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Vital Info


Elizabeth (elizabeth1227)


July 7, 2011


aim: Elizabeth1227


Westlake Village, California 91361


December 27, 1952


Cancer Fighter

Cancer Info


Anal Cancer


February 12, 2010


Stage 2


02


Grade 1


Negative


Negative


Yes


Yes


Reconstructive Surgery, Mastectomy, Lymph Node Removal


Radiation Therapy


Fluorouracil (5-FU)


Herceptin


Feeling sick, CT/Pet Scans


That I am not in control of cancer only how I cope with it.


Just by being there and knowing people care


kills cancer but makes you sick


iliac lymph node


Wellness Community


get your rest, don't push yourself


find a cancer support group, PRAY and TRUST GOD, live your life as normally as possible, get out when you can





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Posts: 9
Photos: 0
Events: 0
My Supporters: 39
Comments: 34
Views: 6068
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Elizabeth's Cancer Blog

Really tired, too much chemo for me?

Hi Everyone,

It’s been awhile since I posted. I have had 9 treatments of the 12 recommended of the FOLFOX. Each treatment has taken a toll on me. The first few had me home bound for about 8 days. Now I am home bound for 12 days. I get hooked up every other Monday(last one May 7th), 49 hours each time of chemo is a lot. It is like filling a gas tank and when it is full then I have to go through all the symptoms of it leaving my body. That takes about 4 full days after I get unhooked. And it is rough due to constipation from the anti-nausea stuff they give me in the IV. I tried the 8th treatment without it and threw up every 10 minutes for 4 straight hours. Won’t do that again. The last treatment and the one before I felt and feel like not finishing. I just don’t feel good. This chemo regiment is accumulative and I think MY BODY has had enough. The nurse who hooks me up at home said about 20% of the people only get to the 10th treatment due to the fatigue. My oncologist said he would be happy if I tolerated 6 treatments and any after that was “gravy”. BUT the famous oncologist (Dr. Heinz Joseph Lenz, Director of USC Colorectal Oncology) who he sent me to for an opinion said I needed all 12 treatments. When I told him that my oncologist said I needed only 6 he said “he is trying to give you a gift, you need all 12”.
I also think about the long term affects of all this chemo. As all of you had 192 hours when we first went through the initial treatment with the radiation, now I can add 441 hours more. That is a total of 633 hours of chemo. I am also vitamin D deficient. I am now taking 50,000 units of vitamin D once a week. Just started that last week. Can any one tell me do I need to be taking Calcium with that? The pharmacist said I should be but neither doctor (my oncologist or my GP) mentioned it.
It is all so confusing. If chemo lowers your immune system and having a lower immune system increases your chances of getting cancer what are you suppose to do? And if I don’t do what they are recommending I will regret it later if my cancer comes back. And if I stop now I will feel like I gave up and PERSEVERANCE is my strongest character asset. But it is a little frightening to continue in the way I feel physically and I do lose it for at least one night when I am hooked up. I do get over it and I know I am getting stronger through all of this emotionally. Have you heard “What doesn’t kill you makes you stronger”? So true, so true. And ALL the doctors say “There is no right answer”. GREAT!
I have stayed away from “alternative” ways of dealing with cancer due to what happened to Farrah Fawcett and also I attended a funeral last Monday of a friend who was in GREAT SHAPE. She has ran a marathon the week before they found her Stage IV cancer eighteen months ago. She was healthy and ate right. She did the FOLFOX treatment too. She was able to get out more than I have, but I have had 7 surgeries, chemo now twice, radiation twice. She was 4 years younger than me and I am 59. Re-cap I have had breast cancer twice, anal cancer which spread to a lymph node in my iliac area (hip area). They said the cancerous lymph node was encapsulated. I had it surgically removed 11/2/11. Then started this FOLFOX as insurance for any micro-scopic cells that may be left. Sometimes I feel guilty about complaining when I know people who have to be on chemo for the rest of their lives. What also makes it difficult to continue is there is NO CLINICAL DATA to show there is ANY BENEFIT from doing this chemo. But it seems like the people who have had cancer more than once when they stop treatment it spreads.
I don’t want to stress too much about this. I know the answer will come for what I need to do or not do. All of you are a part of this with me. I know I am not alone and am so grateful for this site so I DON”T FEEL ALONE. THANK YOU. Based on all my body has gone through I am feeling it is time to stop but not sure. Like they said “There is no right answer”. I so appreciate any suggestions from all of you.

I love the song “The Climb”. For those of you who watch American Idol, I think Hollie Cavanaugh did a better job than Miley Cyrus who sings it. We are all climbing our “mountains”, we must keep the faith, it is about “The Climb”. I want to do my best in every area of my life, I am so tired.

Gratefully, Elizabeth

Angelica, Nicole (Lady Of The Larynx) threw a punch at your cancer.
Kellye sent you a prayer.
4 people sent you a hug.

Hi Elizabeth—
Of course only you can make this decision, based upon how you feel, input from your docs, etc. However, I will tell you what I would do if I were in your situation. I would put my head down and push through it. I know it seems like you’re darned if you do and darned if you don’t. I just don’t think I could live with myself if I passed up the last few treatments and the cancer was not gone. I am SO sorry you are having such a rough time tolerating the treatment and have to make this decision. When I was in treatment, I really didn’t think I could do the last 3 radiation treatments. However, a good friend of mine reminded me that there would be no do-overs and it was now or never. I guess my opinion is based on that very wise advice. I would keep fighting.

