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Old 01-27-2008, 10:25 PM   #1
harrie
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sicko by MM

Did anyone see Sicko, a documentary by Michael Moore? It is about health insurance. I thought it was very interesting. Any comments?
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*** MARYANNE *** aka HARRIECANARIE

1993: right side DCIS, lumpectomy, rads
1999: left side DCIS, lumpectomy, rads, tamoxifen

2006:
BRCA 2 positive
Stage I, invasive DCIS (6mm x 5mm)
Grade: intermediate
sentinal node biopsy: neg
HER2/neu amplified 4.7
ER+/PR+
TOPO II neg
Oncotype dx 20
Bilat mastectomy with DIEP flap reconstruction
oophorectomy

2007:
6 cycles TCH (taxotere, carboplatin, herceptin)
finished 1 yr herceptin 05/07
Arimidex, stopped after almost 1 yr
Femara
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Old 01-28-2008, 01:24 AM   #2
RhondaH
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Smile Maryanne...

I TOO saw it and I think there is a lot of truth to it (PART of my belief comes from the fact that I USED to work for Travelers Insurance in their "Specialty claims" department...I.E. we paid/denied STRICTLY long term nursing care, chiropractic and podiatry claims and there was a registered RN I worked with to "save" the company money...deny claims...I worked there from 1987 to 1990, so nothing recent when I got a "conscience"). Take care and God bless.

Rhonda
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Rhonda

Dx 2/1/05, Stage 1, 0 nodes, Grade 3, ER/PR-, HER2+ (3.16 Fish)
2/7/05, Partial Mastectomy
5/18/05 Finished 6 rounds of dose dense TEC (Taxotere, Epirubicin and Cytoxan)
8/1/05 Finished 33 rads
8/18/05 Started Herceptin, every 3 weeks for a year (last one 8/10/06)

2/1/13...8 year Cancerversary and I am "perfect" (at least where cancer is concerned;)


" And in the end, it's not the years in your life that count. It's the life in your years."- Abraham Lincoln
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Old 01-28-2008, 06:56 AM   #3
CPA
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If you really think that the "free" healthcare in Cuba, that he claims is so wonderful, is better than what you get here in the U.S. then I have some prime Miami condominiums that you might be interested in buying...

Our system is not perfect, but I have seen enough & even read enough on these boards to know that no other system is perfect either.

My general impression of MM is that he is an opportunistic leach who cares less about the truth than in making money for himself and embarrassing those who do not hold his same narrow minded views.
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Husband to Jill
Diagnosed 10/05, age 39
R Mast 11/05
Stage II N0
Her2+ er/pr+
Revision Mast due to positive margins 12/05
TCH Chemo started 1/06
Finished TC 4/06
Tamoxifen
Finished H 12/29/06
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Old 01-28-2008, 07:10 AM   #4
cafe1084
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I saw sicko a few months back and it was eye-opening to say the least. It made me want to move to another country to live, but there are always downsides to anything that seems to be better....you know what they say about the grass being greener on the other side. I work with a nurse who worked for an HMO for years before his career change. That's basically why he changed careers. He said he found it difficult to sleep at night knowing he may have held partial responsibility in the deaths of people who were being denied needed treatments and services, just to save on the bottom line. I wish our system worked better for us, but it's the only system we have at this time. I have good, not exceptional insurance, but I cannot imagine what could've happened to me during this whole cancer fight without it. Just 5 short years ago, I had no health insurance. I didn't think I needed it, so I never opted for it at work. I make too much money to qualify for medicaid, unless I lose everything I've worked so hard for, yet the insurance premiums are breaking the bank. I don't have an answer and it stinks that we are forced to play the cards we are dealt until someone overhauls the system to work for the people who are making them rich and greedy
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Old 01-28-2008, 08:32 AM   #5
Karen W
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I lived in Australia for a while and didn't really like the health care system there (I loved the county and the people though). I know that our system isn't perfect but I do not want National Health Care here.

