HonCode

Go Back   HER2 Support Group Forums > her2group
Register Gallery FAQ Members List Calendar Today's Posts

Reply
 
Thread Tools Display Modes
Old 09-17-2007, 10:01 AM   #1
PinkGirl
Senior Member
 
PinkGirl's Avatar
 
Join Date: Jul 2007
Location: Canada
Posts: 2,193
Question money

I have noticed that in some of the posts there is mention of insurance companies not paying for some treatments. Being a good Canadian, I have no idea what chemo treatments cost. Can anyone give me a ball park figure of what a year of herceptin costs? Anyone know what my chemo would have cost? I think I better give my little red and white health card a big kiss !!!
__________________
PinkGirl

Dx Aug/05 at age 51
2cm. Stage 2A, Grade 3
ER+/PR-
Her2 +++

Sept 7/05 Mastectomy
4 FAC, 4 Taxol, no radiation
1 year of Herceptin
Tamoxifen for approx. 4 months,
Arimidex for 5 years
Prophylactic mastectomy June 22/09



" I yam what I yam." - Popeye

My Photo Album
PinkGirl is offline   Reply With Quote
Old 09-17-2007, 10:21 AM   #2
Believe51
Senior Member
 
Believe51's Avatar
 
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
Talking Kiss It Girl

....and then sing "O Canada"..LOL!! We have had no health insurance since September 1 and it is not like he can get billed for infusions; as my hospital would be gracious enough to do that to help. My Sweet is on a regime of Tykerb/Xeloda, of course we are not going to get into how I am getting his chemo meds for him right now!!! Uggh!!!

So All Together Now: "O Canada"....giggle, giggle!!

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!!
Believe51 is offline   Reply With Quote
Old 09-17-2007, 10:32 AM   #3
hutchibk
Senior Member
 
hutchibk's Avatar
 
Join Date: Oct 2005
Posts: 3,519
Believe - I hope you are going through the Roche assistance program for Xeloda and GSK Commitment to Access for Tykerb!! That's how I get mine.
__________________
Brenda

NOV 2012 - 9 yr anniversary
JULY 2012 - 7 yr anniversary stage IV (of 50...)

Nov'03~ dX stage 2B
Dec'03~
Rt side mastectomy, Her2+, ER/PR+, 10 nodes out, one node positive
Jan'04~
Taxotere/Adria/Cytoxan x 6, NED, no Rads, Tamox. 1 year, Arimadex 3 mo., NED 14 mo.
Sept'05~
micro mets lungs/chest nodes/underarm node, Switched to Aromasin, T/C/H x 7, NED 6 months - Herceptin only
Aug'06~
micro mets chest nodes, & bone spot @ C3 neck, Added Taxol to Herceptin
Feb'07~ Genetic testing, BRCA 1&2 neg

Apr'07~
MRI - two 9mm brain mets & 5 punctates, new left chest met, & small increase of bone spot C3 neck, Stopped Aromasin
May'07~
Started Tykerb/Xeloda, no WBR for now
June'07~
MRI - stable brain mets, no new mets, 9mm spots less enhanced, CA15.3 down 45.5 to 9.3 in 10 wks, Ty/Xel working magic!
Aug'07~
MRI - brain mets shrunk half, NO NEW BRAIN METS!!, TMs stable @ 9.2
Oct'07~
PET/CT & MRI show NED
Apr'08~
scans still show NED in the head, small bone spot on right iliac crest (rear pelvic bone)
Sept'08~
MRI shows activity in brain mets, completed 5 fractions/5 consecutive days of IMRT to zap the pesky buggers
Oct'08~
dropped Xeloda, switched to tri-weekly Herceptin in combo with Tykerb, extend to tri-monthly Zometa infusion
Dec'08~
Brain MRI- 4 spots reduced to punctate size, large spot shrunk by 3mm, CT of torso clear/pelvis spot stable
June'09~
new 3-4mm left cerrebellar spot zapped with IMRT targeted rads
Sept'09~
new 6mm & 1 cm spots in pituitary/optic chiasm area. Rx= 25 days of 3D conformal fractionated targeted IMRT to the tumors.
Oct'09~
25 days of low dose 3D conformal fractionated targeted IMRT to the bone mets spot on rt. iliac crest that have been watching for 2 years. Added daily Aromasin back into treatment regimen.
Apr'10~ Brain MRI clear! But, see new small spot on adrenal gland. Change from Aromasin back to Tamoxifen.
June'10~ Tumor markers (CA15.3) dropped from 37 to 23 after one month on Tamoxifen. Continue to monitor adrenal gland spot. Remain on Tykerb/Herceptin/Tamoxifen.
Nov'10~ Radiate positive mediastinal node that was pressing on recurrent laryngeal nerve, causing paralyzed larynx and a funny voice.
Jan'11~ MRI shows possible activity or perhaps just scar tissue/necrotic increase on 3 previously treated brain spots and a pituitary spot. 5 days of IMRT on 4 spots.
Feb'11~ Enrolled in T-DM1 EAP in Denver, first treatment March 25, 2011.
Mar'11~ Finally started T-DM1 EAP in Denver at Rocky Mountain Cancer Center/Rose on Mar. 25... hallelujah.

