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Celebrating a storied tradition of clinical care, education and research
The UAB Division of Pulmonary, Allergy, and Critical Care Medicine was founded in 1955 by Ben Vaughan Branscomb who served as its Director until 1970. Dick Dowling Briggs, Jr. (Division Director, 1971 – 1992) succeeded Dr. Branscomb and continued to build on the strong foundation set by him to develop the Division into one of the premier programs in the country.
To celebrate the legacy and contributions of Drs. Branscomb and Briggs, the Division established the inaugural Branscomb-Briggs lectureship on March 5, 2010 at UAB. The first lecturer was Dr. Stephen Rennard, Larson Professor of Medicine in the Pulmonary and Critical Care Medicine Section at the University of Nebraska Medical Center. Dr. Rennard’s lecture on “COPD in the Emerging Era of Personalized Medicine” was well received by all, including the honorees who are also his close friends. The evening celebration shifted to the Harbert Center where Drs. Branscomb and Briggs were “toasted and roasted” by former fellows, colleagues, and friends. The event was attended by over 100 guests from Birmingham and surrounding communities, many who were trainees under these former Division Directors.
The Division has continued to grow under the subsequent leadership of K. Randall Young, Jr. (1992-2007), James E. Johnson (2007-2009; Interim Director), and Victor J. Thannickal, the current Division Director. The Division currently holds 36 full-time faculty members with a primary appointment in the Department of Medicine. The Division is committed to excellence in clinical care, integrated approach to education, and innovative research.
Excellence in Clinical Care – Focus on Critical Care
The Division is responsible for the care of critically ill patients in our Medical Intensive Care Unit (MICU), hospitalized patients in a dedicated pulmonary in-patient service (6-South), and consultant support for patients on other wards and ICUs. All of our clinical faculty see ambulatory patients in the Kirklin Clinic, accounting for over 12,500 patient visits per year. Other specialized services include diagnostic and interventional bronchoscopy services, pulmonary function testing, cardiopulmonary exercise testing, sleep-wake disorders center, and specialized clinics related to cystic fibrosis, lung transplantation and interstitial lung disease. We are working with the UAB Health System in expanding these specialized “pulmonary service lines” as well as in providing comprehensive and coordinated care for critically ill patients in our ICUs.
The MICU currently carries three housestaff teams with thirty to thirty five critically ill patients at any given time. These patients have a variety of illnesses, including acute respiratory failure, severe sepsis, acute respiratory distress syndrome, renal failure and cardiac failure. Protocols have been implemented to ensure that patients consistently received evidence-based care. Patients with severe infections are managed with a sepsis protocol. Patients on mechanical ventilators are managed with a lung-protective ventilator strategy. Patient safety interventions are employed and measured for compliance. These include prophylaxis for venous thrombosis, gastrointestinal bleeding and a bundle of interventions for prevention of ventilator-acquired pneumonia and central line infections. Adherence with all of these exceeds the goal of 90%. The MICU rotation has repeatedly been selected by internal medicine residents as being among the best educational experiences of their inpatient rotations.
Integrated Approach to Education
The Division is committed to training the next generation of pulmonary and critical care specialists by ensuring the acquisition of requisite diagnostic and procedural skills in the evaluation and management of patients with pulmonary disorders and critical illness. The Division has a history of outstanding teaching with numerous awards from the Department of Medicine. Over the past year, a number of new faculty have been recruited to the Division who have expanded the educational activities in interventional bronchoscopy and interstitial lung disease. The Division’s educational mission benefits greatly from the wide range of expertise among the faculty in the areas of airways disease, including COPD, asthma and cystic fibrosis, lung transplantation, bronchoscopic procedures (e.g. endobronchial ultrasound-guided biopsies), and sleep disorders. The educational mission also benefits from the inter-disciplinary interactions with teaching faculty in the Departments of Pathology, Anesthesiology, Radiology and Surgery.
Scholarship and research is expected during fellowship training and faculty mentorship is fostered. Two training tracks – the Clinician-Educator and Physician-Scientist – have been implemented to facilitate this goal. Recent and current fellows have pursued graduate degrees through the Department of Public Health and the Department of Physiology and Biophysics. An NIH T32 Training Grant in Lung Biology and Translational Medicine was submitted this year to facilitate the development of physician investigators.