Karen
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Old 01-29-2008, 12:03 PM   #6
doh2pa
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I saw Sicko just last week. My husband and I are both in the health care field and realize this system is not perfect. But Mr Moore's view was very one sided. If you talk to people in Canada and Great Britain they do not have the same high opinion of the quality of the care they receive there. Some of what he says is certainly true, and we could use some improvement, but don't believe that the grass is necessarily greener.
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Donna
Diagnosed 2/04 - Invasive ductal - no clean margins
node negative - er+pr+, her2++
Mastectomy 4/04 - 4 rounds AC
9/05 - mets to liver treated with carbo/ixabipelone/herceptin
3/06 - complete remission
9/06 - new liver mets, starting Taxotere/Herceptin
1/07 -Liver mets stable, staying on Herceptin
5/07 - Liver, lung progression - starting T/X
12/07 - Liver, lung progression - starting weekly Navilbene/Herceptin
4/08 - Liver progression - started Abraxane, Carbo, Tykerb and Herceptin
7/08 - Liver Progression - started Gemzar, Avastin and Tykerb
10/08 - Liver progression - starting Doxil
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Old 01-29-2008, 11:54 PM   #7
harrie
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Interesting comments....thank you.
Maryanne
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*** MARYANNE *** aka HARRIECANARIE

1993: right side DCIS, lumpectomy, rads
1999: left side DCIS, lumpectomy, rads, tamoxifen

2006:
BRCA 2 positive
Stage I, invasive DCIS (6mm x 5mm)
Grade: intermediate
sentinal node biopsy: neg
HER2/neu amplified 4.7
ER+/PR+
TOPO II neg
Oncotype dx 20
Bilat mastectomy with DIEP flap reconstruction
oophorectomy

2007:
6 cycles TCH (taxotere, carboplatin, herceptin)
finished 1 yr herceptin 05/07
Arimidex, stopped after almost 1 yr
Femara
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Old 01-30-2008, 06:34 AM   #8
kcherub
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Hi, Harrie (MA)!

I saw SICKO a few months ago, and I found it thought-provoking and very interesting. I have always believed that our health care system could use improvement, but what this is--who knows?!? Just as there are those who love their countries universal health care system, there are those that do not. It is the same way here, but...

I am lucky that I have great insurance, and that I haven't had any "real" problems getting the treatment I wanted/needed (so far). I found myself getting really angry when hearing the stories of those who did not. The wife who requested a bone marrow transplant (wasn't it that?) for her husband just burned my butt. How long does something have to be around for an insurance company to not be able to label it "experimental"? Ugh. The medication issue and costs? OMG--how is that possible?

I know a lot of people look at MM as a political thing (demo. vs. repub.), but I look at him as just another entertainer with a bit of investigational journalism thrown in. Yes, he is over the top, but I don't see myself making any major lifestyle changes due to his films. It is just like everything else--no one is going to agree with everyone else's opinions all of the time.

Great topic--gives us something else to chat about.

Much love,
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Krista
Diagnosed 3/29/2007 @ age 34
Stage 1, Node Neg. (SNB), Grade 2, 1.4 cm. IDC
ER/PR 90%+ HER2 +
6 TCH started 5/25/2007, ended after #5 due to steroid "reactions" and neuropathy in feet and hands
BUT--#6 CH w/o Taxotere
Begin Herceptin alone 9/28/2007
30 rads completed 12/19/2007
Finish Herceptin 5/9/2008
Stopped Tamoxifen early--HATED it.
Married 17 years
13-year old son
3 embies on ice (from 1999)
GA, USA

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Old 01-30-2008, 03:12 PM   #9
Vanessa
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I have a friend from Canada and he told me the Canadians would revolt if their healthcare system was taken away.
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Old 01-30-2008, 03:21 PM   #10
PinkGirl
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Yes Vanessa, your friend is correct.
We would revolt.
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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

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Old 01-30-2008, 05:18 PM   #11
caya
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Yes Vanessa - I'm with Pink, we would revolt.

