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Old 11-14-2007, 07:28 PM   #1
Andrea Barnett Budin
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Join Date: Oct 2005
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 Just Me...

It's just me again. Same message, but different... I do not believe the anti d's cause ca. I believe the toll of the chemical alteration in your bodymind causes T cells to plummet (actually proven in many studies -- linked w/stress, distress, pp out of work, loss of loved one, etc.). This leaves your immune system not in good fighting position and open/prone to infection and malfunction/dysfunction. Ca is out of control cells run amok, w/no NKs (natural killers) around to hold them off. Joanne, please read Leslie's fab links. Read my post in this thread re this. Step back. Become The Witness. The Observer. Change your perspective a bit, from a distance. It is an astounding realization that can EMPOWER you and change your life forever...

I haven't adequate words to say how sorry I am that you lost a daughter. As I first read your words something clutched at my heart and choked it. I gasped. How utterly devastating such an experience has to be. Can you ever recover? Surely Zoloft and the like will assist you in getting your footing and embracing Life with gusto, as I have no doubt, your daughter wishes for you. You will put your arms around her again. For now, live for her, in memory of her, as a tribute to her. That is the best you can do. With much loving, healing energy sent from me to you, with my deepest respect for you and all you have had to endure...
Andi

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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 11-14-2007, 08:32 PM   #2
Joanne S
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Location: Detroit Metropolitan Area, Michigan
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Smile Hey Just Me Again...

Bless you Andi!

Oh ---I hate it so much when I type a long thought out response and somehow manage to lose it.

Here's a short version cuz I tired and frustrated now.

Thanks for responding to my post about depression and anti-ds, and for your suggested reading. I will read them. What enthusiasm you have!

I can relate to your dosage amount. When I started taking Zoloft many years ago, I could only handle 1/8 of the smallest dosage. During some of life's chuck holes, my brother's leg amputation....I've had to up it to 250 mg. I've been mostly on 100mgs for the duration.

I handled my initial dx of BC very well and had a very positive attitude during the first 9 months. Several of my doctors recommended uping my dosage to 200 mg again to aid with my chest pain and depression from the frustration of dealing with the pain. (Doing better now with the addition of Neurotin and physical therapy.)

Thank you so much for your very kind,compasionate and supporting words.

Wishing you continued improvement and wellness,
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Aug06...Dx Age 50, IDC Left Breast, 6+/16 lymph nodes, Stg 3, ER+/PR+/HER2+
Sep06-Jan07...Mediport. Chemo: AC x 4, T x 4
Dec06-Nov07...Herceptin
Feb12,2007...Surg MRM Left & SM Right, reconstruct w/expanders
Mar07-Jun07...Saline Exp
Jun07...Start Tamoxifen
Jun07-Aug07...Rad x 25
Jun07-Oct07...Persistent fevers-unknown origin
Jun07-Nov07...PT for Severe PMPS & Capsular Contracture
Nov07...Surg Capsulectomy, Gel Implants, PMPS pain gone instantly.
Feb08...NED 1st CANCERVERSARY!!!!!
Feb08...2 months post surgery Caps Cont again :(
Mar08...Stop Tamoxifen. Start Arimidex.
Apr08...Sudden high fever, Hosp ICU 10 days, staph infect, emerg surg, implants removed. Outpt IVantibiotics Daily x 6 weeks
Feb11...NED 5th CANCERVERSARY!!!!!
Feb12...NED 6th CANCERVERSARY!!!!!
Aug12...Spotting. Surg=D&C
Sep12...STAGE IV = RARE BC METS TO UTERUS ILC ER+/PR+/HER2-Negative) (Different BC than originally diagnosed = IDC ER+/PR+/HER2+).
Sep12...Stop Arimidex. Start Afinitor & Aromasin.
Jan13...MRI = no progression no reduction
Apr13...Progression. Stop Afinitor & Aromasin.
Apr13...Start Chemo: Taxol & Carboplatin.
Nov13...Scans & Pelvic 95+% Reduction. Nueropathy>Stop chemo start Fareston.
Jan14...PET scan = no progression stable.
May14...Pelvic > Bleeding & cramps. TMs up.
May14...PET scan = uterine progression :(
May14...Stop Fareston. Start Chemo: Xeloda.



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