Innovation in Research
Research in the Division spans studies on basic cellular/molecular and immunologic bases for lung disease, translational approaches in biomarker/drug discovery, and clinical trials for patients with sepsis, IPF, CF, and COPD. Total research funding in the Division is now over $8.8 million per year, which represents a more than doubling of funding during the previous year. Here, we highlight research in the laboratories of Dr. Chad Steele and Dr. Ed Blalock.
Research in the Dr. Steele laboratory is broadly based in lung immunology and host defense. A particular focus of the laboratory is on understanding myeloid cell-mediated innate immune responses against opportunistic fungal pathogens that cause life-threatening lung infections in immunocompromised individuals with such diseases as HIV, COPD and leukemia. Dr. Steele’s research on the fungal pathogen Pneumocystis carinii has uncovered a novel Src tyrosine kinase signaling pathway that regulates the magnitude of the lung inflammatory response as well as change the pattern of alveolar macrophage activation. This pattern of macrophage activation, termed M2a, is associated with more efficient elimination of P. carinii from the lungs, yet has not been described in P. carinii host defense. Dr. Steele’s research team is currently characterizing multiple M2a-associated innate host defense molecules in an effort to understand what influences alveolar macrophage effector responses against P. carinii. The overarching goal of this work is to uncover new innate immune pathways that can be therapeutically augmented in the setting of immunosuppression and immunodeficiency for the treatment of P. carinii pneumonia. In a second project, Dr. Steele’s research team has discovered an essential role for a myeloid-associated fungal recognition receptor, Dectin-1, in lung innate immune responses to the fungal pathogen Aspergillus fumigatus. Dectin-1, which recognizes beta-glucan carbohydrates found in the cell wall of all medically-important fungi, controls the production of multiple inflammatory cytokines, including IL-17. Dr. Steele’s lab has recently reported a role for IL-17 in A. fumigatus lung defense and has recently been awarded a 2-year ARRA R01 and a new, 4-year R01 focusing on the lung cell source of IL-17, which pathways drive the development of this cell population and the downstream IL-17-associated mechanisms that promote elimination of A. fumigatus from the lungs.
Research in the Blalock group has focused on pathways of pulmonary inflammation. Specifically, Dr. Blalock and colleagues have described a novel neutrophil chemoattractant, proline-glycine-proline (PGP), in chronic inflammatory lung disorders. In addition, this group has also determined the specific proteolytic cascade involved in PGP liberation from collagen, highlighting numerous potential therapeutic targets in this unique inflammatory pathway. This work has been published in Nature Medicine, Journal of Immunology, and Journal of Neuroimmunology. In more recent work (under review at Science), Dr. Blalock and Wellcome Fellow, Dr. Rob Snelgrove, in collaboration with pulmonary faculty members Drs. Amit Gaggar, Pat Jackson, and Steve Rowe, have demonstrated a novel endogenous anti-inflammatory pathway for PGP. This work focuses on the enzyme, leukotriene A4 hydrolase (LTA4H), which is known to generate the pro-inflammatory molecule, leukotriene B4 (LTB4) via its hydrolase activity. In contrast, the Blalock group discovered that the aminopeptidase activity of LTB4 mediates anti-inflammatory effects by degrading PGP. These findings have implications for therapeutic strategies that target LTA4H to prevent LTB4 generation since this may inadvertently lead to elevations in PGP and neutrophilic inflammation. This work was made possible through a state-of-the art Pulmonary Proteomics facility and Drug Discovery Program affiliated with the UAB Lung Health Center. Dr. Blalock will be honored with the Max Cooper Award for Excellence in Research for 2010 at a reception to be held on Tuesday, May 25, 2010.
Separate, Retrospective SPIRIT IV Cost-Effectiveness Analysis Presented Earlier this Year Concludes XIENCE V Is Economically Dominant Compared to TAXUS
ABBOTT PARK, Illinois, May 5, 2010 - Findings from Abbott's SPIRIT IV trial, one of the largest randomized
clinical trials comparing two drug eluting stents, with 3,690 U.S.-based
patients, were published today in The New England Journal of Medicine. The
published study results show that one year after a stenting procedure,
patients treated with Abbott's market-leading XIENCE V(R) Everolimus Eluting
Coronary Stent System were significantly less likely to have a major adverse
event such as a heart attack, repeat procedure or cardiac death, compared to
patients treated with a TAXUS(R) Express2(TM) Paclitaxel-Eluting Coronary
Stent System (TAXUS). The SPIRIT IV trial also showed that patients treated
with XIENCE V were considerably less likely to experience a blood clot (stent
thrombosis) compared to patients treated with TAXUS. These results were
originally presented during the September 2009 Transcatheter Cardiovascular
Therapeutics (TCT) conference.