This topic has been discussed before, and as a Canadian who has lived here all my life, I will restate my opinion on the Canadian Health Care System - it is not perfect, I am the first to admit that. However, it does provide equal access to all citizens, from everyday checkups at your GP, to getting second opinions with any doctor YOU choose, not just who is in your "network",to covering Herceptin treatments for us Her2neu+ BC patients. No fights with insurance companies, no co-pays etc. No insurance company has ever dictated to me what tests/scans I get - my oncologist, breast surgeon and I make those decisions.

Yes, we pay high taxes - but I feel it is well worth it. The stress of dealing with my DH's brain aneurysm and my BC dx within 9 months of each other was devastating enough, I cannot imagine having to worry about paying for treatment, or not seeing the drs. we personally wanted to. We got topnotch treatment in a timely manner at world class hospitals. We also never have to worry that if you lose your job, you lose your health care insurance - another stressful situation.

Yes, you will hear about how some surgeries are delayed etc. up here in Canada due to long waiting lists - but these are the few exceptions to the rule. We can't have everything - immediate surgeries, world class doctors/equipment etc. and equal access for all without something giving in occasionally. And most people realize that and this is being looked at by our government. But I'd rather have it this way - I did not have to fill out one form or answer to anybody during my entire course of treatment.

After my husband's brain surgery, he spent 6 nights in a neuro ICU, and when he came home a nurse/social worker was sent in every week to monitor his progress and did cognitive testing with him. After my mastectomy a nurse came every day to change my dressing for about 3 weeks and help me with my drains. This was all covered by the health care system. I had meetings with nutritionists, psychologists, social workers etc. - all covered.

I can only speak of my own experiences, again I fully acknowledge it is not a perfect system, but I think most Canadians are happy with the care they get.

all the best
caya
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ER90%+/PR 50%+/HER 2+
1.7 cm and 1.0 cm.
Stage 1, grade 2, Node Negative (16 nodes tested)
MRM Dec.18/06
3 x FEC, 3 x Taxotere
Herceptin - every 3 weeks for a year, finished May 8/08

Tamoxifen - 2 1/2 years
Femara - Jan. 1, 2010 - July 18, 2012
BRCA1/BRCA2 Negative
Dignosed 10/16/06, age 48 , premenopausal
Mild lymphedema diagnosed June 2009 - breast surgeon and lymph. therapist think it's completely reversible - hope so.
Reclast infusion January 2012
Oopherectomy October 2013
15 Years NED!!
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Old 01-30-2008, 08:00 PM   #12
mke
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Well yes I'm happy in Canada and my care and that of my family has always been exemplary. There are waiting lists for elective procedures like joint replacements and cataract surgery. ER waiting times can be awful, except for those who really need to be in the ER. In remote areas access to medical care is difficult. The lobbyists for the status quo in the US are going to stress those facts.

No system is perfect, I know that with endless funds I could get faster care in the US. I am not sure I would get better care.

In the late 80's I was a second level manager in a community hospital with around 400 beds, the usual mixture of chronic, medical, surgical, about 20 mental health beds, lots of maternity traffic. There was purchasing dept with around 3 or 4 people. There were about 5 secretaries in total, one of whom did billing part time.
One night I watched a documentary about a hospital in Oregon, same size more or less, same mix more or less. There was a whole separate building full of people who did nothing but billing.

And that is exactly why US citizens pay 60% more for worse outcomes, why by any accepted measure of public health they are way down on the list. You aren't paying your health care providers - you pay your insurers.
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Mary in Toronto

1998 left side ER/PR+, node-, lumpectomy and rads
2005 right side ER/PR-/HER2+, nodes+, neoadjuvant AC, taxol, lumpectomy, rads, 12 months herceptin
2008 back to the left, ER/PR+/HER2-, node-, bilateral mast.
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Old 01-31-2008, 12:02 AM   #13
harrie
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For the Canadians....

