Any hepatocellular liver cancer survivors out there?
Comments
-
I am still here
One 9 cm removed back in Feb 2010. So far so good, all numbers normal and stable.. Be positive, we all will beat this thing..
Also, I read your other post and realized that your Father's treatment process is almost same as mine, except I had 2 treatments of Y-90, one on its own and the 2nd combined with the portal emb. prior to the surgery. I am also cancer free and I have no chocie but to be positive on this.. As time goes by, I believe if you set your mind to believe, it will come ture..0 -
Im trying so hard but my dadkohsin said:I am still here
One 9 cm removed back in Feb 2010. So far so good, all numbers normal and stable.. Be positive, we all will beat this thing..
Also, I read your other post and realized that your Father's treatment process is almost same as mine, except I had 2 treatments of Y-90, one on its own and the 2nd combined with the portal emb. prior to the surgery. I am also cancer free and I have no chocie but to be positive on this.. As time goes by, I believe if you set your mind to believe, it will come ture..
Im trying so hard but my dad looks so depressed, he has lost almost 30 lbs in the last two months since he was diagnosed, he looks sick and i think its because he is worrying. His appetite has decreased since surgery, he had some complications with fluid build up and had to have a drain placed as well as a stent placed in his bile duct. He was sischarged home with the drain and I dont think that is good for his spirits, When were you diagnosed? It is priamry HCC? I just havent heard one good thing about this cancer besides "Its very agressive" im so sick of hearing that! Has your cancer spread anywhere? What were your followup plans after surgery?0 -
Time will tellSarahD said:Im trying so hard but my dad
Im trying so hard but my dad looks so depressed, he has lost almost 30 lbs in the last two months since he was diagnosed, he looks sick and i think its because he is worrying. His appetite has decreased since surgery, he had some complications with fluid build up and had to have a drain placed as well as a stent placed in his bile duct. He was sischarged home with the drain and I dont think that is good for his spirits, When were you diagnosed? It is priamry HCC? I just havent heard one good thing about this cancer besides "Its very agressive" im so sick of hearing that! Has your cancer spread anywhere? What were your followup plans after surgery?
Mine WAS primary and was found i Oct 2009, no spread and that's great news. The surgery was done Feb 2010. Forget about the statistic, everyone is different, I don't think there are enough sample size to reflect the accurate stats anyway. Your dad's condition must be good enough for the surgery or the docs will reject that idea. The pain and suffering come with the territory. I was thinking I can be back on my feet in 2 months which I did but it took a lot of pain medication. I am still on the pain killer but down to 2 per day. I have ups and downs, and was told this will take at least 6 months to be back to normal and the scar tissue will still bother me. My onco says no chemo needed at this point, just blood and CT every 3 months for the first 2 years. I lost 25 lbs and I am watching my diet. LIVE EVERYDAY TO THE FULLEST!! Don't worry, he will come around. If he needs some support or someone to talk to, let me know if I can help0 -
stay positive
I had primary HCC and a resection on 12/07 to remove a 7.6cm tumor, had CT done on 2/10 and it look great, then just found out on last CT that cancer came back on resection site with 4.6cm mass. Now doctors want to remove right lube completely. I am scare it may come even after 2nd surgery. This is a terrible illness and very aggressive. Stay positive and trust in God. I will decide between surgery and TACE within the next few days.0 -
Thanks for the replies itjim2204 said:stay positive
I had primary HCC and a resection on 12/07 to remove a 7.6cm tumor, had CT done on 2/10 and it look great, then just found out on last CT that cancer came back on resection site with 4.6cm mass. Now doctors want to remove right lube completely. I am scare it may come even after 2nd surgery. This is a terrible illness and very aggressive. Stay positive and trust in God. I will decide between surgery and TACE within the next few days.
Thanks for the replies it really helps no know we are not alone in this
Jim thats pretty amazing you went three years being cancer free! How much was resected the first time, have they said if your liver has grown since the resection? My dad had a complete right lobe resection already I hope his liver grow back fast! I dont understand why this happens to people like him and you, it is a very scary thing, life changes so fast! Good luck on your decision, at least the mass is small. How often do you go for ct? are they full body ones or just if the liver? 0 -
Sorry Sarah, it was typo, ISarahD said:Thanks for the replies it
Thanks for the replies it really helps no know we are not alone in this Jim thats pretty amazing you went three years being cancer free! How much was resected the first time, have they said if your liver has grown since the resection? My dad had a complete right lobe resection already I hope his liver grow back fast! I dont understand why this happens to people like him and you, it is a very scary thing, life changes so fast! Good luck on your decision, at least the mass is small. How often do you go for ct? are they full body ones or just if the liver?