In the SPIRIT IV trial's primary endpoint of target lesion failure (TLF),
XIENCE V demonstrated a statistically superior 38 percent reduction compared
to TAXUS at one year (4.2 percent for XIENCE V vs. 6.8 percent for TAXUS,
p-value=0.001). TLF is defined as a composite measure of important efficacy
and safety outcomes for patients and includes cardiac death, heart attack
attributed to the target vessel (target vessel myocardial infarction), and
ischemia-driven target lesion revascularization (TLR). The SPIRIT IV trial
also found that the one-year rate of blood clots (stent thrombosis) with
XIENCE V is among the lowest reported to date with any drug eluting stent
(0.29 percent per Academic Research Consortium definition of
definite/probable stent thrombosis).
In a subgroup analysis of more than 1,100 patients with diabetes, who
typically are sicker and have more challenging artery disease, XIENCE V
demonstrated a numerically lower TLF rate compared to TAXUS at one year (6.4
percent for XIENCE V vs. 6.9 percent for TAXUS, p-value=0.80). In the
critical safety endpoint of stent thrombosis as presented during TCT 2009,
XIENCE V demonstrated a 40 percent reduction compared to TAXUS in patients
with diabetes (per ARC definition of definite/probable stent thrombosis, 0.80
percent for XIENCE V vs. 1.33 percent for TAXUS, p-value=0.52).
"With more than 3 million stent procedures being performed annually
worldwide, determining the safety and efficacy differences between various
drug eluting stents has important implications for societal health," said
Gregg W. Stone, M.D., professor of medicine at Columbia University Medical
Center; immediate past chairman of the Cardiovascular Research Foundation in
New York; and principal investigator of the SPIRIT IV trial. "With nearly
4,000 patients studied, SPIRIT IV represents the largest randomized trial of
two drug eluting stents completed to date, and found that the
everolimus-eluting stent significantly reduces a patient's risk of
experiencing a heart attack, stent thrombosis, or the need for a repeat
procedure within one year, compared to the paclitaxel-eluting stent. Based on
these results, and results from the 1,800-patient COMPARE study conducted in
the Netherlands, the everolimus-eluting stent has set a new standard for
patient safety and efficacy."
Separately, in a recent retrospective cost-effectiveness analysis of
SPIRIT IV data, researchers found that the clinical benefits offered by
XIENCE V translated into lower overall medical costs at one year after the
stenting procedure. The SPIRIT IV cost-effectiveness analysis, presented by
David Cohen, M.D., MSc, of St. Luke's Mid America Heart Institute in Kansas
City, Mo., in March 2010 at the Optimizing PCI Outcomes symposium sponsored
by the Cardiovascular Research Foundation, found that one-year total medical
costs (initial hospitalization plus follow-up) were approximately US$150
lower for patients treated with XIENCE V than those treated with TAXUS. When
costs not related to the original treated vessel (
non-target-vessel-revascularization) were excluded, the one-year medical
costs were approximately US$450 lower with XIENCE V than TAXUS. The XIENCE V
and TAXUS stents are competitively priced.
"The cost-effectiveness analysis of SPIRIT IV shows that a stent designed
to deliver outstanding clinical benefits can deliver economic benefits as
well," said Dr. Cohen, who is the lead investigator of the SPIRIT IV
cost-effectiveness analysis. "Since the findings were derived from a
multicenter, comparative trial with only clinical follow-up, these results
may be generalizable to most U.S. practice settings."
"The SPIRIT IV data, published today in The New England Journal of
Medicine, have changed clinical practice as more and more physicians around
the world have embraced the XIENCE V drug eluting stent. With the additional
SPIRIT IV cost-effectiveness analysis, we have observed favorable economic
data based upon the strong clinical results. These findings should prove
valuable as hospitals evaluate different treatment options for coronary
artery disease patients," said Charles A. Simonton, M.D., FACC, FSCAI,
divisional vice president, Medical Affairs, and chief medical officer, Abbott
Vascular.