Would you happen to know if your insurance would cover the Oncotype Dx or pay significanlty for post-mastectomy reconstruction? I was extremely disappointed with my private ins co in HI. Medicare would have done better and I have a private dual PPO. I have written my appeals.
Harrie
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*** MARYANNE *** aka HARRIECANARIE

1993: right side DCIS, lumpectomy, rads
1999: left side DCIS, lumpectomy, rads, tamoxifen

2006:
BRCA 2 positive
Stage I, invasive DCIS (6mm x 5mm)
Grade: intermediate
sentinal node biopsy: neg
HER2/neu amplified 4.7
ER+/PR+
TOPO II neg
Oncotype dx 20
Bilat mastectomy with DIEP flap reconstruction
oophorectomy

2007:
6 cycles TCH (taxotere, carboplatin, herceptin)
finished 1 yr herceptin 05/07
Arimidex, stopped after almost 1 yr
Femara
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Old 01-31-2008, 06:35 AM   #14
CPA
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http://her2support.org/vbulletin/showthread.php?t=32433

BBC report posted by Lani. I think it applies to this discussion.
__________________
Husband to Jill
Diagnosed 10/05, age 39
R Mast 11/05
Stage II N0
Her2+ er/pr+
Revision Mast due to positive margins 12/05
TCH Chemo started 1/06
Finished TC 4/06
Tamoxifen
Finished H 12/29/06
Currently NED
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Old 01-31-2008, 07:27 AM   #15
caya
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Harrie,

I can only speak for the Ontario system, but I know that post-mastectomy reconstruction surgery is fully covered. I'm not sure about the Oncotype DX test - that one may not be covered.

all the best
caya
__________________
ER90%+/PR 50%+/HER 2+
1.7 cm and 1.0 cm.
Stage 1, grade 2, Node Negative (16 nodes tested)
MRM Dec.18/06
3 x FEC, 3 x Taxotere
Herceptin - every 3 weeks for a year, finished May 8/08

Tamoxifen - 2 1/2 years
Femara - Jan. 1, 2010 - July 18, 2012
BRCA1/BRCA2 Negative
Dignosed 10/16/06, age 48 , premenopausal
Mild lymphedema diagnosed June 2009 - breast surgeon and lymph. therapist think it's completely reversible - hope so.
Reclast infusion January 2012
Oopherectomy October 2013
15 Years NED!!
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Old 01-31-2008, 07:54 AM   #16
mke
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Reconstruction would be covered in Ontario. I have been clear from the onset that I have no interest in it. I don't know about the oncotype.
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Mary in Toronto

1998 left side ER/PR+, node-, lumpectomy and rads
2005 right side ER/PR-/HER2+, nodes+, neoadjuvant AC, taxol, lumpectomy, rads, 12 months herceptin
2008 back to the left, ER/PR+/HER2-, node-, bilateral mast.
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Old 01-31-2008, 09:39 AM   #17
sarah
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I live in France and I LOVE the universal health care here and the French would have a revolution if it was taken away. It's also extremely high quality. I'm so glad I'm here.
First time around I was in the US; the recurrence happened in France. I'll take France over the so called "great health insurance" I had in the US. Also the US government pays twice as much per person as countries with universal pay, so who's really paying??? the taxpayer and then there are so many without any insurance. Is that fair? I can chose my doctors. I discuss my treatment with my doctors. In a USA PPO or HMO, you can't chose any doctor, only from a list.
My father was a doctor and he was for universal health care. He worked 3 mornings a week free in a clinic because he believed everyone should get good medical care and that good medical care for everyone was safer because that way no potentially dangerous infection - such as untreatable tuberculosis could get out of hand. He'd been alive (a child) when the influenza epidemic killed millions.
sarah
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Old 02-01-2008, 09:50 PM   #18
hutchibk
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http://www.cbsnews.com/stories/2005/...tml?cmp=EM8705
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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."
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Old 02-02-2008, 08:11 AM   #19
caya
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Brenda,