Sorry Sarah, it was typo, I had resection surgery on 12/09, not 12/07 and the tumor was 7.6cm. My CT on 2/10 was all clear and then a 4.6cm tumor showed up on the resection site on 5/10. my doctor says that the liver will grow back with a few weeks. I don't know whether mine grew back. I have to do CT every 3 months but as you can see, within 3 months, my tumor grew to 4.6cm already but i don't think insurance will pay for more frequent CT.0 -
hcc moved to vertabraSarahD said:Im trying so hard but my dad
Im trying so hard but my dad looks so depressed, he has lost almost 30 lbs in the last two months since he was diagnosed, he looks sick and i think its because he is worrying. His appetite has decreased since surgery, he had some complications with fluid build up and had to have a drain placed as well as a stent placed in his bile duct. He was sischarged home with the drain and I dont think that is good for his spirits, When were you diagnosed? It is priamry HCC? I just havent heard one good thing about this cancer besides "Its very agressive" im so sick of hearing that! Has your cancer spread anywhere? What were your followup plans after surgery?
I had liver resection last may and the tumor spread to back i april thru portal vein. i got back pain, thought i pulled a muscle and went to chiropractor....what a fool.. i will tell you to put it in a nutshell if you ever experience anything unusual...run to you specialist and seek proper treatment ..i had a full blown back spine surgery to repair.i am just finishing rad and have 1st chemo appt next week...will fill you all in.nick........push you dad a long and pray hard0 -
Diagnosed March 2010 stage 4jim2204 said:Sorry Sarah, it was typo, I
Sorry Sarah, it was typo, I had resection surgery on 12/09, not 12/07 and the tumor was 7.6cm. My CT on 2/10 was all clear and then a 4.6cm tumor showed up on the resection site on 5/10. my doctor says that the liver will grow back with a few weeks. I don't know whether mine grew back. I have to do CT every 3 months but as you can see, within 3 months, my tumor grew to 4.6cm already but i don't think insurance will pay for more frequent CT.
Diagnosed March 2010 stage 4 HCC. I had a resection of a 13.5cm tumor on the left side without good margins. I switched hospitals as there were more on the right side that couldnt be resected (about 7-8 largest being 5.125cm). Tried a TACEdeb procedure but had to stop due to a complication, went at it again 3 weeks later and was a success. Just got back from 2 week follow up and scans still no tumors in my liver. I have some in other places but none in my liver anymore and hopefully they dont come back!! Will be treating the lung and adrenal gland ones differently in the next couple months after my liver heals from this procedure. I know its only been 4 months but i'm staying positive, active and still working full time. I've only burnt 2 weeks of vaca for everything I've had done all with pretty speedy recovery thankfully. I've found the fastest way to recovery is get off the pain pills as soon and fast as possible and get yourself moving.
God bless anyone that has to deal with this disease!!0 -
Mike thats awesome news!stage4liver said:Diagnosed March 2010 stage 4
Diagnosed March 2010 stage 4 HCC. I had a resection of a 13.5cm tumor on the left side without good margins. I switched hospitals as there were more on the right side that couldnt be resected (about 7-8 largest being 5.125cm). Tried a TACEdeb procedure but had to stop due to a complication, went at it again 3 weeks later and was a success. Just got back from 2 week follow up and scans still no tumors in my liver. I have some in other places but none in my liver anymore and hopefully they dont come back!! Will be treating the lung and adrenal gland ones differently in the next couple months after my liver heals from this procedure. I know its only been 4 months but i'm staying positive, active and still working full time. I've only burnt 2 weeks of vaca for everything I've had done all with pretty speedy recovery thankfully. I've found the fastest way to recovery is get off the pain pills as soon and fast as possible and get yourself moving.
God bless anyone that has to deal with this disease!!
Mike thats awesome news! Lets put an end to ths terrible disease..Im trying like hell to keep my dad's spirits up even though I want to cry all the time, I still feel like im in shcok somrimes...0 -
KohsinSarahD said:Mike thats awesome news!
