated it GBC before. I have a 2nd opinion scheduled for next week and at least he has treated GBC. I'll have to pick one of them as my oncologist. They seem to think that it doesn't matter who you pick because they go along with established protocol. Does your oncologist have experience with this cancer? I'm anxious to see what drugs you get. I'll let you know when I find out what I will be getting. I'm not sure if it is different drugs if I'm getting radiation or not. Not looking forward to it but want it to just be over with! Thanks for your help and encouragement.
Linda19490 -
Gallbladder Cancer NewLinda1949 said:Gallbladder Cancer
Dearest Lily,
Thanks or all your help. I'm finally up to responding myself. I know that my sister Kathleen has shared with you my health status. The diarhea is better now. Still have to be very careful what I eat. You sure can't count on the hopital. They said to just go home and eat a normal diet. Wrong! I have met with the radiologist and it seems that treatments are recommended along with chemo. I will meet with the oncologist again next week to discuss. I also have a 2nd opinion with another oncologist at the same HMO that has actually treated GBC as the other ocologist I saw has never treated it. They claim that it doesn't make a difference if the Dr. has treated it before or not as they just prescribe according to established protocol. They are all very gloom and doom so thank God for you and others on this blog with encouraging news. I am so fortunate to have great family support. I was never alone in the hospital. My sister Kathleen even leaned over the top of my bed during an earthquake to shelter me! My incision is healing great and I'm ready to move on to the next step (radiation and chemo) and get over it. I'm doing what I can to eat well and walk to make myself as healthy as I can before starting additional treatment. You are the only bright light in all this mess so thank you so much for being there for us.
Linda1949
Hi Linda: We can correspond during chemo and compare! I will be on gemcitibine and cisplantin, like Lily was. Her treatment was more aggressive than I'll be getting - mine is 6 cycles, a total of 12 treatments. Day 1 will be the two drugs together over about 5-8 hours, Day 2 will be 7 days later and only the gemcitibine over 1 hour. Then 3 weeks "vacation". Then Cycle 2 same as 1. So about 8 months. This is the standard treatment for Gallbladder Cancer in Canada as far as I know. There was a clinical trial done in Toronto this year that compared treatments using cisplantin with either gemcitibine or with capecitabine and the gemcitibine combo worked better so they discontinued the trial. The gem/cis combo was also recommended by the Harvard Univesity cancer centre. I am curious, though, why you are getting radiation if there was no indication of any tumours left (if the cancerous lymph ones were removed during surgery?). Lily, any comments on this? I was told by my oncologist that radiation would serve no purpose if there is no tumour(s) large enough to radiate.
Re the doom and gloom oncologist who hasn't worked on this type of cancer and the one who has - well, I guess I would want some experience there, someone who was positive, and someone who I could relate to and above all liked. You don't need doom and gloom!
Wow! an earthquake while you were in the hospital bed. Brave sister!
I'm so glad you made it through surgery so well.
Cheryl0
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