"I would rather be anecdotally alive than statistically dead."
hutchibk is offline   Reply With Quote
Old 09-17-2007, 10:50 AM   #4
Believe51
Senior Member
 
Believe51's Avatar
 
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
Hey Brenda

As for the Tykerb, I did go through the 'Commitment to Access' program and things should be okay. The Xeloda I was able to get filled before 9/1 by the doctor rewriting the prescription a little different, we are set until the first week of November.

Question: He is out of Tykerb starting today. Is it alright to go a few days maybe a week without it?? (like we have a choice!!)

The disturbing thing about this was we refilled the prescription twice before they refused the next bulk drop!!

PS>Brenda, do you know the words to 'O Canada', because we could use you in our choir?? That is if you can put down the cheddar cheese and sesame crackers for a bit!! LOL...Love 'ya Brenda!!

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!!
Believe51 is offline   Reply With Quote
Old 09-17-2007, 11:16 AM   #5
hutchibk
Senior Member
 
hutchibk's Avatar
 
Join Date: Oct 2005
Posts: 3,519
I think they prefer that you don't go without... call Commitment to Access right now and tell them that he is out! They should be able to help you coordinate with the pharmacy to overnight it. (McKesson is the pharmacy who I receive it from, if it is yours as well, ask for Melinda there and she is very compassionate and will get it overnighted to you.)

I was instructed to call Commitment To Access about 10 days before my Rx runs out every month to be sure that I don't run out...

Hope this helps!

P.S. I always thought the words were 'No Canada'... or 'Blame Canada' - I guess I watch too much South Park, LOL.
__________________
Brenda

NOV 2012 - 9 yr anniversary
JULY 2012 - 7 yr anniversary stage IV (of 50...)

Nov'03~ dX stage 2B
Dec'03~
Rt side mastectomy, Her2+, ER/PR+, 10 nodes out, one node positive
Jan'04~
Taxotere/Adria/Cytoxan x 6, NED, no Rads, Tamox. 1 year, Arimadex 3 mo., NED 14 mo.
Sept'05~
micro mets lungs/chest nodes/underarm node, Switched to Aromasin, T/C/H x 7, NED 6 months - Herceptin only
Aug'06~
micro mets chest nodes, & bone spot @ C3 neck, Added Taxol to Herceptin
Feb'07~ Genetic testing, BRCA 1&2 neg

Apr'07~
MRI - two 9mm brain mets & 5 punctates, new left chest met, & small increase of bone spot C3 neck, Stopped Aromasin
May'07~
Started Tykerb/Xeloda, no WBR for now
June'07~
MRI - stable brain mets, no new mets, 9mm spots less enhanced, CA15.3 down 45.5 to 9.3 in 10 wks, Ty/Xel working magic!
Aug'07~
MRI - brain mets shrunk half, NO NEW BRAIN METS!!, TMs stable @ 9.2
Oct'07~
PET/CT & MRI show NED
Apr'08~
scans still show NED in the head, small bone spot on right iliac crest (rear pelvic bone)
Sept'08~
MRI shows activity in brain mets, completed 5 fractions/5 consecutive days of IMRT to zap the pesky buggers
Oct'08~
dropped Xeloda, switched to tri-weekly Herceptin in combo with Tykerb, extend to tri-monthly Zometa infusion
Dec'08~
Brain MRI- 4 spots reduced to punctate size, large spot shrunk by 3mm, CT of torso clear/pelvis spot stable
June'09~
new 3-4mm left cerrebellar spot zapped with IMRT targeted rads
Sept'09~
new 6mm & 1 cm spots in pituitary/optic chiasm area. Rx= 25 days of 3D conformal fractionated targeted IMRT to the tumors.
Oct'09~
25 days of low dose 3D conformal fractionated targeted IMRT to the bone mets spot on rt. iliac crest that have been watching for 2 years. Added daily Aromasin back into treatment regimen.
Apr'10~ Brain MRI clear! But, see new small spot on adrenal gland. Change from Aromasin back to Tamoxifen.
June'10~ Tumor markers (CA15.3) dropped from 37 to 23 after one month on Tamoxifen. Continue to monitor adrenal gland spot. Remain on Tykerb/Herceptin/Tamoxifen.
Nov'10~ Radiate positive mediastinal node that was pressing on recurrent laryngeal nerve, causing paralyzed larynx and a funny voice.
Jan'11~ MRI shows possible activity or perhaps just scar tissue/necrotic increase on 3 previously treated brain spots and a pituitary spot. 5 days of IMRT on 4 spots.
Feb'11~ Enrolled in T-DM1 EAP in Denver, first treatment March 25, 2011.
Mar'11~ Finally started T-DM1 EAP in Denver at Rocky Mountain Cancer Center/Rose on Mar. 25... hallelujah.

