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Old 09-26-2010, 04:37 PM   #1
sally
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Spreading

Hi Everone. The last thread I started erased all of the responses. I'm not sure why. Anyway, I finished my 18 WBR treatments and had my first taxol, cisplatin, and herceptin treatment 4 days after my last rad. I will be getting this combo weekly. I'm not sure about the Herceptin, if it's weekly or every 3 weeks. I get my second one Wednesday. I have been extremely tired and my head and ears are burned. The back of my throat and mouth feel stripped and burnt. I have severe dry mouth. I have been using toothpaste for dry mouth and Biotene for rinse. Any othe suggestions. Thnks again for all he other information. Sally
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Dx March 2004 HER2+ er/pr+ 8/16 + lymphnodes mets to the liver Stage IV / 6 cycles of TCH and 33 rads . NED Continued Herceptin 3 years w/ Femara. Tumor markers start to rise in Jan of 2007 and swiched to Tamoxifen. August of 2007 found more mets to liver and lymphnodes outside of liver. Went on Tykerb/Xeleoda--spots on liver gone found large mass between intestines. March 2008 started TCH. Stopped Carboplatin due to allergy. Still on Taxotere and Herceptin. Nov 2008 mass is gone. 3 new spot on liver and one on spine. Radiation on spine. tykerb/gemzar for liver mets. PET in April 09 showed shrinkage still a little activity, continue tykerb/gemzar until Aug 09. PET showed new spot on my spine more on my liver and a bunch of enlarged lymphnodes in upper chest. Start Adriamycin Sep 09. more radiation on spine . April 2010- Still on Adriamycin 3wks on 1 wk off and zometa every 28 days. PET -May 2010 showed progression. Starting Herceptin/Navelbine on June '10
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Old 09-26-2010, 05:35 PM   #2
StephN
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Re: Spreading

Dear Sally -
You are in the thick of it now. The chemos are hard on the mouth and throat. I also used the Biotene products, but found something called ULCER EASE that worked great for my mouth.

I would suggest apple sauce, soft boiled eggs with soda crackers, scrambed eggs or omelets, mild soups (not the salty ones from the store in cans) with rice or small noodles, cheese toast, fresh fruits.

The Cisplatin is tough. All the best for a good result, so you can eliminate that one.
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MY STORY SO FAR ~~~~
Found suspicious lump 9/2000
Lumpectomy, then node dissection and port placement
Stage IIB, 8 pos nodes of 18, Grade 3, ER & PR -
Adriamycin 12 weekly, taxotere 4 rounds
36 rads - very little burning
3 mos after rads liver full of tumors, Stage IV Jan 2002, one spot on sternum
Weekly Taxol, Navelbine, Herceptin for 27 rounds to NED!
2003 & 2004 no active disease - 3 weekly Herceptin + Zometa
Jan 2005 two mets to brain - Gamma Knife on Jan 18
All clear until treated cerebellum spot showing activity on Jan 2006 brain MRI & brain PET
Brain surgery on Feb 9, 2006 - no cancer, 100% radiation necrosis - tumor was still dying
Continue as NED while on Herceptin & quarterly Zometa
Fall-2006 - off Zometa - watching one small brain spot (scar?)
2007 - spot/scar in brain stable - finished anticoagulation therapy for clot along my port-a-catheter - 3 angioplasties to unblock vena cava
2008 - Brain and body still NED! Port removed and scans in Dec.
Dec 2008 - stop Herceptin - Vaccine Trial at U of W begun in Oct. of 2011
STILL NED everywhere in Feb 2014 - on wing & prayer
7/14 - Started twice yearly Zometa for my bones
Jan. 2015 checkup still shows NED
2015 Neuropathy in feet - otherwise all OK - still NED.
Same news for 2016 and all of 2017.
Nov of 2017 - had small skin cancer removed from my face. Will have Zometa end of Jan. 2018.
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Old 09-27-2010, 01:55 AM   #3
tricia keegan
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Re: Spreading

