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Old 06-22-2008, 09:04 PM   #1
ElaineM
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Sad news

I am so sorry to hear the sad news. My sympathies to her family and friends.
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Peace,
ElaineM
12 years and counting
http://her2support.org/vbulletin/showthread.php?t=48247
Lucky 13 !! I hope so !!!!!!
http://her2support.org/vbulletin/showthread.php?t=52807
14 Year Survivor
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"You never know how strong you are until being strong is the only choice you have." author unknown
Shared by a multiple myeloma survivor.
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Old 06-23-2008, 04:49 PM   #2
Andrea Barnett Budin
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Location: LAND OF YES! w/home in Boca Raton, Florida Orig from L.I., N.Y. Ever hovering IN THE NOW...
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Sending Hugs And Love...

I understand. It is hard not to identify. It is a tragic loss for so many.

When Dana, Christopher Reeve's suddenly died of lung cancer, I immediately called my dear friend in Chicago. She is now 4 yrs out from her initial lung dx. I told her, I know what you are thinking, but don't go there. This was an unusual and catastrophic experience. Of course she tried her best but inexplicably such shocking things can occur. To anyone, at any time.

I pray Belinda that you and those who have admired Jane so throughout the years will make peace with this sad turn of events. I send my deepest condolences. Our heroes and sheroes mean the world to us. Sending love and hugs,
Andi
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'95 post-meno dx Invasive LOBULAR w/9cm tumor! YIKES + 2/21 nodes. Clear mammo 10 mnths earlier. Mastec/tram flap reconst/PORT/8 mnths chemo (4Adria/8CMF). Borderline ER/PR. Tamoxifen 2 yrs. Felt BLESSED. I could walk and talk, feed and bathe myself! I KNEW I would survive...

'98 -- multiple mets to liver. HER2+ 80%. ER/PR- Raging, highly aggressive tumors spreading fast. New PORT. 9 mnths Taxotere Fought fire w/fire! Pronounced in cautious remission 5/99. Taxotere weekly for 6 wks, 2 wks off -- for 9 mnths. TALK ABOUT GRUELING! (I believe they've altered that protocol since those days -- sure hope so!!)
+ good old Vit H wkly for 1st 3 yrs, then triple dosage ev 3 wks for 7 yrs more... The "easy" chemo, right?! Not a walk in the park, but not a freight train coming at 'ya either...

Added Herceptin Nov '98 (6 wks after FDA fast-tracked it for met bc). Stayed w/Vit H till July '08! Now I AM FREE! Humbly and eternally grateful for this life-saving drug! NED since '99 and planning on keeping it that way. To hell w/poor prognosis and nasty stats! STOPPED VIT H JULY '08...! REMAIN STABLE... Eternally grateful...Yes is a world & in this world of yes live (skillfully curled) all worlds ... (e e cummings) EVERY DAY I BEAT MY PREVIOUS RECORD FOR # OF CONSECUTIVE DAYS I'VE STAYED ALIVE. Smile KNOWING you too can be a miracle. Up to me and God now...

Last edited by Andrea Barnett Budin; 06-23-2008 at 04:50 PM.. Reason: strange symbols that don'
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Old 06-24-2008, 08:19 PM   #3
Roz
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Location: Sydney Australia
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Jane McGrath

We are all feeling sad after Jane's death. It brings death so much closer to us as individuals. Becky, Jane was diagnosed in 1997, but did not have a recurrence until 2002. She and her well known husband appeared on a popular chat show in 2004 (I think that was the year) and she came across as a warm, funny and courageous person, as did her husband. Her funeral is today, and $200,000 have been donated by the Australian public to her foundation since her death last week. I fel very sad for all her loved ones and for her death at such a young age.
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diagnosed June 03. Rt sided Inflammatory BC in rt lower quadrant. 7cm tumour. Also 3 DCIS. 3 rounds of EC, mastectomy with axillary clearance (12 nodes+ of 19). 1 more EC. 5 weeks of rads, with weekly booster to attack skin lymph involvement. 4 cycles of Taxol. Tamoxifen.Recurrence December 04, Herceptin started early Jan05,+ Arimidex.
NED 26 mths. Recurrence early Mar07. Taxol added to Herceptin. NED. Will have total of 6 cycles, then Aromisan and Herceptin. Early Oct 07, recurrence to the pesky right upper lobe, with some pleural thickening upper rt hemithorax. T/X now the treatment. May 2008, Taxatere and Herceptin for lung recurrence
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