Mike thats awesome news! Lets put an end to ths terrible disease..Im trying like hell to keep my dad's spirits up even though I want to cry all the time, I still feel like im in shcok somrimes...
I was just wondering what your pathology report showed after your resection. My dad had his first onc appointment, so far so good. He is gaining weight and feels great. We will go for our first set of scans end of august, all we can do is pray I guess 0 -
SarahDSarahD said:Kohsin
I was just wondering what your pathology report showed after your resection. My dad had his first onc appointment, so far so good. He is gaining weight and feels great. We will go for our first set of scans end of august, all we can do is pray I guess
My report showed no visible invasions with good margin(4/4.5 CM). My last CT showed postop scars on the liver and the rest looked normal, AFP is down to 1.8 from 10,000 before surgery (it is a positive trend over last 3 months). So far so good.. I am praying for all of us and always remind myself to be positive. Sounds like your father has passed the most difficult phase and its on his way to recover..Great news if so>>0 -
HCC - can you help?kohsin said:I am still here
One 9 cm removed back in Feb 2010. So far so good, all numbers normal and stable.. Be positive, we all will beat this thing..
Also, I read your other post and realized that your Father's treatment process is almost same as mine, except I had 2 treatments of Y-90, one on its own and the 2nd combined with the portal emb. prior to the surgery. I am also cancer free and I have no chocie but to be positive on this.. As time goes by, I believe if you set your mind to believe, it will come ture..
Can you possibly help with the questions below?
I have been diagnosed with advanced HCC and metastatic spread to my lungs, preventing resection and radiation and chemo. However I am on Nexavar and anti-inflamatories; both of which seem to be helping.
My interest is to hear from someone that has or is surviving from their real own experiences (rather than a book perspective or what to do).
Koshin, you seem to have this experience to share, and it would be appreciated.
What kinds of food would you suggest that are supportive for persons with advanced liver cancer?
Regarding diets, is a macrobiotic style advisable, or too limiting?
Can you offer suggestions or information on how you should manage your health? (ie exercise type/duration, sleeping, meditation, etc.)
Can you offer suggestions on how would you manage daily life; as I feel overwhelmed?
Can you offer or make suggestions on how you managed time with your family, young children (I have a 3 & 5 year olds), holidays, etc.?0 -
myfamilymyfamily said:HCC - can you help?
Can you possibly help with the questions below?
I have been diagnosed with advanced HCC and metastatic spread to my lungs, preventing resection and radiation and chemo. However I am on Nexavar and anti-inflamatories; both of which seem to be helping.
My interest is to hear from someone that has or is surviving from their real own experiences (rather than a book perspective or what to do).
Koshin, you seem to have this experience to share, and it would be appreciated.
What kinds of food would you suggest that are supportive for persons with advanced liver cancer?
Regarding diets, is a macrobiotic style advisable, or too limiting?
Can you offer suggestions or information on how you should manage your health? (ie exercise type/duration, sleeping, meditation, etc.)
Can you offer suggestions on how would you manage daily life; as I feel overwhelmed?
Can you offer or make suggestions on how you managed time with your family, young children (I have a 3 & 5 year olds), holidays, etc.?
Stay strong and be positive...
AS for your questions,
What kinds of food would you suggest that are supportive for persons with advanced liver cancer?
My personal experience is to have as much fruitS as as possible, low fat diet, no pork/beef, only chiecken.. All kinds of berries, grapes, and kiwi.. They make me feel energized/soothing.
Regarding diets, is a macrobiotic style advisable, or too limiting?
No clue on this one
Can you offer suggestions or information on how you should manage your health? (ie exercise type/duration, sleeping, meditation, etc
I am running 3 to 5 miles two days out of a week. Upper body strength daily for about 10 minutes. I had surgery so the activity is still limited but I believe you can exercise at your regular level.
Can you offer suggestions on how would you manage daily life; as I feel overwhelmed?
Keep yourself busy>> PLan for the worst and hope for the best. It will take a while to sink in. And only time will tell. There is no magical way on this..
AS for your last question, the kids don't need to know everything yet, but you should reach out to family and friends for support. You will have ups and downs (mostly when you are alone). Don't know if you are working, try not to quit or take a break if you can handle the job. ALSO, GET A SECOND OPINION ON YOUR CONDITION
LET ME KNOW IF YOU WANT TO TALK.0 -
Hi,myfamily said:HCC - can you help?