With all due repect,that article you posted is nearly 3 years old. If you search through the internet you will find articles like this, as Mke said, the lobbyists in the US against universal health care will stress things like this. As I said previously, I fully admit that the Canadian universal health care system is not perfect. And BTW, in this article you cited, the WHO in 2000 ranked Canada 30th in health care, and the US 37th, not exactly positions either country should be proud of.

Unfortunately I am not as tech savvy as you, so I cannot bring up a link directly, but just a few months ago it was front page news across all the Canadian papers - a woman from Seattle (I think) was advertising for a Canadian husband because she had no health insurance and could not get it in the States - She knew if she married a Canadian, she would be covered.

I personally know of a Her2 BC patient in Wisconsin whose oncologist has been trying to get her a PET scan for weeks - fighting with her insurance company. Another woman I know in California - her husband has just been diagnosed with prostrate cancer and their insurance will not cover the latest robotic surgery. Many Americans think "the government" will dictate what their care will be, if they have universal health care. Well, to me, it seems like in the States, the insurance companies have the final word - if you have coverage at all. And you have to stay within your HMO or Network- here I can go to any doctor/hospital I want to. Yes, I need a referral to see a specialist from my GP, but that is just a formality.

And if universal health care is the big bad beast, why are both Hilary Clinton and Barak Obama making this such a big election issue in their campaigns? (Sorry I don't know much about the Republican candidates). Ask the 47 million Americans who do not have any insurance what they would prefer. Ask people who are stuck in jobs they hate, but are afraid to leave because they would lose their health insurance.

You can bring up articles showing the "failures" of the Canadian system all you want - but I can tell you that, while not perfect, and I stress that, most Canadians are very happy with our system. We have very good care, in general, for EVERYONE. No one is losing their house to pay for medical treatments in Canada.

No one has to fill out endless forms to fight with insurance companies about treatment options - this would be so stressful after a serious diagnosis, like my family had - January 2006 my DH was diagnosed with a brain aneurysm - which by the way had been misdiagnosed by a Boca Raton hospital team 3 weeks beforehand when he was rushed to the hospital while we were on vacation - then in Oct. 2006 my BC dx. I nearly had a nervous breakdown between these 2 very serious events occuring within months of each other - I cannot even begin to fathom the stress and pressure of having to justify treatment with an insurance company. And we got immediate treatment with top notch specialists at the hospitals we chose. Scans, tests etc. were scheduled by our doctors, we did not have to wait for "approval" from an insurance company.

all the best
caya (a content Canadian)
__________________
ER90%+/PR 50%+/HER 2+
1.7 cm and 1.0 cm.
Stage 1, grade 2, Node Negative (16 nodes tested)
MRM Dec.18/06
3 x FEC, 3 x Taxotere
Herceptin - every 3 weeks for a year, finished May 8/08

Tamoxifen - 2 1/2 years
Femara - Jan. 1, 2010 - July 18, 2012
BRCA1/BRCA2 Negative
Dignosed 10/16/06, age 48 , premenopausal
Mild lymphedema diagnosed June 2009 - breast surgeon and lymph. therapist think it's completely reversible - hope so.
Reclast infusion January 2012
Oopherectomy October 2013
15 Years NED!!
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Old 02-02-2008, 05:29 PM   #20
Patty F
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Caya
I agree with you. The insurance companies run the medical profession. After I was dignosed bt Dr. wanted me to have a breast MRI. The insurance company denied it. I just had surgery on Wednesday and my surgeon said he wanted another ct scan. I don't know if my insurance co will approve another one since the last one was only 3 months ago.
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