Another Hurdle
Comments
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Thanks!mamacita5 said:Wishing VERY hard for you
Wishing VERY hard for you Craig. Let us know how it goes for you.
Thanks so much for the support! Looks like I'll be facing more hurdles. The mass in my left lung is fairly small and until they do a biopsy we won't know if it's something new or something that has spread from the right lung. I've about decided to pass on another surgery even if that's what is recommended. Why do I have these thoughts that it's all about the money with these doctors? I also feel that a lot of this stuff is really just a shot in the dark, guess work, following procedures that have "worked the best in the past". I'll definitely do the radiation - it's the one that is more targeted. Don't know about more chemo.......darn, just had my port removed 2 weeks ago! I just don't know.....a lot of thinking to do. I did mention to my Onco about looking at the new blood serum method - need to read up on that - where they remove blood, treat the white blood cells, and re-intro into you body. I need to renew my resolve to beat this though getting a little beaten down..LOL.0 -
CraigCSquaredaway said:Thanks!
Thanks so much for the support! Looks like I'll be facing more hurdles. The mass in my left lung is fairly small and until they do a biopsy we won't know if it's something new or something that has spread from the right lung. I've about decided to pass on another surgery even if that's what is recommended. Why do I have these thoughts that it's all about the money with these doctors? I also feel that a lot of this stuff is really just a shot in the dark, guess work, following procedures that have "worked the best in the past". I'll definitely do the radiation - it's the one that is more targeted. Don't know about more chemo.......darn, just had my port removed 2 weeks ago! I just don't know.....a lot of thinking to do. I did mention to my Onco about looking at the new blood serum method - need to read up on that - where they remove blood, treat the white blood cells, and re-intro into you body. I need to renew my resolve to beat this though getting a little beaten down..LOL.
I am so sorry to hear your news. Do you think it's time for a second opinion? You are sounding a bit as if you don't totally have faith in the doctor(s) you have now. You might feel better if you have consulted someone else. The decisions of course are yours and it will be hard. Try to listen to your body and to your gut. Please keep us informed so we can support you in whatever road you take. Diane0 -
Second Opinionlekkerone said:Craig
I am so sorry to hear your news. Do you think it's time for a second opinion? You are sounding a bit as if you don't totally have faith in the doctor(s) you have now. You might feel better if you have consulted someone else. The decisions of course are yours and it will be hard. Try to listen to your body and to your gut. Please keep us informed so we can support you in whatever road you take. Diane
Diane,
I've thought about getting some other opinions. Just not sure how to go about that. May should call my insurance company as I had worked with someone for awhile that came to my home, etc. I guess she was suppose to be an advocate as well as being a sounding board. It almost seems like the IRS, though...LOL...."we're with the Government and we're here to help you". I also dread starting over with new tests, new forms to fill out, etc....although I'm sure a lot of the info can be shared/forwarded. I need to spend more time on this site and look at all the resources that are available. Thanks for the advice....I need be more proactive.0 -
CraigCSquaredaway said:Second Opinion
Diane,
I've thought about getting some other opinions. Just not sure how to go about that. May should call my insurance company as I had worked with someone for awhile that came to my home, etc. I guess she was suppose to be an advocate as well as being a sounding board. It almost seems like the IRS, though...LOL...."we're with the Government and we're here to help you". I also dread starting over with new tests, new forms to fill out, etc....although I'm sure a lot of the info can be shared/forwarded. I need to spend more time on this site and look at all the resources that are available. Thanks for the advice....I need be more proactive.
I am Canadian so don't know anything about insurance but please ask some questions. The site (American, I think)called "inspire" is very good although if you read too much, as I did, it can get depressing. But the forum is big and you would get lots of help.0 -
Stay strong
Craig, So sorry to hear that you are going thru this again! It can and is so frustrating. Just take it one step and one day at a time. You can do this as others have before you. I am with Diane and thinking a second opinion might give you some peace. Most of the test results etc can be faxed to the facility or surgeon. Getting a second opinion does not commit you, it just gives you another point of view and can be helpful in the decision making process about tx. As far as paperwork.....it's everywhere. I am amazed at how much paperwork with computers these days. I thought they were supposed to eliminate the need for all the forms that constantly repeat themselves. (can you say writers cramp) If you could be more specific on the type and stage of your LC, someone might be able to post who has undergone tx for the same thing. Just a thought. Whatever you decide to do Craig, we are here and you are not alone in this fight. My prayers are with you. Stay strong and keep us posted.