"I would rather be anecdotally alive than statistically dead."
hutchibk is offline   Reply With Quote
Old 09-17-2007, 11:28 AM   #6
PinkGirl
Senior Member
 
PinkGirl's Avatar
 
Join Date: Jul 2007
Location: Canada
Posts: 2,193
Post Brenda

I didn't get the part about No Canada, Blame Canada, and I don't know what South Park is .... probably because I am too busy paying my high, high taxes to cover our universal health care !!! Do you know how much herceptin and chemo drugs costs??? I really am curious - I have no idea what the price tag would be, or how much a mastectomy costs. I had back surgery in 1991 and only had to pay for the little TV in my room. I think Canadians should know how expensive health care is, and then we wouldn't abuse the system so much.(Canadians go to a doctor for absolutely every little ache, pain, cough, sneeze, itch ) We just go and never give a thought to how much it costs.
__________________
PinkGirl

Dx Aug/05 at age 51
2cm. Stage 2A, Grade 3
ER+/PR-
Her2 +++

Sept 7/05 Mastectomy
4 FAC, 4 Taxol, no radiation
1 year of Herceptin
Tamoxifen for approx. 4 months,
Arimidex for 5 years
Prophylactic mastectomy June 22/09



" I yam what I yam." - Popeye

My Photo Album
PinkGirl is offline   Reply With Quote
Old 09-17-2007, 12:03 PM   #7
Sheila
Senior Member
 
Sheila's Avatar
 
Join Date: Aug 2003
Location: Morris, IL
Posts: 3,507
Pink Girl
Love the name, love the Popeye saying!!!
I can tell you that Herceptin here in the USA varies by where you live...I know this because I filed a complaint with the Illinois Attorney General on the price my hospital/clinic was charging for Herseptin...3 times what others in this country were paying...after a big investigation, they did lower the price, and had to back pay the insurance and people for the charges that were TOO high....it is still more than alot of areas in the country...I can tell you that mine is $9,500 every 3 weeks, and $5200.00 every other week....just to let you know, my Avastin, Taxol and Herceptin every 2 weeks runs over $100,000 a month....and I don't pay a dime. I not only kiss my insurance card, I sleep with it!
__________________
"Be kinder than necessary, for everyone you meet
is fighting some kind of battle."



Hugs & Blessings
Sheila
Diagnosed at age 49.99999 2/21/2002 via Mammography (Calcifications)
Core Biopsy 2/22/02
L. Mastectomy 2/25/2002
Stage 1, 0.7cm IDC, Node Neg from 19 nodes Her2+++ ER PR Neg
6/2003 Reconstruction W/ Tissue Expander, Silicone Implant
9/2003 Stage IV with Mets to Supraclavicular nodes
9/2003 Began Herceptin every 3 weeks
3/2006 Xeloda 2500mg/Herceptin for recurrence to neck nodes
3/2007 Added back the Xeloda with Herceptin for continued mets to nodes
5/2007 Taken Off Xeloda, no longer working
6/14/07 Taxol/Herceptin/Avastin
3/26 - 5/28/08 Taxol Holiday Whopeeeeeeeee
5/29 2008 Back on Taxol w Herceptin q 2 weeks
4/2009 Progression on Taxol & Paralyzed L Vocal Cord from Nodes Pressing on Nerve
5/2009 Begin Rx with Navelbine/Herceptin
11/09 Progression on Navelbine
Fought for and started Tykerb/Herceptin...nodes are melting!!!!!
2/2010 Back to Avastin/Herceptin
5/2010 Switched to Metronomic Chemo with Herceptin...Cytoxan and Methotrexate
Pericardial Window Surgery to Drain Pericardial Effusion
7/2010 Back to walking a mile a day...YEAH!!!!
9/2010 Nodes are back with a vengence in neck
Qualified for TDM-1 EAP
10/6/10 Begin my miracle drug, TDM-1
Mixed response, shrinking internal nodes, progression skin mets after 3 treatments
12/6/10 Started Halaven (Eribulen) /Herceptin excellent results in 2 treatments
2/2011 I CELEBRATE my 9 YEAR MARK!!!!!!!!!!!!!
7/5/11 begin Gemzar /Herceptin for node progression
2/8/2012 Gemzar stopped, Continue Herceptin
2/20/2012 Begin Tomo Radiation to Neck Nodes
2/21/2012 I CELEBRATE 10 YEARS
5/12/2012 BeganTaxotere/ Herceptin is my next miracle for new node progression
6/28/12 Stopped Taxotere due to pregression, Started Perjeta/Herceptin
Sheila is offline   Reply With Quote
Old 09-17-2007, 12:12 PM   #8
Brenda_D
Senior Member
 
