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Old 08-22-2007, 08:15 AM   #1
StillHere
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Location: Greendale, WI just outside Milwaukee
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Lightbulb Gift of love to Marie (Believe 51)

Hey all, It is hard to believe that Marie just joined this group in June of this year. I feel I have always known her through her heartfelt and inspirational posts. I had an idea I want to share w/ you. I think Marie would really benefit from a SPA outing in Jan or Feb 2008. I think we could swing this for her if we each donated $10.00 or more. I think she is in dire need of real flesh and blood hugs and this would be the perfect time to provide our healing touch to her. I will start the ball rolling by sending a $25.00 donation to be ear marked for Marie to attend our winter outing to:

Marie (Believe51 SPA fund)
Her 2 Support Group Org.
6973 Mimosa Drive
Carlsbad, CA 92009-5156

Joe & Christine - I did not check w/ you first, but I am hoping this can be done. I understand this fund will not be tax deductible - just a gift from the heart to a close friend.
__________________
04/05 Onset 49, DCIS, solid, Hist 2/3, Nucl 2/3, 7cm R Brst
04/05 E & P + HER2+++
05/05 Mediport
05/05 Cytoxan & Adriamycin every 3wk x4
08/05 Taxol every 2wk x 4, Herceptin every wk x1yr
10/05 Bilat Mast - my Choice
10/05 3/19 lymph nodes Pos, Stage IIIa
11/05 Rad x 37 Rx, R Brst & Axcilla
02/06 Herceptin stopped (L vent HF 40)
03/06 Started & Stoped Arimidex after 2 mos.-QOL side effects
05/06 Started Tamoxafin
06/06 Bilat Free Flap Reconstruction
12/06 Cardiomyopathy reversed-HF normal
01/07 Bilat Saline Implants
07/07 CA 27-29 steadily rising from 28 in 12/06 to 46 in 7/07
07/07 PET Scan NED, but inflamation at prev surg site.
09/07 Started Femara
10/07 CA 27-29 down to 39
06/08 CA 27-29 down to 32
09/08 Lg joint pain & QOL side effects from Femara, will live w/ to keep CA markers within normal range.
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Old 08-22-2007, 08:37 AM   #2
VaMoonRise
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Smile Awesome Idea!!!!!!

What an awesome idea!!! I am soooooo glad that you thought of this and ashamed that I didn't think of it first, lol.

My check is on it's way! And to make up for not thinking of it first I will raise your $25 and send $50, lol. Anyone else up to the challenge that I just threw down? lol.

Love you guys sooooooo much, not only are you such Magnificent Courageous Warriors but you truly are Angels here on earth. I am so very proud to call you all Sisters and to be a part of such a wonderful group. I can't begin to thank Christine & Joe enough for starting this tremendous web site (The best BC support group on the web, hands down) and for bringing us all together.

Love, Hugs & God Bless to all of You!
Nicola

__________________



March 18, 2004, Age 36
Diagnosed: High Grade DCIS, Microcalcifications, Solid and Comedo type, Nuclear grade 3 with 1mm margins, ER+, PR+, Stage "0"
3-8-04 Left breast lumpectomy.
4-1-04 thru 6-24-04 Adjuvant XRT.
11-29-05 Gallbladder attack.
12-01-05 Surgery to have gallbladder removed, discovered cancer spread throughout liver in both lobes, HER2+ amplified by FISH and interestingly enough negative for ER and PR.
12-9-05 Clinical trial consisting of Tykerb, Taxol and Herceptin along with Zometa once a month. On clinical trial for 15 months before liver mets started progressing. Started on Navelbine 3-9-07. Navelbine failed, switched to Gemzar July 07. MRI of the brain on July 7, 07. Results revealed multiple brain tumors. Taken off of Gemzar immediately and began 15 rounds of WBR which I completed on July 26, 07. CT scan on 7-26-07 significant progression in the liver mets. I am now getting ready to start on Xeloda along with Herceptin and Zometa once a month.
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Old 08-22-2007, 10:12 AM   #3
Joe
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I would prefer that someone volunteer to handle this fund. Christine and I will be extremely busy until after the first of the year and I don't need the additional work.

