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07-27-2007, 01:15 PM
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#1
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Senior Member
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
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One Little Pill
I was never a pill taker, but bc changed that. My oncs said -- You know you don't get a medal for suffering. There is no reason for you to be in pain. They do not give out awards for such things. Take the pain pill. BEFORE it gets bad, before it gets out of hand. Be good to yourself.
Before a brain MRI, I confess, I take an Ativan. In fact, my onc told me to take 1 the night before as well, to get a good night's sleep and not worry. He's the one, in '98, who pushed me to do Taxotere, the most highly aggressive weapon at the time, to fight my highly aggressive ca. Tailor-made. A mean nasty drug that did the job, so I love it.
In the MRI machine, I doze. I bring my Andreas Bocelli Romanza CD and they give me headphones and I drift into reverie. I have my husband drive! This last time, I woke and it wasn't quite done. I decided to be brave (super serene from my one little Ativan) and take a peak. It was WAY BIGGER in there than I imagined. I thought the machine would be inches from my nose. It was roomy. Or so it felt at the time. So, now, I don't think I'll need the Ativan next time. I am a bit claustrophobic, but this is not what I'd envisioned. THE REALITY IS RARELY AS BAD AS WE CONJURE UP FOR DAYS, EVEN WEEKS BEFORE. Have you noticed that?
As for INSCANITY -- I still get it. I request a same day report, scheduling myself for the first appointment of the day, to allow TIME, for the report to be emailed to my doc who calls me. I call the doc the moment I get home and remind his nurse that I will be sitting by the phone, with my husband, awaiting their call. After all these years, we sit on pins and needles waiting to hear -- STABLE. We bought some more time! Yeah! Celebration. In '98/'99 we'd get exact measurements of each and every multiple tumor in my liver and compare sizes from the last report. Paul would take the square root which clarified and seemed to magnify what didn't at first appear to be much progress. We (the Taxotere, Herceptin, me and Paul and my oncs) knocked every damn cell out. I DID get in the way some, but I am glad I took the most difficult path. It was just what I needed. Facing lousy odds, I just did what I had to and prayed and focused my ENERGY and thoughts, meditated, used guided imagery and took (and take) heaps of supplements to keep my immune system in fighting spirit and all systems cooperating in HEALING.
This is what I wish for all my Sisters. Don't just ask for a miracle -- insist on it -- call it to you, with the power of your consciously chosen mental dialogue that plays out in your head all day! Signal the Universe with the purest most passionate ENERGY you can muster, and it will sense your vibrations going out and match them IN KIND!
Sending you loving, healing energy and prayers all... 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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07-27-2007, 01:55 PM
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#2
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Senior Member
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: 3,000
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That is soooooooo right!!!
Amen Andrea, that is what I am doing right now.
Waiting For A Miracle.....'and commanding one soon'>>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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07-27-2007, 02:00 PM
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#3
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Guest
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Jean--I had an MRI just a few weeks ago, worried about brain mets. I didn't have headache, however, but dizziness and nausea. The results were negative and I was so relieved. I put off telling my oncologist or anyone of my symptoms for a while, as I was afraid the test would come back positive, but finally told my oncologist and he ordered the MRI. The weeks of anxiety I went through thinking it was mets was far worse than the anxiety of waiting for test result.
I found the MRI very easy to do, except the contrast part. Because I was in the machine when they had to access vein, I couldn't direct them and at first they went for a vein that never works, with lots of pain and bruising. So if you decide to get one, make sure they understand before they start which veins are acceptable and which aren't. Other than that it was a very easy test compared to some others I've had.
I suspect most of us get headaches for a few days or so, for whatever reason, and in the past we would have ignored them. I did tell my oncologist that I was embarrassed he'd think I was a hypochrondriac. I liked his response: "Before cancer you would have been; after cancer it's not possible. Always be concerned about symptoms."
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07-27-2007, 02:21 PM
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#4
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Senior Member
Join Date: Jan 2007
Location: Massachusetts
Posts: 82
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Thanks!
Thanks to all of you for your wisdom and support! I went to the onc NP today. She ordered an MRI which I'll be having on Sunday morning. (I had my first brain MRI in January before starting chemo.) I'm going to take Ativan beforehand. The NP said that I'll get the results by Monday evening. I'm hoping for a sinus problem!
I really appreciate everyone's input!
Jean C.
__________________
IDC Stage IIIA
Diagnosed Nov 2006 (routine mammogram), age 51
Lumpectomy, lymph node dissection Dec 2006
3 cm tumor, 8 cancerous lymph nodes
Grade 3, ER/PR -, HER-2/neu +++ (by FISH, average 20 copies per cell)
A/C x 4, Taxol x 12, Herceptin x 47 weeks
35 radiation treatments
Completed treatment on April 3, 2008
Chest port removed October 2009
11 years since diagnosis NED
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07-27-2007, 02:31 PM
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#5
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Senior Member
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
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Don't Pop A Pill And Drive!
Jean,
Did I say that when I take an Ativan (other than before going to sleep) -- I make sure someone else drives! You can't predict how you will react, but I wouldn't take a Xanax or painkiller and DRIVE!
Lots of luck to you. Hoping for a bout w/the sinuses. Or stress. Or anything other than mets. Will say a prayer for you, and for Marie's husband, and for Adriana and for Brenda and all Sisters in need of one... LOVE, 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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