Join Date: Jan 2007
Posts: 368
My lumpectomy surgery was over $12,000, surgeon fees were over $1200.
My port placement cost over $6000, not including the doctor fees (another $1000). Then take into account pathologist, anesthesiologist, fees.
My chemo was over $1200 every 3 weeks (A/C), and Herceptin was $3745 the first time. Now it's $3100 plus $200 "other" and $115 doctor visit fees. That's every 3 weeks.
The rads were over $31,000.
I had a Pet/CT scan that cost $4700, a bone scan and a couple ct scans.
Add to that the cost of my medicine. Even the co-pay has totaled over $500 so far this year.
I am so glad I have insurance!
__________________
12/12/06- IDC Stage III, 4x A/C, 35 rads, Herceptin 1 year
Brenda_D is offline   Reply With Quote
Old 09-17-2007, 12:43 PM   #9
Andrea Barnett Budin
Senior Member
 
Andrea Barnett Budin's Avatar
 
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
Exclamation $$$$$$$$$$$$$$$$$$

I swear my husband just told someone recently that H was $15,000 ev 3 wks (inclding bld tests). I know Aranesp is up to $8,000 an injection. My doc, and I, believe Medicare is denying Aranesp to ca patients unless they are under 10 (new rule was under 11, which was under 12 to begin w/) because of the cost! Insur co are following the example. 13-15 is my normal, when I feel best. Yet I have lived in upper 11s w/Aranesp to boost when it drops to mid 11s and it last mnths. My red bld cells are boosted and so am I! Now I am 11.1 and feeling sluggish. I do take my nut/onc guru's supplements for energy and that helps big time. I'd be in bed otherwise. They did tell me last wk that if I spend more than 50% of my time in bed, I'm eligible. Isn't that a great criteria?

Then the nurse whispered that I could buy it in Canada and self-inject. That some do that. Well I can't imagine what that costs but I have no doubt it's not in my ballpark. And, thank goodness, I'm not on Taxotere, when my #s were in the toilet regularly. I could barely speak, my tongue weighed 50 lbs at least. I shuffled vs walked. Kept tripping on my own toes, while leaning on a wall, or Paul's arm. What of the chemo patients who are being ravaged????? SOMEBODY HAS TO FIX THIS.

I know about the scary studies re Aranesp and the like, but still, my onc and I feel it's really all about $$$. I've been on the drug since '98. Works for me. I think the fear tactics are mostly hype! And my onc concurs. Sad. So, it keeps the troops quiet. No one is fussing and protesting, too scared to demand tx for their flagging bld counts. Do we have to be crawling, or in need of a transfusion, dangerously low and prone to all kinds of infection and worse?????? Personally, I'm outraged.

I remember when the Procrit was $800 for the injection. That was astounding. I understand the need to stand up to the ?drug co's, the ?cancer center's, ridiculously rising charges, but meanwhile the ca patient in falling through the crack in the floor! At least I can keep on getting my Vit H w/o protest since '98. That is huge. And I treasure my insurance card, believe me. I don't leave the house w/o it! That + my driver's license, 2 credit cards and a $50 bill are my essentials. Oh, and some tissues. I have a YOU NEVER KNOW mentality, w/spares of everything. Wish I'd stockpiled Aranesp.

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...
Andrea Barnett Budin is offline   Reply With Quote
Old 09-17-2007, 01:15 PM   #10
hutchibk
Senior Member
 
hutchibk's Avatar
 
Join Date: Oct 2005
Posts: 3,519
Sorry to digress Pink -
* Tri-weekly charges from my cancer center to insurance for Herceptin alone (with the anti-emitics, streroids, benadryl, etc, etc) were apx $7000 usd.
*Taxol/Herceptin, tri-weekly charges were apx $11,000 usd.
*Taxol/Carbo/Herceptin tri-weekly charges were apx $17,000 usd.
*Tri-weekly labs and Dr. visit co-pays range between apx $200 - $500 usd.
*Aranesp is apx $4000 usd as charged by my ca cntr to ins.
*Neulasta is apx $6500 usd as charged by my ca cntr to ins.
*I think one month of Xeloda is apx $3500 usd - which is provided to me through an access program
*I think one month of Tykerb is apx $5000 usd - which is provided to me through an access program
*Day surgery to put in new port was apx $6000 usd. (then add anesth & surgeon fees)
*I can't remember what my mastectomy and reconstruction costs were 3 1/2 years ago, but I am guessing about $20,000 usd +.

Just to explain the 'Blame Canada' and SouthPark - it is an adult cartoon here in the US where the ficitonal characters (Stan, Cartman, Kyle, Kenny - all about 7 years old going on 40) got mad at the fictional Canadian govt for fictionally prosecuting their favorite fictional Canadian TV stars (for what I can't remember), Terrence and Phillip (who are flatulently profound and just totally goofy) - and wrote a song called 'Blame Canada'.... it is an absurd and often quite hilarious TV show... so no direct offense was intended from me to you or Canada. It was a direct reference to South Park.
__________________
Brenda

NOV 2012 - 9 yr anniversary
JULY 2012 - 7 yr anniversary stage IV (of 50...)