Regards
Joe
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Old 08-22-2007, 10:34 AM   #4
StillHere
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Joe
So sorry, I would be happy to set up a fund. I just wanted to make sure everyone knew that this is above board and not a scam of any kind. My check is already in the mail, so please just tear it up when you receive it. Please send checks to:

Karen Schneck for Marie Fund
7201 Devonshire Ave
Greendale, WI 53129

I will collect donations and forward to Marie. Thank you
__________________
04/05 Onset 49, DCIS, solid, Hist 2/3, Nucl 2/3, 7cm R Brst
04/05 E & P + HER2+++
05/05 Mediport
05/05 Cytoxan & Adriamycin every 3wk x4
08/05 Taxol every 2wk x 4, Herceptin every wk x1yr
10/05 Bilat Mast - my Choice
10/05 3/19 lymph nodes Pos, Stage IIIa
11/05 Rad x 37 Rx, R Brst & Axcilla
02/06 Herceptin stopped (L vent HF 40)
03/06 Started & Stoped Arimidex after 2 mos.-QOL side effects
05/06 Started Tamoxafin
06/06 Bilat Free Flap Reconstruction
12/06 Cardiomyopathy reversed-HF normal
01/07 Bilat Saline Implants
07/07 CA 27-29 steadily rising from 28 in 12/06 to 46 in 7/07
07/07 PET Scan NED, but inflamation at prev surg site.
09/07 Started Femara
10/07 CA 27-29 down to 39
06/08 CA 27-29 down to 32
09/08 Lg joint pain & QOL side effects from Femara, will live w/ to keep CA markers within normal range.
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Old 08-22-2007, 10:49 AM   #5
kimber
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Great idea!! And Nicola - I will accept your challange and raise you! I am sending $75. My check is on it's way!

God bless you all - kim
__________________
dx 5-05 @42 years old
IDC stage IIA
ER+ (100%) ER+ (75%) HER2+
double mastectomy
4DD AC - 16 weekly Taxol
6 months Herceptin - stopped due to MUGA
35 chest wall rads
Tamoxifen
Lat flap with silicone implant reconstruction on left side due to radiation. "Normal" silicone on right. Finished all reconstruction 6-07!!!
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Old 08-22-2007, 12:49 PM   #6
StillHere
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I am starting to think no good deed goes unpunished. I just returned from my bank. Wanted to find out the logistics of starting this fund. It appears the easiest way to do this is just send checks directly to Marie. If you send them to me, you can rest assured that I will endorse them over to Marie.

Marie, can you share your last name on-line to help us help you?

Marie, Can you private email your address to me, so I can forward any funds sent to my address.

Everyone, I still think this can work, it is just a little more red tape than I expected. I sincerely hope that this snag in the procedure does not deter anyone from donating to our friend.
__________________
04/05 Onset 49, DCIS, solid, Hist 2/3, Nucl 2/3, 7cm R Brst
04/05 E & P + HER2+++
05/05 Mediport
05/05 Cytoxan & Adriamycin every 3wk x4
08/05 Taxol every 2wk x 4, Herceptin every wk x1yr
10/05 Bilat Mast - my Choice
10/05 3/19 lymph nodes Pos, Stage IIIa
11/05 Rad x 37 Rx, R Brst & Axcilla
02/06 Herceptin stopped (L vent HF 40)
03/06 Started & Stoped Arimidex after 2 mos.-QOL side effects
05/06 Started Tamoxafin
06/06 Bilat Free Flap Reconstruction
12/06 Cardiomyopathy reversed-HF normal
01/07 Bilat Saline Implants
07/07 CA 27-29 steadily rising from 28 in 12/06 to 46 in 7/07
07/07 PET Scan NED, but inflamation at prev surg site.
09/07 Started Femara
10/07 CA 27-29 down to 39
06/08 CA 27-29 down to 32
09/08 Lg joint pain & QOL side effects from Femara, will live w/ to keep CA markers within normal range.
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Old 08-22-2007, 02:00 PM   #7
Believe51
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Location: RHODE ISLAND (Ed getting me a latte on 2nd Cancerversary Cruise 2008) 'BELIEVE': To accept as true or real, To have faith in, To presume ALWAYS BELIEVE
Posts: 2,999
Talking You All Take My Breath Away

When I first read this post I was breathless, I could not find any words to express myself about my love for this family of mine. As you know I usually not at a loss for words and Nicola really has me running to save that reputation. LOL!! I had to read it over and over because I could not believe this was happening to little 'ole me. I originally joined this group in March of this year under the alias Marie G and after the computer hijack and the different course of hubby's journey I decided to start fresh with a strong, demanding name that would sum up this journey and who I am....and that is how Believe51 was born!!! LOL (the 51 was Ed's age when joining).