Can you possibly help with the questions below?
I have been diagnosed with advanced HCC and metastatic spread to my lungs, preventing resection and radiation and chemo. However I am on Nexavar and anti-inflamatories; both of which seem to be helping.
My interest is to hear from someone that has or is surviving from their real own experiences (rather than a book perspective or what to do).
Koshin, you seem to have this experience to share, and it would be appreciated.
What kinds of food would you suggest that are supportive for persons with advanced liver cancer?
Regarding diets, is a macrobiotic style advisable, or too limiting?
Can you offer suggestions or information on how you should manage your health? (ie exercise type/duration, sleeping, meditation, etc.)
Can you offer suggestions on how would you manage daily life; as I feel overwhelmed?
Can you offer or make suggestions on how you managed time with your family, young children (I have a 3 & 5 year olds), holidays, etc.?
I have stage 4 HCC with
Hi,
I have stage 4 HCC with mets to lungs and adrenal gland. First off i would ask if you've had a second opinion, not so much on the disease itself but your treatment options? I've had a surgery and a TACEdb procedure done so far. Conventional Chemo isn't usually offered for liver cancer as it isn't very effective. I don't have cirrhosis or hepa and had good liver function so if you have either of those that might be why they aren't offering more options.
A macrobiotic diet is Inline with what you should be looking at. Removing animal protiens and replacing with more plant proteins. Low sugar, low salt, minimal to no red meats and heavy on fruits and veggies.
I still work full time and travel every other week for my job. It's up to you and your situation on if you feel you can or want to continue to work.
As for the kids your's are real young, mine is 10 and she knows what's going on with me and that I could die from it. We had a few conversations and she asks questions every now an then but other than that it's life as usual for the most part.
Dealing with the dx is different for everyone. When first dx'd the cancer consumed every inch of me mentally and physically. I decided to say f@•* cancer and take my life back as much as possible!! I guess I figured if this disease takes me, it isn't going to take everything from until that final day. I make the most out of everything I can.
I know you said you didn't want the book thing but I started reading "anticancer" written by a Dr. That found his own brain cancer by accident. He goes into diet, lifestyle, breakingthe news, etc. It's a good read.
Almost forgot I was also recommended to take maitake mushroom extract from the nutritionist at MSK where I go for treatment and they are the #2 cancer hospital in the US behind MD.
God Bless you and your family in this fight!!0 -
first set lf scanskohsin said:SarahD
My report showed no visible invasions with good margin(4/4.5 CM). My last CT showed postop scars on the liver and the rest looked normal, AFP is down to 1.8 from 10,000 before surgery (it is a positive trend over last 3 months). So far so good.. I am praying for all of us and always remind myself to be positive. Sounds like your father has passed the most difficult phase and its on his way to recover..Great news if so>>
My dad is going for his first set of scans thursday bone scan, abdominal ct and mri as well as a chest ct and labs, we are very nervous...I guess that feeling will never go away, he isin great spirits, hope we get good news. Stage 4, Koshin, and Jim how are all of you doing?0 -
Dad wil be fine..SarahD said:first set lf scans
My dad is going for his first set of scans thursday bone scan, abdominal ct and mri as well as a chest ct and labs, we are very nervous...I guess that feeling will never go away, he isin great spirits, hope we get good news. Stage 4, Koshin, and Jim how are all of you doing?
I just had my full blood panel and CT back.. Normal and stable.. Tumor mark is at 1.4.. The doc said the trend is awesome, from 10,000 B4 surgery, 500, 128, 75, 8, 1.8 and now the 1.4. I am loving it.. The post op CT showed a shadow 3 months ago is now gone.. I am confident and I am sure your Dad will be fine..0 -
Dad will be fine..SarahD said:first set lf scans
My dad is going for his first set of scans thursday bone scan, abdominal ct and mri as well as a chest ct and labs, we are very nervous...I guess that feeling will never go away, he isin great spirits, hope we get good news. Stage 4, Koshin, and Jim how are all of you doing?