Nov'03~ dX stage 2B
Dec'03~
Rt side mastectomy, Her2+, ER/PR+, 10 nodes out, one node positive
Jan'04~
Taxotere/Adria/Cytoxan x 6, NED, no Rads, Tamox. 1 year, Arimadex 3 mo., NED 14 mo.
Sept'05~
micro mets lungs/chest nodes/underarm node, Switched to Aromasin, T/C/H x 7, NED 6 months - Herceptin only
Aug'06~
micro mets chest nodes, & bone spot @ C3 neck, Added Taxol to Herceptin
Feb'07~ Genetic testing, BRCA 1&2 neg

Apr'07~
MRI - two 9mm brain mets & 5 punctates, new left chest met, & small increase of bone spot C3 neck, Stopped Aromasin
May'07~
Started Tykerb/Xeloda, no WBR for now
June'07~
MRI - stable brain mets, no new mets, 9mm spots less enhanced, CA15.3 down 45.5 to 9.3 in 10 wks, Ty/Xel working magic!
Aug'07~
MRI - brain mets shrunk half, NO NEW BRAIN METS!!, TMs stable @ 9.2
Oct'07~
PET/CT & MRI show NED
Apr'08~
scans still show NED in the head, small bone spot on right iliac crest (rear pelvic bone)
Sept'08~
MRI shows activity in brain mets, completed 5 fractions/5 consecutive days of IMRT to zap the pesky buggers
Oct'08~
dropped Xeloda, switched to tri-weekly Herceptin in combo with Tykerb, extend to tri-monthly Zometa infusion
Dec'08~
Brain MRI- 4 spots reduced to punctate size, large spot shrunk by 3mm, CT of torso clear/pelvis spot stable
June'09~
new 3-4mm left cerrebellar spot zapped with IMRT targeted rads
Sept'09~
new 6mm & 1 cm spots in pituitary/optic chiasm area. Rx= 25 days of 3D conformal fractionated targeted IMRT to the tumors.
Oct'09~
25 days of low dose 3D conformal fractionated targeted IMRT to the bone mets spot on rt. iliac crest that have been watching for 2 years. Added daily Aromasin back into treatment regimen.
Apr'10~ Brain MRI clear! But, see new small spot on adrenal gland. Change from Aromasin back to Tamoxifen.
June'10~ Tumor markers (CA15.3) dropped from 37 to 23 after one month on Tamoxifen. Continue to monitor adrenal gland spot. Remain on Tykerb/Herceptin/Tamoxifen.
Nov'10~ Radiate positive mediastinal node that was pressing on recurrent laryngeal nerve, causing paralyzed larynx and a funny voice.
Jan'11~ MRI shows possible activity or perhaps just scar tissue/necrotic increase on 3 previously treated brain spots and a pituitary spot. 5 days of IMRT on 4 spots.
Feb'11~ Enrolled in T-DM1 EAP in Denver, first treatment March 25, 2011.
Mar'11~ Finally started T-DM1 EAP in Denver at Rocky Mountain Cancer Center/Rose on Mar. 25... hallelujah.

"I would rather be anecdotally alive than statistically dead."
hutchibk is offline   Reply With Quote
Old 09-17-2007, 02:14 PM   #11
PinkGirl
Senior Member
 
PinkGirl's Avatar
 
Join Date: Jul 2007
Location: Canada
Posts: 2,193
Smile holy sh#t...

That's a lot of money. When I started herceptin, I thought someone told me that the total cost of it was going to be $54,000 Cdn. That sounds low now that I've seen your estimates. I know the drug companies aren't as bad here as in the States - maybe that accounts for the difference.

Brenda - no offense taken - I just have never heard of South Park. Sounds a bit like the McKenzie Brothers - they drink beer, fart a lot, and say eh? Have you ever seen the Canadian bumper sticker: "When opportunity knocks, Canadians complain about the noise." We are a bit different up here !!!

Seriously, I can't imagine having to live with this nasty disease and also have to worry about paying for treatments. I really feel for those who do not have private insurance. I know if I ever need to have "pill" chemo, it is not covered the way the infusion kind is. I will have to buy the pills and submit the bills through my private drug/dental plan. I will get the money back, but I'll have to put out the money first (CREDIT CARD). If I didn't have a private drug/dental plan, there is a Foundation that would pay for the chemo pills.

Thanks for your replies. I think I will give my red and white card an extra kiss tonight.
__________________
PinkGirl

Dx Aug/05 at age 51
2cm. Stage 2A, Grade 3
ER+/PR-
Her2 +++

Sept 7/05 Mastectomy
4 FAC, 4 Taxol, no radiation
1 year of Herceptin
Tamoxifen for approx. 4 months,
Arimidex for 5 years
Prophylactic mastectomy June 22/09



" I yam what I yam." - Popeye

My Photo Album
PinkGirl is offline   Reply With Quote
Old 09-17-2007, 02:22 PM   #12
hutchibk
Senior Member
 
hutchibk's Avatar
 
Join Date: Oct 2005
Posts: 3,519
How much do you pay in taxes in Canada per year? Specifically to pay into the national health system?
__________________
Brenda

NOV 2012 - 9 yr anniversary
JULY 2012 - 7 yr anniversary stage IV (of 50...)