Cheryl0 -
Cherylgrannylove said:Stay strong
Craig, So sorry to hear that you are going thru this again! It can and is so frustrating. Just take it one step and one day at a time. You can do this as others have before you. I am with Diane and thinking a second opinion might give you some peace. Most of the test results etc can be faxed to the facility or surgeon. Getting a second opinion does not commit you, it just gives you another point of view and can be helpful in the decision making process about tx. As far as paperwork.....it's everywhere. I am amazed at how much paperwork with computers these days. I thought they were supposed to eliminate the need for all the forms that constantly repeat themselves. (can you say writers cramp) If you could be more specific on the type and stage of your LC, someone might be able to post who has undergone tx for the same thing. Just a thought. Whatever you decide to do Craig, we are here and you are not alone in this fight. My prayers are with you. Stay strong and keep us posted.
Cheryl
Thanks so much for the input. I've been on a yo-yo the last few days. Contemplating ones own mortality is something I'm sure we've all done. One minute resolving to beat this and the next thinking to just put it in God's hands. My original diagnosis was NSCLC state 3B. I had a small - very slow growing, fairly small mass - in my RL. Went thru the chemo/rad. to reduce the mass to nearly nothing and then the lobectomy last Dec. for the top 1/3 of the lung. Did more chemo after surgery and stopped that a couple months ago. The recent PET shows a new mass in the L.lung. Could be new or a spreading of the prior. If it's spread I'm looking at stage IV. I'm looking at more chemo and radiation and not sure on more surgery.
I do want to get a second opinion....like you said, another point of view. My Onco is so matter of fact, clinical, covering his tail (I elected not to do the last few days of chemo). I've always been a fighter and after licking my wounds for a few days, I'm sure I'll get back to that mind set. It's the waiting that's the hardest.0 -
Hi CraigCSquaredaway said:Cheryl
Thanks so much for the input. I've been on a yo-yo the last few days. Contemplating ones own mortality is something I'm sure we've all done. One minute resolving to beat this and the next thinking to just put it in God's hands. My original diagnosis was NSCLC state 3B. I had a small - very slow growing, fairly small mass - in my RL. Went thru the chemo/rad. to reduce the mass to nearly nothing and then the lobectomy last Dec. for the top 1/3 of the lung. Did more chemo after surgery and stopped that a couple months ago. The recent PET shows a new mass in the L.lung. Could be new or a spreading of the prior. If it's spread I'm looking at stage IV. I'm looking at more chemo and radiation and not sure on more surgery.
I do want to get a second opinion....like you said, another point of view. My Onco is so matter of fact, clinical, covering his tail (I elected not to do the last few days of chemo). I've always been a fighter and after licking my wounds for a few days, I'm sure I'll get back to that mind set. It's the waiting that's the hardest.
Wishing you well my friend as you move forward aging with this nasty stuff.
Hondo0 -
Hi Craig,Hondo said:Hi Craig
Wishing you well my friend as you move forward aging with this nasty stuff.
Hondo
I just read this whole thread and want to interject. Don't give in. Look for a new team of drs. Sounds like you're not sure about the current ones. Don't be afraid to travel if you must to get to the right facility. There are so many options other than surgery. I was stage 4 with met to my spine. (upper right lobe). Surgery wasn't an option. Cyberknife killed it and I'm in remission. That's over 2 years ago. I go for a 3 month scan next week. So far, so good. There is a newer radiation method called Proton Therapy. Even more advanced than Cyberknife. I'm assured that if I need more treatment someday, there will be more options to fight with. I went through all the chemo and radiation too. I even still have the port. Look up Proton Therapy just for kicks on Bing or Google. These types of things should give you hope and please never ever never give up. There are great hospitals and treatment centers all over the place. Keep fighting. Alan0 -
AlanAlanRinHBG said:Hi Craig,
I just read this whole thread and want to interject. Don't give in. Look for a new team of drs. Sounds like you're not sure about the current ones. Don't be afraid to travel if you must to get to the right facility. There are so many options other than surgery. I was stage 4 with met to my spine. (upper right lobe). Surgery wasn't an option. Cyberknife killed it and I'm in remission. That's over 2 years ago. I go for a 3 month scan next week. So far, so good. There is a newer radiation method called Proton Therapy. Even more advanced than Cyberknife. I'm assured that if I need more treatment someday, there will be more options to fight with. I went through all the chemo and radiation too. I even still have the port. Look up Proton Therapy just for kicks on Bing or Google. These types of things should give you hope and please never ever never give up. There are great hospitals and treatment centers all over the place. Keep fighting. Alan
That is good news Alan that you are doing so well and great encouragement for Craig and many others. Go for it Craig!!!0
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