Whatever your decision is, your friends here at BFAC will stand beside you and support you. I will keep you in my thoughts and prayers.

Hugs—
Martha

And sometimes it isn’t that there are no right answers, there are just no answers. We just do what we feel we have to do, to do all and whatever we can to beat this disease. Take it one chemo treatment at a time—and persevere. But whatever you do, we’ll all understand and stand by you. Big hug for you and sorry for the toll this is taking on you. Hang in there, Elizabeth!

Wow, you have had a battle to fight! Keep fighting! :)

Hi Elizabeth – Like Martha, I wish I knew how I would resolve this if I were you…I think I would rely on the perseverance that you mention and try to push on to the end. Only three more!

As for Vit D and Calcium, yes I would take the calcium, the original radiation takes a toll on your bones and you need to supplement. Vitamin D only comes from supplements or from exposing your skin to the sun – you can do a little of the latter but you don’t want to do too much, so calcium! Google for Dr. Christine Northrup’s article on “A Diet that Protects Against Osteoporosis” for a good discussion on this issue.

Pleaase let us know how you are as you move forward on the course of action you choose!

XOXOXO

Dear Elizabeth, I’m so glad to see your post. I really appreciate how you’re fighting with all you’ve got to even be here trying to decide about doing those 3 more treatments.
Not having had a harsh chemo I can’t fully imagine what you’re going through. ...Small comfort, but I think about how at least you get to own your decision; no one can take that away from you.
And you can rest assured that you get unconditional support here, whatever you do.
You are awesomely fierce, going at this head on. Thank you for taking the time to share all this with us.
Hugs to you Elizabeth, Nicole

Trust yourself! You will make the right decision – whatever you do. You are a fighter

Hi Liz;

Nice to hear from you. Sorry you are feeling so bad.

I, too, have been having more problems, so I am not posting much. They have found Cancer has severely damaged my right heel..there is hardly anything left to walk on..just took the bone away. I am going into surgery on June 8, hopefully, otherwise I will not be able to walk, and their will always be this pain I am going through. I have a walker, (I do not use), a cane ( I have to use, but am getting used to) and crutches, that kind of scare me (fall?)

Me and you are about the same age, I am 57, and we both have had a very rough time! I can not get out to much either. Are you starting to get used to it?
The surgery will put me out of commission while the crutches etc. are on, but I would not walk every again, if I didn’t do this, and I just couldn’t face that.

You are right, I think we are getting stronger, in some ways. Good observation!

Love you

Barb

IT'S BENIGN!!!!

THANK YOU GOD! I am so relieved. I finally got good news with my cancer. I still don’t know what it was, but IT’S NOT CANCER! I am pretty drained from this week. And then Monday morning I will get hooked up again for another 49 hours. Eight treatments to go.
Thank you all for your prayers and good wishes!

God Bless You, Elizabeth

Paul, Texas Jeff like this.

Elizabeth, that’s great news. So happy and relieved for you!

Fantastic, amazing, wonderful news! That should help give your spirits a lift as you continue through treatment. Very happy for you!

Woohoo! Thank you for sharing this EXCELLENT news! What an answer to prayer! Thank You, God!

I am so glad to hear that your faith is growing stronger and that you’ve felt God close to you lately. My faith has grown tremendously during this whole cancer mess, too. I understand that feeling of closeness you described. It even shows up in my blood pressure and heart rate sometimes. Amazing!

I am SO relieved that the new issue is benign!

Love and hugs and continued prayers,

Danean

YESSSS! WONDERFUL! THANK YOU FOR THE NEWS!

So happy for your great news!

so so so happy for you!
xoxo

Good! Good for you – well done body and well done spirit for carrying Elizabeth through another challenge! Wishing you all the best for the remainder of your treatment. Be well. much love, janet

Hi Elizabeth!

This is just the BEST news! I am so very happy for you and can only imagine the relief you are feeling right now. I hope the rest of your treatment goes well and that you have no more scares like this. Thanks for sharing your great news with us—God is good! Keep us posted.

Hugs—
Martha

Yahoo! Excellent news. Here’s to hoping the rest of your treatment goes along smoothly.

Dear Elizabeth,

Wonderful news – now you can just focus on one thing and push through and get better!

Hurrah!
Leanne

I’m very happy this has turned out well; now, in a “Reepacheap” fashion, Keep your nose to the Sky and sail onward! (My litte excerpt from Narnia)

Fantastic news! I am so happy for you.

Dear Elizabeth, My spirit just did a jump for joy when I saw your “IT’S BENIGN!” title.
That sure is worth some lovely deep breaths, to keep carrying you forward.
Your faith is amazing, especially the leap of faith you’ve made to continue being such an awesome cancer warrior.
I wish you the most comfort possible this week.
Thanks for sharing this wonderful news, as we all get to touch a little piece of benign news.
Hugs, Nicole

YAY! It is not cancer! So very happy for you!

Been away so just saw your blog. What wonderful news & a great relief for you. Hugs Annabelle

YAY! So happy for you!






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