Nov'03~ dX stage 2B
Dec'03~
Rt side mastectomy, Her2+, ER/PR+, 10 nodes out, one node positive
Jan'04~
Taxotere/Adria/Cytoxan x 6, NED, no Rads, Tamox. 1 year, Arimadex 3 mo., NED 14 mo.
Sept'05~
micro mets lungs/chest nodes/underarm node, Switched to Aromasin, T/C/H x 7, NED 6 months - Herceptin only
Aug'06~
micro mets chest nodes, & bone spot @ C3 neck, Added Taxol to Herceptin
Feb'07~ Genetic testing, BRCA 1&2 neg

Apr'07~
MRI - two 9mm brain mets & 5 punctates, new left chest met, & small increase of bone spot C3 neck, Stopped Aromasin
May'07~
Started Tykerb/Xeloda, no WBR for now
June'07~
MRI - stable brain mets, no new mets, 9mm spots less enhanced, CA15.3 down 45.5 to 9.3 in 10 wks, Ty/Xel working magic!
Aug'07~
MRI - brain mets shrunk half, NO NEW BRAIN METS!!, TMs stable @ 9.2
Oct'07~
PET/CT & MRI show NED
Apr'08~
scans still show NED in the head, small bone spot on right iliac crest (rear pelvic bone)
Sept'08~
MRI shows activity in brain mets, completed 5 fractions/5 consecutive days of IMRT to zap the pesky buggers
Oct'08~
dropped Xeloda, switched to tri-weekly Herceptin in combo with Tykerb, extend to tri-monthly Zometa infusion
Dec'08~
Brain MRI- 4 spots reduced to punctate size, large spot shrunk by 3mm, CT of torso clear/pelvis spot stable
June'09~
new 3-4mm left cerrebellar spot zapped with IMRT targeted rads
Sept'09~
new 6mm & 1 cm spots in pituitary/optic chiasm area. Rx= 25 days of 3D conformal fractionated targeted IMRT to the tumors.
Oct'09~
25 days of low dose 3D conformal fractionated targeted IMRT to the bone mets spot on rt. iliac crest that have been watching for 2 years. Added daily Aromasin back into treatment regimen.
Apr'10~ Brain MRI clear! But, see new small spot on adrenal gland. Change from Aromasin back to Tamoxifen.
June'10~ Tumor markers (CA15.3) dropped from 37 to 23 after one month on Tamoxifen. Continue to monitor adrenal gland spot. Remain on Tykerb/Herceptin/Tamoxifen.
Nov'10~ Radiate positive mediastinal node that was pressing on recurrent laryngeal nerve, causing paralyzed larynx and a funny voice.
Jan'11~ MRI shows possible activity or perhaps just scar tissue/necrotic increase on 3 previously treated brain spots and a pituitary spot. 5 days of IMRT on 4 spots.
Feb'11~ Enrolled in T-DM1 EAP in Denver, first treatment March 25, 2011.
Mar'11~ Finally started T-DM1 EAP in Denver at Rocky Mountain Cancer Center/Rose on Mar. 25... hallelujah.

"I would rather be anecdotally alive than statistically dead."
hutchibk is offline   Reply With Quote
Old 09-17-2007, 03:21 PM   #13
sherri
Senior Member
 
Join Date: Sep 2005
Location: Vancouver, Canada
Posts: 329
Brenda,

In Canada richer people pay more tax: up to $30,000 income for a family of 4 (parent + 2 kids) pay a very little tax almost zero. up to 40,000 you pay 26% tax. then anything after $40,000 is about 33% and it goes up. Of course there are ways to lower your tax, like buying RRSP, investment etc.. But the the truth is that the people that have the opportunity to make more money pay more tax and take care of the unfortuate ones, but there is no child or anybody in Canada that is worried about paying bills for medical (hospital, drugs etc..)
In my case I would benefit more if we had private insurance, my tax rate with all those accounting tricks end up at about 40% of my income. But I like to tell you that I don't mind and sleep better at night, thinking all the children in this country get the best of the health care and no one has the right to send back a patient wandering on the street, even though that person is a drug addict.
Don't you think that is human nature to take care of the poor and unfortunate ? Maybe I'm naive?! ..... but I'm proud to think this way.
sherri is offline   Reply With Quote
Old 09-17-2007, 03:35 PM   #14
mrsd
Senior Member
 