I am truely touched how this family has not only educated me, but how they have helped me to grow and attack cancer!! Your spirit and beauty have always helped me to become this warrior for my husband. Through the last several months I have taken great pride in all of my friends here and always follow their journeys in my mind daily. The prayers are always said, the positive energy always flows, the love will forever be everlasting, candles always burn with sweet thoughts of "My Girls". Probably something you do not know about me...I am territorial!! LOL. Each day I wake up and hear what is going on with my friends part of me wants to get into a car, bus, train, plane just to give a hug. Never did I think that you all know how I need those hugs too, that I have lived my life without you all and that makes me wonder HOW??

I shall always remain here close to heart with everyone and this is extremely important to my husband as well as for me. This is the only place I can come and be myself. My true self. As we know life is full of formalities and some things we have to hide. My post yesterday was a little sad and I asked you not to cry. How true it is to say that was an unreasonable request to ask from you all. When we are our 'true selves' and tell our stories they are pure, they are from the bottom of our souls.

Thank you for the gesture of kindness and support, I feel a bit guilty knowing that you are all living with cancer and you are concerned about me and my welfare. Little 'ole me!! (tears). You all here continue to rescue me from the darkest corners of our journey, you have softened every blow. Continually catching me before I fall and wiping off my knees. In my visualization of you Loves I feel you all wipe my tears and kiss my face. I watch you all recognize my feelings and accept me for the passionate person I am.

Thank you all for sharing this journey with us and for allowing us to join yours. The feelings that go along with cancer are sometimes personal, not here, not in our home!! I take pleasure loving you all. I am honored to have you all in my life. You all never cease to amaze me and you always shall. I am still besides myself and very speachless. Again, thank you for picking us up and giving us life. Cancer has potentially taken some time off the end of his life, but you have all given it back to us.

Thank You All For Being The Wind Beneath My Wings!!

I feel so much better than I did yesterday and that is all thanks to you, deeply indebited forever!! Our love for you all grow with each passing day!! How blessed we all are!!>>Believe51
__________________
9/7/06Husband 50yrs=StageIV IBC/HER2+,BoneMets10/06TaxotereX10,'H'1X wk,Zometa,Tamoxifen4/12/07Last Tax5/18/07Pet=Rapid Cell Activity,No Organ Mets,Lytic Lesions,Degeneration,Some Bone Repair5/07ChemoFail6/01/07Pleural Thoracentisis=Effusions,NoMalignantCells6/19/07+7/2/07DFCI
6/25/07BrainMRI=BrainMets,Many<9mm7/10/07WBR/PelvisRad37.5Gx15&Nutritionist8/19/07T/X9/20/07BrainMRI=2<2mm10/6/07Pet=BoneProgression
10/24/07ChemoFail11/9/07A/Cx10,EndTam12/7/07Faslodex12/10/07Muga7512/13/07BlasticLesions1/7/08BrainMRI=Clear4/1/08Pet=BoneImprovement,
NoProgression,Stable4/7/08BrainPerfect5/16/08Last A/C8/26/08BrainMets=10(<9mm)9/10/08Gamma10/30/08Met=5mm12/19/08Gamma5mets5
12/22/08SpinalMets1/14/09SpinalRads2/17/09BrainMRI=NoNewMets4/20/09BoneScan5/14/09Ixempra6/1/09BrainMRI=NumerousMets6/24/09DFCIw/DrBurstein6/26/09Continue
Ixempra/Faslodex/Zometa~TM now lower7/17/09Stop Ixempra By Choice9/21/09HOSPICE10/16/09Earned His Deserved Wings And Halo=37 Month Fight w/Stage 4 IBC, Her2+++,My Hero!!
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Old 08-22-2007, 05:15 PM   #8
Audrey
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Marie, I'm so glad to read that you are feeling happier today--isn't this the best website, with the most caring people? (Maybe that's why I can't seem to cut the cord more than six years after my initial diagnosis). Anyway, just wanted you to know that I'd be happy to contribute to your "spa fund"--you have such a way with words and expressing yourself that cuts right to the heart. Your husband is lucky to have you by his side during his cancer fight--don't give up hope, as you know--with God all things are possible.
__________________
Audrey

diagnosed July 2001, at age 36
large tumor, 11+ nodes
Stage IIIb, er/pr-, Her2+
treated with A/C, weekly Taxol
radiation, + year of Herceptin
on clinical trial. double mastectomy
followed by reconstruction
NED!!
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Old 08-22-2007, 09:35 PM   #9
Debra
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Count me in as well. This would be the best cause I have donated to all year!
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Debra

