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This Crazy Cancer Journey

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Nancy View Drop Down
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Post Options Post Options   Thanks (0) Thanks(0)   Quote Nancy Quote  Post ReplyReply Direct Link To This Post Posted: Apr 13 2009 at 8:11am
Denise,
 
When Lori had that scare in January, I kept repeating arthritis, arthritis, arthritis, and for you I will repeat what you have written
NO CANCER
NO CANCER
NO CANCER
CLEAN BONES
CLEAN BODY
 
......and I have you wrapped in a blanket of loveBig%20smile
Love and Hugs,
Nancy
 

Nancy
DD Lori dx TNBC June 13,2007
Lumpectomy due to incorrect dx of a cyst
mastectomy July 6 2007
chemo ACT all 3 every 3 weeks 6 tx Aug-Nov
28 rads ended Jan 2008
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gerriesue View Drop Down
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Post Options Post Options   Thanks (0) Thanks(0)   Quote gerriesue Quote  Post ReplyReply Direct Link To This Post Posted: Apr 13 2009 at 12:56pm
Loved reading the peeps posts...made me laugh out loud!!   Thinking of you today Denise and will be saying your NO CANCER mantra at my yoga class, adding my voice to yours and all the others here. And I am very glad to hear we can have some sugar, I have always felt chocolate helped my mood a great deal.
57 yrs. old at DX Oct. 2008 Stage 1, Grade 3, TNB, 1.7 cm tumor,Negative nodes TX partial masectomy, 4 rounds A/C, 4 rounds Abraxane
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trip2 View Drop Down
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Post Options Post Options   Thanks (0) Thanks(0)   Quote trip2 Quote  Post ReplyReply Direct Link To This Post Posted: Apr 13 2009 at 1:25pm

Good luck Denise!Heart

 

Gerrisue my sister gave me a year's subscription to Yoga magazine and I really enjoy.  What I would enjoy more now is if I could get my legs and body into some of those positions.  Mantras I can do, no physical wear and tear on a body that won't bend.LOL

Stage 2 2003
Stage 1 2007
BRCA 1+
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Beth Anne View Drop Down
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Post Options Post Options   Thanks (0) Thanks(0)   Quote Beth Anne Quote  Post ReplyReply Direct Link To This Post Posted: Apr 13 2009 at 1:36pm
Denise sending you no cancer vibes...... good luck honey!!!!