mrsd's Avatar
 
Join Date: Feb 2007
Location: Nova Scotia, Canada
Posts: 40
I am just a lurker here usually but this thread is very interesting, and yes we do have excellent health care here in Canada but it is not without faults. For example each province uses it's health care money differently, I live in Nova Scotia and therefore my treatment options available under our government health care system may be different that say someone living in Alberta, for example our province does not cover the drug Avastin and this is currently a hot topic here right now. People who can afford the drug recieve the treatment and those who cannot afford the drug are having to drain savings and rely on community support to help pay for the treatments. Any form of other assistance from the cancer society and numerous others are limited by your income. So yes we do not pay for many many things and are not limited to who will treat us we are not without our faults............ sorry I don't mean to rant but it's just that I get upset by government determining treatment, I would rather be in the care of a doctor. But still very happy to be a Canadian in our strange system. And again sorry I didn't mean to rant but just wanted to point out the not so great points too, and I am amazed everyday when I read the post here how great everyone on this board is and how you all stick together and support each other, as you have been there and done that and you do know what we are going through.......thanks for telling it like it is.
__________________
Intial Dx Sept3,2002, age 39
Masct/ Sentinel Node Biopsy Sept 11,2002 node negative
ER/PR- Her2+++, grade 3
Started AC Chemo Nov 2002, 4 rds
2003 NED
May 2004 reconstuction, saline and later silicone implant
Aug 2006 Dx recurrence, lymph nodes chest/lungs/sternum
Dec 2006 Herceptin q three weeks
May 2007 bone mets to sternum
June 2007 aredia for bone mets
June 2007 radiation to sternum X 5
June 2008 slow progression of lung met, all other mets NED, continue Herceptin, Aredia, add Xeloda
July 08 Stopped Xeloda, severe side effects from the drug, but it did a fantastic job after only 12 days at least 50% reduction
Feb 09 Started Navelbine with herceptin, slight progression in lungs.
July 09 - Nov 09 had a Navelbine holiday...
Nov 09 back to Navelbine, Herception
Feb 10, lungs have improved but 4 small lesions on liver, started Taxol, Herceptin....
Taxol not the magic drug for me
Continuing Herceptin,Aredia,and adding Xeloda once again..reduced dose
mrsd is offline   Reply With Quote
Old 09-17-2007, 03:48 PM   #15
PinkGirl
Senior Member
 
PinkGirl's Avatar
 
Join Date: Jul 2007
Location: Canada
Posts: 2,193
Talking Sherri

I think that's the way we think because that's the way it has always been in Canada, in our lifetime. I agree with you - my husband and I are taxed in the 40% range and it doesn't bother us at all. Even before my dx., I didn't have a problem with it. I think it's because we can't believe that in a country as wealthy as the USA, there can be people not receiving health care because they can't pay for it. I don't think our system is perfect, but when I see some program on Oprah about parents who have a child needing a portable respirtor and they can't provide one, then I think "bring on the taxes". But there are some Americans who believe that our system is "Socialist". Once, an American tourist told me that Canadians were Communists!!!!!!!!!! There is an opinion that if you have a lot of money, you should be able to push yourself to the top of the line. As you probably know, there are wealthy Canadians who don't like being in our "universal " system; and I'm sure you know where they go when they are seriously ill -- The Mayo Clinic. Anyhow, I could go on and on about this. I am happy with our system, (with all it's flaws) and have always believed that you judge a nation by how it treats it's weakest citizen. I guess I'm a socialist. There's a provincial election coming up in Ontario -- go NDP!!!
__________________
PinkGirl

Dx Aug/05 at age 51
2cm. Stage 2A, Grade 3
ER+/PR-
Her2 +++

Sept 7/05 Mastectomy
4 FAC, 4 Taxol, no radiation
1 year of Herceptin
Tamoxifen for approx. 4 months,
Arimidex for 5 years
Prophylactic mastectomy June 22/09



" I yam what I yam." - Popeye

My Photo Album
PinkGirl is offline   Reply With Quote
Old 09-17-2007, 04:11 PM   #16
PinkGirl
Senior Member
 
PinkGirl's Avatar
 
Join Date: Jul 2007
Location: Canada
Posts: 2,193
Talking Brenda

We don't actually know how much of our taxes go to health care. We pay Federal taxes to the Government of Canada, and we pay Provincial taxes to our respective provinces. Because some of our provinces are not as wealthy as others, the Federal government gives money to the Provinces to help with health care budgets. Health care is a provincial responsibility, so there are differences between the care given. We also do not have the choices that you have in the States. We cannot just make an appt. with a specialist. Everything starts with a GP or your family doctor. They refer the patient to a specialist. To be cost effective, they are supposed to (but don't always) refer us to the closest specialist. When I was dx. I had my choice of 2 Cancer Centres, and I was assigned to an oncologist. I like my onc. but if I didn't, I would end up with another one at this centre, or start over at the other centre I could have gone to. My cancer centre is 5 hours away from where I live. I receive a travel grant of $265.00 every time I go there (I am there right now) I stay at a beautiful patient lodge, free of charge. It is like a 5 star motel. I am using their free internet right now. If I was so sick that I had to be flown here, the Canadian Cancer Society would fly me here, but I would have to give them my $265.00 grant. If I am flown from one hospital to another hospital, that is covered by our health insurance. I was dx. in August/05, mastectomy Sept/05 and started chemo Oct./05. So.......what can I say...we have excellent health care, but we don't have the choices you have. I'm sure you can't imagine being told who your oncologist is going to be !!! I could go on and on about this..........Gotta go to bed... I have my scans tomorrow.
__________________
PinkGirl