Diag. 11/05 at age 40 triple positive
3.8 cm tumor and 9 mm tumor
Stage IIb/SN positive(no other nodes)Grade 3
Bilat. mastect. 12/05 (Rt.prophylactic) followed with AC/taxol/Herceptin/tamoxifen then switched to arimidex after hysterectomy in 12/06. August 07 switched to Aromasin due to severe jt. pain from Arimidex. Nov. 2011 No more meds and NED!
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Old 08-23-2007, 05:40 PM   #10
StillHere
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Just to let you all know that Marie has sent me a private email with her name, address & phone #. If you don't feel comfortable sending the checks to me to endorse and forward to Marie, please private email me and I will send you the needed information. I think the generous donations are wonderful, but if everyone who regularly reads Marie's posts sent $5, or $10 it would add up very quickly. The Miraval sales rep is out of the office until Wed. 8/29. Hope to get some details of cost of this resort to you next week.
__________________
04/05 Onset 49, DCIS, solid, Hist 2/3, Nucl 2/3, 7cm R Brst
04/05 E & P + HER2+++
05/05 Mediport
05/05 Cytoxan & Adriamycin every 3wk x4
08/05 Taxol every 2wk x 4, Herceptin every wk x1yr
10/05 Bilat Mast - my Choice
10/05 3/19 lymph nodes Pos, Stage IIIa
11/05 Rad x 37 Rx, R Brst & Axcilla
02/06 Herceptin stopped (L vent HF 40)
03/06 Started & Stoped Arimidex after 2 mos.-QOL side effects
05/06 Started Tamoxafin
06/06 Bilat Free Flap Reconstruction
12/06 Cardiomyopathy reversed-HF normal
01/07 Bilat Saline Implants
07/07 CA 27-29 steadily rising from 28 in 12/06 to 46 in 7/07
07/07 PET Scan NED, but inflamation at prev surg site.
09/07 Started Femara
10/07 CA 27-29 down to 39
06/08 CA 27-29 down to 32
09/08 Lg joint pain & QOL side effects from Femara, will live w/ to keep CA markers within normal range.
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Old 08-23-2007, 07:01 PM   #11
dorinda
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I Would Love To Be Apart Of This Adventure For Marie. I Have Grown From Just Reading Her Post. Everything She Has Expressed I Have Felt Through My Bc Journey.thanks For Letting Me Be Apart Of This. Dorinda
__________________
nov 2006 dx. with bc. 3 tumors removed from left breast lumpectomy done. her2 postive er+pr-. scans showed extensive spine mets(to many to count) ,3 tumors on left rib,one tumor on skull and 3 tumors on liver. stage IV from get go. dec.2006 started chemo taxol and herceptine wkly. zometa monthly. rescanned in march 2007, liver tumors shrinking a little. bones to early to tell but pain is gone in my back. rescanned in june 2007. liver mets gone, bone scan looking better but still alot in my spine. still on taxol and herceptine. zometa monthly. rescanned in august due to ca 2729 going up. liver still good , mets in ribs and skull gone but multiple areas still on lumbar and sacrum. mri of brain august 07 negative for mets.I AM BELIEVLING GOD FOR MY HEALING.
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Old 08-24-2007, 09:45 AM   #12
Believe51
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Location: RHODE ISLAND (Ed getting me a latte on 2nd Cancerversary Cruise 2008) 'BELIEVE': To accept as true or real, To have faith in, To presume ALWAYS BELIEVE
Posts: 2,999
Talking One More Time