Love,
Beth Anne
Dx 5/07 DCIS Stage3 gr9 A/C x 6, Abrax x 16 Bi-Mass 2/08
Navelbine x 12, finished radiation end of July 08. DX Brain Met's 2/09StageIV
CK3/09.Brain resection4/09 WBR
Dreaming of dancing with Ned!
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krisa View Drop Down
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Post Options Post Options   Thanks (0) Thanks(0)   Quote krisa Quote  Post ReplyReply Direct Link To This Post Posted: Apr 13 2009 at 2:10pm
i subscribe to yoga journal---and wow!  if only i could get my body to contort into some of those poses--i look at these gumby type people and really believe that cancer cells would not dare enter a body that practices the cobra, locust, dancing tree, downward dog, etc. poses.
Smile
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Post Options Post Options   Thanks (0) Thanks(0)   Quote BrendaF Quote  Post ReplyReply Direct Link To This Post Posted: Apr 13 2009 at 3:34pm
Think again.
Dx 2005 2 cm, 5/12 nodes, A/C + T, 28 rads.
Dx mets 12/07 mediastinal and supraclavicular nodes, carbo + taxotere X 6.
brain, lymph, pleura, bone mets. Started Xeloda 8/24/09
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krisa View Drop Down
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Post Options Post Options   Thanks (0) Thanks(0)   Quote krisa Quote  Post ReplyReply Direct Link To This Post Posted: Apr 13 2009 at 4:00pm
no one is immuned.
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Post Options Post Options   Thanks (0) Thanks(0)   Quote gerriesue Quote  Post ReplyReply Direct Link To This Post Posted: Apr 13 2009 at 5:59pm
I go to a Restorative Yoga class. I call it "Laying around with Props". It is very restful, no really strange positions. But, it is really nice and helps me stretch areas that haven't moved much during chemo. I highly recommend the class. The teachers seem very responsive to helping if they know what areas are bothering you or make it unable to do certain things.
57 yrs. old at DX Oct. 2008 Stage 1, Grade 3, TNB, 1.7 cm tumor,Negative nodes TX partial masectomy, 4 rounds A/C, 4 rounds Abraxane
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krisa View Drop Down
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Post Options Post Options   Thanks (0) Thanks(0)   Quote krisa Quote  Post ReplyReply Direct Link To This Post Posted: Apr 13 2009 at 6:34pm
gerriesue,
i was hoping that if i could get into one of those difficult yoga poses, it would cancel out the peeps i have eaten. 
Smile
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Linda S View Drop Down
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Post Options Post Options   Thanks (0) Thanks(0)   Quote Linda S Quote  Post ReplyReply Direct Link To This Post Posted: Apr 13 2009 at 7:50pm
Has anyone heard from Denise and how she's doing after her bone marrow biopsy? I've checked but don't see anything yet.
Linda S
DX 5/08, A/Cx4,carboplatin, abraxane,bi-lateral mast
11/2008, 9 cm,21/22node positive.rad 5 wks; mets to mediastinum/lungs 4/09. Xeloda/Navilbine w/pending biopsy for skin mets.
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gerriesue View Drop Down
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Post Options Post Options   Thanks (0) Thanks(0)   Quote gerriesue Quote  Post ReplyReply Direct Link To This Post Posted: Apr 13 2009 at 8:20pm
krisa, I don't know if anything cancels out peeps. But the restorative yoga can help with stiffness and strength. Haven't heard from Denise. Hoping for the best.
57 yrs. old at DX Oct. 2008 Stage 1, Grade 3, TNB, 1.7 cm tumor,Negative nodes TX partial masectomy, 4 rounds A/C, 4 rounds Abraxane
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krisa View Drop Down
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Post Options Post Options   Thanks (0) Thanks(0)   Quote krisa Quote  Post ReplyReply Direct Link To This Post Posted: Apr 13 2009 at 9:38pm
linda,
denise was on facebook and survived the biopsy, painful as it was.
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Post Options Post Options   Thanks (0) Thanks(0)   Quote dmwolf Quote  Post ReplyReply Direct Link To This Post Posted: Apr 13 2009 at 11:01pm
Hi, guys.  Thanks for thinking of me!  That makes me feel so cared for, that you were checking on me.  Well, I had the marrow slurpage, and no she did not smear it on bread (or matza) and eat it.  In fact, I didn't even see the vials she filled.  If I were a conspiracy theorist, I might suspect she gathered nothing, and is merely a sadist.  OOOh fun let's stick needles into people's bones.  The lidocaine burned like H-E-double tootpicks, for starters.  Then the whole drill in or whatever it was and slurp all, all highly unpleasant, even with my two sisters Ativan and Vicodin humming nicely in my veins.  Maybe they took the edge off, though not much.  After it was over we stopped by for falafels and drove home, where I slept for hours in a druggy haze.  All I needed was some crack friends to nod with.  Eventually I roused myself, visited with a friend, and then Joel and I went to see Leonard Cohen in concert.  It was fabulous, though I'm still a tad dopey and my lower back has been happier.   Now the scary part - waiting for results, and then getting them.  I should hear by sometime Wed, the same day I'll be doing a PetCT.  So, by day's end Wed I should know what is up in the Wolf body.  I'm hoping (against hope?) that the answer is a big, bleedin' nothing.  Happy, healthy body with tumor markers rising for no cancer-related reason.  Hope, hope...