Hi Sally,

Sorry you have this problem, I got a tip which worked for me when I had mouth ulcers/dry mouth during chemo. I was told to freeze cranberry juice and make small ice cubes of them which I sucked on before eating, it did'nt cure it but did make things easier
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Dx July '05 IDC 1.9cm Triple positive 3/9 nodes positive
A/C X 4 ..Taxol/Herceptin x 12 wks then herceptin 1 yr
Rads x 36 ..oophorectomy August '06
Currently taking Arimidex..
June 2011 osteopenia/ zometa x1 yearly- stopped Zometa 2015 as Dexa show normal bone density.
Stopped Arimidex July 2014- Restarted Arimidex 2015 for a further two years on the advice of my Onc.
2014 Normal Dexa scan
2018 Mammo all clear, still NED!
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Old 09-27-2010, 04:22 PM   #4
krisvell
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Re: Spreading

Sally,
I am praying your latest treatments will beat the beast back into non-existence.

Kris...
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06/08/09 - 55, IDC, IIIA, ER+/PR-/HER+++
Nottingham 6/9 - Grade 2 5.2cm, several nodes
06/23/09 - Neoadjuvant - TCH Herceptin til June
10/07/09 - Finished Chemo
10/27/09 - Mastectomy RB
Path Report: RB No residual tumor pCR,
2 of 15 pos - .5mm largest micromets
12/18/09 - Radiation started (28)
02/05/10 - Finished Radiation
01/11/10 - Started Femara
06/22/10 - Finished Herceptin.. My son's 22nd BD. Hope it's a sign! Hoping for the best.
11/15/10 - Started Walter Reed BC Vaccine trial at
1/04/11 - Sibley Mem. Had to withdraw due to met
01/23/11 - Stage IV - Brain Met 1.6cm 1.7cm
02/03/11 - Gamma Knife (2 fracts to minmize necrosis)
03/01/11 - Gamma Knife
6/11 - Necrosis
7/11 - Necrosis stopped & Tumor progression
8/11 = Now think it's really necrosis
9/11 - Avastin every two weeks -- It's working!! Necrosis is shrinking.
12/11 - Necrosis gone AVASTIN worked.
12/11 - Bone &CT found


Oct '10 - Ran Hartford 1/2 Marathon to Thank Dr. Slamon for Herceptin!
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Old 09-27-2010, 05:48 PM   #5
Jackie07
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Re: Spreading

Sally,

If you click on your name by your posting, you can view your past threads/posts. I think your 'old' thread is still there:

http://her2support.org/vbulletin/showthread.php?t=46759

As for the dry mouth, I can only suggest to increase you fluid intake. Do you chew ice while getting the infusion? I remember being given ice during certain chemo sessions. The WBR probably has also caused more fatigue and dryness.

Are you following the 1 tsp salt + tiny baking soda + 8 oz. water procedure and gargle after meals and before bed time? Do report problems to your oncology nurse so he/she can take care of it right away. I'm not sure about the toothpaste. Seemed it was too strong for me to use during chemo. There were a couple of threads discussing about prevention/treatment of mouth sores. You might want to do a 'search' and read about the tips offered there.
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Last edited by Jackie07; 09-27-2010 at 05:50 PM..
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Old 09-27-2010, 06:10 PM   #6
Laurel
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Re: Spreading

I have no further suggestions for the dry mouth and discomforts from your treatment. I just wanted you to know I am so sorry to hear you are suffering and pray this will be effective at getting you back to NED, so it will all be worth the torture!
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Smile On!
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Dx'd w/multifocal DCIS/IDS 3/08
7mm invasive component
Partial mast. 5/08
Stage 1b, ER 80%, PR 90%, HER-2 6.9 on FISH
0/5 nodes
4 AC, 4 TH finished 9/08
Herceptin every 3 weeks. Finished 7/09
Tamoxifen 10/08. Switched to Femara 8/09
Bilat SPM w/reconstruction 10/08
Clinical Trial w/Clondronate 12/08
Stopped Clondronate--too hard on my gizzard!
Switched back to Tamoxifen due to tendon pain from Femara

15 Years NED
I think I just might hang around awhile....

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