I say one more time that I cannot believe this is happening to 'lil ole me. I ask anyone who will be donating to private e-mail me with your address, I will need them for my letters. I still feel a bit shy (for lack of better words) about the whole thing and still at a loss for words (I know, I know..me at a loss for words!) I guess I am so used to doing the giving in my life that it is strange to recieve sometimes. You are all my heros and I cannot believe I will be a part of this great adventure. Waiting for the hugs!!>>Believe51
__________________
9/7/06Husband 50yrs=StageIV IBC/HER2+,BoneMets10/06TaxotereX10,'H'1X wk,Zometa,Tamoxifen4/12/07Last Tax5/18/07Pet=Rapid Cell Activity,No Organ Mets,Lytic Lesions,Degeneration,Some Bone Repair5/07ChemoFail6/01/07Pleural Thoracentisis=Effusions,NoMalignantCells6/19/07+7/2/07DFCI
6/25/07BrainMRI=BrainMets,Many<9mm7/10/07WBR/PelvisRad37.5Gx15&Nutritionist8/19/07T/X9/20/07BrainMRI=2<2mm10/6/07Pet=BoneProgression
10/24/07ChemoFail11/9/07A/Cx10,EndTam12/7/07Faslodex12/10/07Muga7512/13/07BlasticLesions1/7/08BrainMRI=Clear4/1/08Pet=BoneImprovement,
NoProgression,Stable4/7/08BrainPerfect5/16/08Last A/C8/26/08BrainMets=10(<9mm)9/10/08Gamma10/30/08Met=5mm12/19/08Gamma5mets5
12/22/08SpinalMets1/14/09SpinalRads2/17/09BrainMRI=NoNewMets4/20/09BoneScan5/14/09Ixempra6/1/09BrainMRI=NumerousMets6/24/09DFCIw/DrBurstein6/26/09Continue
Ixempra/Faslodex/Zometa~TM now lower7/17/09Stop Ixempra By Choice9/21/09HOSPICE10/16/09Earned His Deserved Wings And Halo=37 Month Fight w/Stage 4 IBC, Her2+++,My Hero!!
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Old 08-25-2007, 12:01 PM   #13
StillHere
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Location: Greendale, WI just outside Milwaukee
Posts: 211
Update-First check came in the mail today. Here we go, let's get Marie on this SPA outing where ever it may be.
__________________
04/05 Onset 49, DCIS, solid, Hist 2/3, Nucl 2/3, 7cm R Brst
04/05 E & P + HER2+++
05/05 Mediport
05/05 Cytoxan & Adriamycin every 3wk x4
08/05 Taxol every 2wk x 4, Herceptin every wk x1yr
10/05 Bilat Mast - my Choice
10/05 3/19 lymph nodes Pos, Stage IIIa
11/05 Rad x 37 Rx, R Brst & Axcilla
02/06 Herceptin stopped (L vent HF 40)
03/06 Started & Stoped Arimidex after 2 mos.-QOL side effects
05/06 Started Tamoxafin
06/06 Bilat Free Flap Reconstruction
12/06 Cardiomyopathy reversed-HF normal
01/07 Bilat Saline Implants
07/07 CA 27-29 steadily rising from 28 in 12/06 to 46 in 7/07
07/07 PET Scan NED, but inflamation at prev surg site.
09/07 Started Femara
10/07 CA 27-29 down to 39
06/08 CA 27-29 down to 32
09/08 Lg joint pain & QOL side effects from Femara, will live w/ to keep CA markers within normal range.
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Old 09-06-2007, 04:34 PM   #14
StillHere
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Angry Not the response I was hoping for