Love,
Denise
DX 2/08@43 stg II IDC; gr2,0 nodes. Neoadj chemo, first ACx2 (fail) then CarboTaxotereX6(better). Lump, Rads done 11/08; Clodronate. False alarm queen: PetCT lung & TM marker. NED. PBM w/recon 9/10.
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trip2 View Drop Down
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Post Options Post Options   Thanks (0) Thanks(0)   Quote trip2 Quote  Post ReplyReply Direct Link To This Post Posted: Apr 14 2009 at 12:19pm
Denise good to hear from you, haven't been in fb in a few days, need to get over there.  I am so happy you made it thru and ended up having a nice day.  The procedure does sound very scary.
 
I have to ask, what is a falafels?
 
Okie dokie will be watching from a post from you soon saying everything A-OK!
Hug
Stage 2 2003
Stage 1 2007
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krisa View Drop Down
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Post Options Post Options   Thanks (0) Thanks(0)   Quote krisa Quote  Post ReplyReply Direct Link To This Post Posted: Apr 14 2009 at 12:25pm
pam,
falafels cancel out peeps.

Wink

denise....waiting with you; waiting with everyone on this forum that is waiting to hear something.

Heart


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trip2 View Drop Down
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Post Options Post Options   Thanks (0) Thanks(0)   Quote trip2 Quote  Post ReplyReply Direct Link To This Post Posted: Apr 14 2009 at 12:30pm
Oh cool!  I don't think they've ever heard of them around here, actually I could bet on that.  Google here I come.Cool
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Post Options Post Options   Thanks (0) Thanks(0)   Quote Linda S Quote  Post ReplyReply Direct Link To This Post Posted: Apr 14 2009 at 4:09pm
Thanks everyone for a good laugh. The whole business about peeps and now falafel! You ladies are toooooooo funny. Denise, so glad you maintain your sense of humor through something so awful. Your courage and humor are inspiring. Prayers for good results!
Linda S
DX 5/08, A/Cx4,carboplatin, abraxane,bi-lateral mast
11/2008, 9 cm,21/22node positive.rad 5 wks; mets to mediastinum/lungs 4/09. Xeloda/Navilbine w/pending biopsy for skin mets.
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trip2 View Drop Down
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Post Options Post Options   Thanks (0) Thanks(0)   Quote trip2 Quote  Post ReplyReply Direct Link To This Post Posted: Apr 14 2009 at 4:12pm
Linda how are you doing?
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Stage 1 2007
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Linda S View Drop Down
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Post Options Post Options   Thanks (0) Thanks(0)   Quote Linda S Quote  Post ReplyReply Direct Link To This Post Posted: Apr 14 2009 at 4:22pm
Met with my onc today. He said since the cancer has metastized, there is no curing it, but he will try to get it into remission. Starting me on Xeloda (it's pill form and since my husband and I are planning a trip along the Pacific shore, I can take it on the road). We also discussed Ixempra. He said combining the two would give me no quality of life, so he's being conservative that way. Also wants to try PARP inhibitors? Still haven't googled that one but will tonight. He still says the average life expectency is about one year after known mets, but at least we're still fighting. I read something in one of the forums/threads, and the author and location is escaping me at the moment, but it was a post about the mean/average (written by a professor who had mesothelioma). That article reminds me that we are not 'average' and there are always those that beat the odds. Too bad it can't be all of us?
Linda S
DX 5/08, A/Cx4,carboplatin, abraxane,bi-lateral mast
11/2008, 9 cm,21/22node positive.rad 5 wks; mets to mediastinum/lungs 4/09. Xeloda/Navilbine w/pending biopsy for skin mets.
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Post Options Post Options   Thanks (0) Thanks(0)   Quote BrendaF Quote  Post ReplyReply Direct Link To This Post Posted: Apr 14 2009 at 4:32pm
Linda, I read that, too.  I believe it was a link that Zenrookie posted in the NoSurrender forum.
 
BTW, I'm now 17 months out from mets dx.
Dx 2005 2 cm, 5/12 nodes, A/C + T, 28 rads.
Dx mets 12/07 mediastinal and supraclavicular nodes, carbo + taxotere X 6.
brain, lymph, pleura, bone mets. Started Xeloda 8/24/09
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