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geckosfeet

(9,644 posts)
2. "Available" - yes - you never know what is the right direction to go do you.
Sun May 19, 2013, 07:30 AM
May 2013

I think that there are general guidelines but in the end it's a personal decision about what (and if) treatments to undergo.

I am very curious about wholistic diet and nutrition based approaches.

Thanks for your thoughts auntAgonist.

auntAgonist

(17,257 posts)
3. I sure hope you find what you're looking for.
Sun May 19, 2013, 07:37 AM
May 2013

I'm no help when it comes to that.

Please know I wish you all the best.

A very personal decision for sure. No one should ever fault another for making the best choices for them.

kesha.

Nay

(12,051 posts)
6. I am so sorry. You finished one round of chemo about a year ago, yes?
Mon May 20, 2013, 05:54 PM
May 2013

If you're looking for a respected book on the nutritional aspects of cancer care, please read Anti-cancer by David Serban-Schreiber. It was recommended to me by an onco physician's assistant.

My nephew, a brainy science guy, is battling prostate cancer; he keeps up with all the scientific literature (and lectures on it at medical conventions) recommended that I eat 3 white button mushrooms per day and drink 3 cups of green tea per day, because these two items showed a great deal of activity in inhibiting tumors. I have breast cancer; I'm a year out from surgery and radiation, and was just cleared to start having mammograms just once a year again. I was Stage IC, and so far it looks like I'm doing well, but it can come back on me any time, I know.

I want to give you some

geckosfeet

(9,644 posts)
9. Hi. Thks for your thoughts.
Mon May 20, 2013, 09:18 PM
May 2013

Yes i finshed a round of surgery/radiation/chemo about a year ago.

So i like mushrooms and green tea. Will check that author. I just started Keith Block's book , "Life Over Cancer".

 

olddots

(10,237 posts)
7. have you found a group yet ?
Mon May 20, 2013, 07:45 PM
May 2013

I don't live there anymore but there has to be a group near you and I bet there are good ones.

geckosfeet

(9,644 posts)
8. Not yet. Still caught up in doctors aptps etc. Getting ready for chemo.
Mon May 20, 2013, 09:13 PM
May 2013

Have to make arrangements at work. Talking to family. But you are right. I took a quick look. There seems to be some nearby.

Tab

(11,093 posts)
10. Sucks
Tue May 21, 2013, 05:04 PM
May 2013

Sounds like it's on the move.

I live north of Boston myself. Feel free to PM me.

Don't know what support groups are down there, but start with something like Dana Farber Cancer Center. There have to be a zillion groups in and around Boston (not knowing exactly where you are). If you're something like Springfield, I couldn't say, but again, must be a bunch. Something like Lowell, even more (on the outskirts like Burlington). Let me know where you are and I'll see what I can dig up.

BTW, what's the original diagnosis?

Hoping the best for you.

geckosfeet

(9,644 posts)
11. Hi. Yes it does suck. I live in the
Tue May 21, 2013, 05:48 PM
May 2013

Milford area. Regional hospital here has Dana Farber cancer center. I am going to check them out.

Original diagnosus was stage 1 esaphageal cancer but they found some in lymph nodes in the pathology exam. That was end of 2011. Had surgery in Oct. 2011. Radiation then chemo.

Yea. Its back and on the move. Really want to explore integrated treatment and looking for facilities.

2theleft

(1,137 posts)
12. My dad had lung cancer, a kind they had only seen in less than .3% of patients
Sun Jul 7, 2013, 10:36 PM
Jul 2013

His whole treatments were basically reserach, because it was so rare that they had no protocol to go buy. He served 3 tours in Vietnam, and towards the end, the scientists finally determined that the cancer was probably caused by agent orange exposure. This tiny man - maybe 5'6" if he stood up straight, maybe weighed 140 lbs battled for TEN YEARS just to have more time with my mother and me (he was really my step-dad, but more of a father to me than the "real" one). We lost him 2 years ago February.

I think what I want to say, with the uniqueness of his disease, and the right doctor team, and his willingness to try anything to hang around a bit longer, he was able to fight and do pretty good for 10 years and he was stage 4. He had 2 periods of remission thrown in, but then it would come back about a year later. I truly do believe that a lot of it is in the fight and just how much a person can handle. My Ellis was tiny, but he was strong. And he made our family a family. He showed me how I want to act if I'm ever sick - you just keep going on, you keep doign the important things (family/friends/fun), and you keep fighting and asking questions and trying whatever they want you to try if you think you can do it. 10 years was a long time to have with someone who was only expected to live about 2 after first diagnosis.

You, geckosfeet, you fight the good fight, however you can fight it. You let us know how we can help you fight it, and let your family know how they can help you fight it. It's definitely a team sport, at least that is how it felt for our family. Ellis was the quarterback, the doctors were the coaches and we were his defensive line.

I am sending healing, good, strong thoughts your way.

geckosfeet

(9,644 posts)
13. Thank you 2. Thanks for your thoughts, the wonderful remembrance and the encouragement.
Mon Jul 8, 2013, 01:09 AM
Jul 2013

one edit: I think that I will come back to read your post often...

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