I have been waiting for a few more checks to arrive before forwarding them off to Marie. I am sorry to report that so far I will only be forwarding 3 checks. (Joe, I did get the check I originally sent to you back in the mail. - Thanks). I will wait til Monday 9/10 to mail the checks in case anyone else wants to contribute and forgot. I hope some of you just bypassed me and sent a gift directly to Marie. I realize this is not a life or death cause to contribute to, but I guess I was naive enough to think there would be a much greater outpouring of support for our cyber friend and wonderful caregiver. OK, I'm done. Peace - Karen
__________________
04/05 Onset 49, DCIS, solid, Hist 2/3, Nucl 2/3, 7cm R Brst
04/05 E & P + HER2+++
05/05 Mediport
05/05 Cytoxan & Adriamycin every 3wk x4
08/05 Taxol every 2wk x 4, Herceptin every wk x1yr
10/05 Bilat Mast - my Choice
10/05 3/19 lymph nodes Pos, Stage IIIa
11/05 Rad x 37 Rx, R Brst & Axcilla
02/06 Herceptin stopped (L vent HF 40)
03/06 Started & Stoped Arimidex after 2 mos.-QOL side effects
05/06 Started Tamoxafin
06/06 Bilat Free Flap Reconstruction
12/06 Cardiomyopathy reversed-HF normal
01/07 Bilat Saline Implants
07/07 CA 27-29 steadily rising from 28 in 12/06 to 46 in 7/07
07/07 PET Scan NED, but inflamation at prev surg site.
09/07 Started Femara
10/07 CA 27-29 down to 39
06/08 CA 27-29 down to 32
09/08 Lg joint pain & QOL side effects from Femara, will live w/ to keep CA markers within normal range.
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Old 09-11-2007, 09:08 AM   #15
StillHere
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Posts: 211
Thank you for your donations. The checks are in the mail today. Karen
__________________
04/05 Onset 49, DCIS, solid, Hist 2/3, Nucl 2/3, 7cm R Brst
04/05 E & P + HER2+++
05/05 Mediport
05/05 Cytoxan & Adriamycin every 3wk x4
08/05 Taxol every 2wk x 4, Herceptin every wk x1yr
10/05 Bilat Mast - my Choice
10/05 3/19 lymph nodes Pos, Stage IIIa
11/05 Rad x 37 Rx, R Brst & Axcilla
02/06 Herceptin stopped (L vent HF 40)
03/06 Started & Stoped Arimidex after 2 mos.-QOL side effects
05/06 Started Tamoxafin
06/06 Bilat Free Flap Reconstruction
12/06 Cardiomyopathy reversed-HF normal
01/07 Bilat Saline Implants
07/07 CA 27-29 steadily rising from 28 in 12/06 to 46 in 7/07
07/07 PET Scan NED, but inflamation at prev surg site.
09/07 Started Femara
10/07 CA 27-29 down to 39
06/08 CA 27-29 down to 32
09/08 Lg joint pain & QOL side effects from Femara, will live w/ to keep CA markers within normal range.
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Old 09-11-2007, 09:59 AM   #16
sherri
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Posts: 329
Hi Karen,

I got her address and sent it directly to her. Mail from Canada to US takes a long time, I don't know why. Maybe others also sent it to her.

Big hug,
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Old 09-11-2007, 05:55 PM   #17
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...
Posts: 1,904
Wink The Check Is In The Mail

I sent a check directly to Marie, the ANGEL that blesses this site and deserves Life's best!! Maybe others have done the same. I sure hope so. Let's give Marie (the world's greatest caregiver with a heart of gold and a passion and belief system that GLOW) a break. I put heaps of love in my envelope as well, along with big hugs and kisses. For both cheeks!
ANDI
__________________
Andi BB
'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...
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Old 09-11-2007, 06:46 PM   #18
kareneg
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Join Date: Nov 2005
Location: Lincoln, Rhode Island
Posts: 371
Hi Karen,

I hope you recieved my check I sent it over a week or so ago.
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Love and Hope
Karen

IDC
DX 1998 STAGE I ER+/ PR+
AC CHEMO TILL FEB 1999
Tamxofin till 2001
2001 exstensive liver mets and mets to lungs
Started weekly taxol
Jan 2002 found out I was strongly HER2POS+++ started herceptin continued with taxol and herceptin till June 2002 then from June 2002 till Jan 2005 just herceptin and Arimidex
2005 Navelbine herceptin had RFA Then back on taxol with herceptin
April 2006 progression again went on clinical trial with tykrerb/herceptin progressed on the started Xeloda/ herceptin
Feb 2007 started Doxil
August 2007 Taxotere,Carboplatin and Herceptin exstensive mets to liver and pancreas
October 2007 Had to stop Carboplatin due to sever allergic reaction
Jan 2008
Stopped Taxotere due to progression now on Gemzar and Herceptin
March 2008 Starting Carboplatin, Abraxane, and Herceptin.
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Old 09-11-2007, 08:02 PM   #19
StillHere
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Join Date: Mar 2007
Location: Greendale, WI just outside Milwaukee
Posts: 211
Karen,
Yes, I endorsed and forwarded it to Marie today. Thank you. KS
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04/05 Onset 49, DCIS, solid, Hist 2/3, Nucl 2/3, 7cm R Brst
04/05 E & P + HER2+++
05/05 Mediport
05/05 Cytoxan & Adriamycin every 3wk x4
08/05 Taxol every 2wk x 4, Herceptin every wk x1yr
10/05 Bilat Mast - my Choice
10/05 3/19 lymph nodes Pos, Stage IIIa
11/05 Rad x 37 Rx, R Brst & Axcilla
02/06 Herceptin stopped (L vent HF 40)
03/06 Started & Stoped Arimidex after 2 mos.-QOL side effects
05/06 Started Tamoxafin
06/06 Bilat Free Flap Reconstruction
12/06 Cardiomyopathy reversed-HF normal
01/07 Bilat Saline Implants
07/07 CA 27-29 steadily rising from 28 in 12/06 to 46 in 7/07
07/07 PET Scan NED, but inflamation at prev surg site.
09/07 Started Femara
10/07 CA 27-29 down to 39
06/08 CA 27-29 down to 32
09/08 Lg joint pain & QOL side effects from Femara, will live w/ to keep CA markers within normal range.
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Old 09-19-2007, 12:39 PM   #20
Believe51
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Join Date: Jun 2007
Location: RHODE ISLAND (Ed getting me a latte on 2nd Cancerversary Cruise 2008) 'BELIEVE': To accept as true or real, To have faith in, To presume ALWAYS BELIEVE
Posts: 2,999
Smile I am speechless