Dx Aug/05 at age 51
2cm. Stage 2A, Grade 3
ER+/PR-
Her2 +++

Sept 7/05 Mastectomy
4 FAC, 4 Taxol, no radiation
1 year of Herceptin
Tamoxifen for approx. 4 months,
Arimidex for 5 years
Prophylactic mastectomy June 22/09



" I yam what I yam." - Popeye

My Photo Album
PinkGirl is offline   Reply With Quote
Old 09-17-2007, 04:27 PM   #17
sherri
Senior Member
 
Join Date: Sep 2005
Location: Vancouver, Canada
Posts: 329
NDP for sure!
sherri is offline   Reply With Quote
Old 09-17-2007, 04:38 PM   #18
Andrea Barnett Budin
Senior Member
 
Andrea Barnett Budin's Avatar
 
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
$$$$$$ Correction.

$$$$$$$$$$ CORRECTION. For H the cancer center BILLS $8,000 ev 3 wks. They get around $2000. It's a game. They keep billing more and getting more, but the #s don't actually coincide. And then, it's back to the Aranesp issue, which I won't repeat but is above in my post. Apparently not an issue in Canada.

U.S. NEEDS HEALTH CARE REFORM. We all know that. Insurance co's are making medical decisions, even contrary to our docs recommendations. Clerks behind a desk can override him/her, just to save $$$$$. And Medicare leads the way, which is not a good thing to say the least. And yes, you judge a society by how they care for he less fortunate among them. We're in a quagmire of a mess. But I did get to choose 5 oncs on my own, choose my surgeons, etc. And I can purchase Aranesp on the black market, from Canada and self-inject. IF I had a whole bunch of $$$ to afford such a luxury. Our system is badly broken and we all know it.

My neice is uninsured b/c she comes from divorced parents and he won't pay and she can't pay, so my neice hasn't been to a GYN ever, etc... New administration has to fix this + solve Iraq... Meanwhile...

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...
Andrea Barnett Budin is offline   Reply With Quote
Old 09-17-2007, 05:08 PM   #19
dhealey
Senior Member
 
Join Date: Jun 2007
Location: moved to Lancaster, Pa in June, 2010
Posts: 576
It is interesting the different prices for some of the same treatment. My first mastectomy was $10,000 that inculded a night's stay in the hospital and surgeon, pathology fees. My adramycin/cytoxin was $8,500 every other week, lunasta shot $6000 every two weeks, taxol/herceptin was $8,000 everyother week, anarasep $3000 every three weeks and now just on herceptin runs $4,800 every three weeks not including labs. My second mastecomy ran about $7,000 and I did not stay the night this time. Echo run $2,000 every three months and the cardiologist charges $500 to read it. It makes me dizzy thinking of all that money! About 2 months ago I added up my charges to date and I hit over $100,000 and I have only been in treatment 8 months. Mind boggling!!!!
__________________
Debbie in North Carolina
Diag 10/2006-high grade invasive ductal carcinoma- mastectomy L breast
2.5 cm tumor ER/PR pos-Her2+++
4 rounds A/C, 4 rounds Taxol
Herceptin every 3 weeks until Jan. 2008
6/18/07 prophylatic mastectomy R breast
8/2007 started aromasin/stopped arimidex (side effects)
12/07 stopped aromasin due to side effects (now what?)
Finished herceptin 1/8/08
started tamoxifen for 2 years then will switch to femera
allergic to tamoxifen started femera 4/2008
June 20, 2008 portacath removed
Learnig to live life to the fullest!
Stopped Femera due to side effects
July 28, 2008 start trial for breast cancer vaccine
dhealey is offline   Reply With Quote
Old 09-17-2007, 05:36 PM   #20
PinkGirl
Senior Member
 
PinkGirl's Avatar
 
Join Date: Jul 2007
Location: Canada
Posts: 2,193
Talking Oh Canada

Andi - like your niece, I also have never been to a GYN !!! I have my internals and pap smears done by my family doctor. If she thinks there is a problem, then I get referred to a specialist ( a gyno ). I have normal paps, normal internals, no symptoms of anything, so no GYN. Now, if I insisted, she would refer me to one, because of the BC.
__________________
PinkGirl

Dx Aug/05 at age 51
2cm. Stage 2A, Grade 3
ER+/PR-
Her2 +++

Sept 7/05 Mastectomy
4 FAC, 4 Taxol, no radiation
1 year of Herceptin
Tamoxifen for approx. 4 months,
Arimidex for 5 years
Prophylactic mastectomy June 22/09



" I yam what I yam." - Popeye

My Photo Album
PinkGirl is offline   Reply With Quote
Reply


Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off

Forum Jump


All times are GMT -7. The time now is 11:31 AM.


Powered by vBulletin® Version 3.8.7
Copyright ©2000 - 2024, vBulletin Solutions, Inc.
Copyright HER2 Support Group 2007 - 2021
free webpage hit counter