I just had my full blood panel and CT back.. Normal and stable.. Tumor mark is at 1.4.. The doc said the trend is awesome, from 10,000 B4 surgery, 500, 128, 75, 8, 1.8 and now the 1.4. I am loving it.. The post op CT showed a shadow 3 months ago is now gone.. I am confident and I am sure your Dad will be fine..0 -
hcc with new mets to lungstage4liver said:Hi,
I have stage 4 HCC with
Hi,
I have stage 4 HCC with mets to lungs and adrenal gland. First off i would ask if you've had a second opinion, not so much on the disease itself but your treatment options? I've had a surgery and a TACEdb procedure done so far. Conventional Chemo isn't usually offered for liver cancer as it isn't very effective. I don't have cirrhosis or hepa and had good liver function so if you have either of those that might be why they aren't offering more options.
A macrobiotic diet is Inline with what you should be looking at. Removing animal protiens and replacing with more plant proteins. Low sugar, low salt, minimal to no red meats and heavy on fruits and veggies.
I still work full time and travel every other week for my job. It's up to you and your situation on if you feel you can or want to continue to work.
As for the kids your's are real young, mine is 10 and she knows what's going on with me and that I could die from it. We had a few conversations and she asks questions every now an then but other than that it's life as usual for the most part.
Dealing with the dx is different for everyone. When first dx'd the cancer consumed every inch of me mentally and physically. I decided to say f@•* cancer and take my life back as much as possible!! I guess I figured if this disease takes me, it isn't going to take everything from until that final day. I make the most out of everything I can.
I know you said you didn't want the book thing but I started reading "anticancer" written by a Dr. That found his own brain cancer by accident. He goes into diet, lifestyle, breakingthe news, etc. It's a good read.
Almost forgot I was also recommended to take maitake mushroom extract from the nutritionist at MSK where I go for treatment and they are the #2 cancer hospital in the US behind MD.
God Bless you and your family in this fight!!
Hi
My situation is pretty similar to you. I had a tumor growing on my liver when I was pregnant with my son. I had a biopsys when I was 25 wks pregnant and the path report was benign. I had the baby and 8 mos late had surgery to remove the 17cm tumor. Next day in hospital I get the path report that the tumor has transformed to malignant and I am diagnosed w hcc with no history of hepatitis or cirrhosis. I did chemo for 7 mos and just had my first scan since chemo, my oncologist tells me it has mets to lungs and immediately referred to MD Anderson or Mary Crowley Research center here is Dallas.
I trying to decide now what to do, I know MD reputation however, my oncologist referred me so fast, he didn't offer any treatment to me. I was wondering have you done any clinical trial or what type of treatments are you going0 -
koshinkohsin said:Dad will be fine..
I just had my full blood panel and CT back.. Normal and stable.. Tumor mark is at 1.4.. The doc said the trend is awesome, from 10,000 B4 surgery, 500, 128, 75, 8, 1.8 and now the 1.4. I am loving it.. The post op CT showed a shadow 3 months ago is now gone.. I am confident and I am sure your Dad will be fine..
Hi Koshin! Your profile is very similar to mine, and I wonder if you would share the name of your doctor and hospital with me. Mine has prescribed Sorafenib and I have undergone general radiation, but they are reluctant to offer any other treatment due to the size of the tumor. I'm not ready to give up!!0 -
Liver resectionstage4liver said:Diagnosed March 2010 stage 4
Diagnosed March 2010 stage 4 HCC. I had a resection of a 13.5cm tumor on the left side without good margins. I switched hospitals as there were more on the right side that couldnt be resected (about 7-8 largest being 5.125cm). Tried a TACEdeb procedure but had to stop due to a complication, went at it again 3 weeks later and was a success. Just got back from 2 week follow up and scans still no tumors in my liver. I have some in other places but none in my liver anymore and hopefully they dont come back!! Will be treating the lung and adrenal gland ones differently in the next couple months after my liver heals from this procedure. I know its only been 4 months but i'm staying positive, active and still working full time. I've only burnt 2 weeks of vaca for everything I've had done all with pretty speedy recovery thankfully. I've found the fastest way to recovery is get off the pain pills as soon and fast as possible and get yourself moving.
God bless anyone that has to deal with this disease!!
Hi stage4liver. I chose my screen name having read your posts because our profile seems so similar, except that I am likely much older. My tumor is 11 cm now, and the doctors considered it to be unresectable or treatable because of the size. I am very surprised to hear that they operated on yours, and desperately want to consult with another doctor about this. Would you please share the name of your doctor and hospital with me?
I can't give up now! I know this cancer can be beaten, and I need more time with my family!!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