To my surprise I came home to a beautiful card with some donations for the spa-fund that Karen set up for me. I can still say I am speechless about the whole thing and a tad bit shy. I know, I know....SHY??..Marie is that you???

I cannot express my deepest heartfelt thanks for even thinking of me. At first, like I said I did not know how to react. This has to be one of the nicest things anyone has ever done for me and my life is full of riches. You girls are the most amazing group of friends ever and in a sense I do not feel 'worthy'. So many more of you need to go to the spa, so many of you need it more than me. But here you all are donating for me to go, how absolutely unselfish of you!!

I want to thank everyone who has donated for my cause (even if I do not think I am worthy!!). I want to thank you for feeling that I am worthy and making me realize what I mean to you!! How generally gracious you all are to think of me as needing this retreat. I am honored by the love I recieve here and quite proud to call you all 'My Greatest Love's"!! When I told Ed about this (fighting off tears) he too was speechless. I told him I would only go if he was feeling better. His reply: "Whether I am feeling good or not you are going. I will MAKE you go!!" This is really funny coming from a man who has never made me do anything. He does not even ask anything from me, except for maybe..."Are you doing laundry today??"

So with those tears still in my eyes I once again say thank you from the bottom of my very full heart. You all are my inspiration, my support, my deepest true loves. This family has the wonderful ability to fill us with the gifts that we never knew we were lacking. I still will never know where my husband and myself would be without you all. The greatest gift of all: Your loving friendship, it is priceless and with it I consider us COMPLETE!!

With Love and ultimate thanks>>Believe51

PS: Not only getting me to go to the spa, you are giving him a break from me!!! I am sure he will be relaxing knowing not just that I am gone, but that I will be spending quality time getting those "flesh & blood" hugs. I cannot wait to hold you all in my arms and whisper exactly what you mean to me!!!!
__________________
9/7/06Husband 50yrs=StageIV IBC/HER2+,BoneMets10/06TaxotereX10,'H'1X wk,Zometa,Tamoxifen4/12/07Last Tax5/18/07Pet=Rapid Cell Activity,No Organ Mets,Lytic Lesions,Degeneration,Some Bone Repair5/07ChemoFail6/01/07Pleural Thoracentisis=Effusions,NoMalignantCells6/19/07+7/2/07DFCI
6/25/07BrainMRI=BrainMets,Many<9mm7/10/07WBR/PelvisRad37.5Gx15&Nutritionist8/19/07T/X9/20/07BrainMRI=2<2mm10/6/07Pet=BoneProgression
10/24/07ChemoFail11/9/07A/Cx10,EndTam12/7/07Faslodex12/10/07Muga7512/13/07BlasticLesions1/7/08BrainMRI=Clear4/1/08Pet=BoneImprovement,
NoProgression,Stable4/7/08BrainPerfect5/16/08Last A/C8/26/08BrainMets=10(<9mm)9/10/08Gamma10/30/08Met=5mm12/19/08Gamma5mets5
12/22/08SpinalMets1/14/09SpinalRads2/17/09BrainMRI=NoNewMets4/20/09BoneScan5/14/09Ixempra6/1/09BrainMRI=NumerousMets6/24/09DFCIw/DrBurstein6/26/09Continue
Ixempra/Faslodex/Zometa~TM now lower7/17/09Stop Ixempra By Choice9/21/09HOSPICE10/16/09Earned His Deserved Wings And Halo=37 Month Fight w/Stage 4 IBC, Her2+++,My Hero!!
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