More About SPIRIT IV Results
Clinically, in addition to demonstrating superiority in the primary
endpoint of TLF, XIENCE V demonstrated a statistically significant 46 percent
reduction in TLR (repeat procedure) compared to TAXUS at one year (2.5
percent for XIENCE V vs. 4.6 percent for TAXUS, p-value=0.001). TLR is one of
the major secondary endpoints of the SPIRIT IV trial.
Per protocol definition of stent thrombosis (blood clots) at one year,
XIENCE V demonstrated an observed 80 percent reduction compared to TAXUS
(0.17 percent for XIENCE V vs. 0.85 percent for TAXUS, p-value=0.004). Per
Academic Research Consortium (ARC) definition of definite/probable stent
thrombosis, XIENCE V demonstrated an observed 74 percent reduction compared
to TAXUS at one year (0.29 percent for XIENCE V and 1.10 percent for TAXUS,
p-value=0.004). The ARC definitions of stent thrombosis were developed to
harmonize the definition of stent thrombosis across various drug eluting
stent trials.
In a retroactive look at the economics of using XIENCE V versus TAXUS
from the SPIRIT IV trial, it was observed that XIENCE V was economically
dominant over TAXUS based upon the clinical results. At one year, total
medical costs (initial hospitalization plus follow-up) were US$146 lower per
patient with XIENCE V than with TAXUS. When costs not related to the original
treated vessel (non-target-vessel-revascularization) were excluded, the
difference between the two stents became more pronounced, amounting to a cost
savings of US$439 per patient with XIENCE V compared to TAXUS (p=0.02).
Excluding the costs not related to the original treated vessel reflects the
cost difference specific to the performance of the two stents.
The SPIRIT IV cost-effectiveness analysis was based on a retrospective
review of prospectively collected medical resource utilization for all
patients enrolled in the SPIRIT IV trial for initial hospitalization and one
year after enrollment. Cardiovascular hospitalizations, revascularization
procedures, diagnostic catheterization and dual-anti-platelet therapy costs
were included. The analysis assumed equal stent costs for the XIENCE V and
TAXUS stents.
More About XIENCE V
Abbott's market-leading XIENCE V is used to treat coronary artery disease
by propping open a narrowed or blocked artery and releasing the drug,
everolimus, in a controlled manner to prevent the artery from becoming
blocked again following a stent procedure.
XIENCE V is built upon Abbott's market-leading bare metal stent, the
MULTI-LINK VISION(R) Coronary Stent System. The VISION platform is designed
to facilitate ease of delivery, making it easier for physicians to maneuver
the stent and treat the diseased portion of the artery.
In some geographies, Abbott supplies a private-label version of XIENCE V
to Boston Scientific called the PROMUS(R) Everolimus-Eluting Coronary Stent
System. PROMUS is designed and manufactured by Abbott and supplied to Boston
Scientific as part of a distribution agreement between the two companies.
Everolimus, developed by Novartis Pharma AG, is a proliferation signal
inhibitor, or mTOR inhibitor, licensed to Abbott by Novartis for use on its
drug eluting stents. Everolimus has been shown to inhibit in-stent neointimal
growth in the coronary vessels following stent implantation, due to its
antiproliferative properties.
XIENCE V is indicated for improving coronary luminal diameter in patients
with symptomatic heart disease due to de novo native coronary artery lesions
(lesions less than or equal to 28 mm). Additional information about XIENCE V,
including important safety information, is available online at
www.xiencev.com or
www.abbottvascular.com/en_US/content/document/eIFU_XienceV.pdf.
About Abbott Vascular
Abbott Vascular is a global leader in cardiac and vascular care with
market-leading products and an industry-leading pipeline. Abbott Vascular
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About Abbott
Abbott (NYSE: ABT) is a global, broad-based health care company devoted
to the discovery, development, manufacture and marketing of pharmaceuticals
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company employs more than 83,000 people and markets its products in more than
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Abbott's news releases and other information are available on the
company's Web site at www.abbott.com.
Media, Jonathon Hamilton, +1-408-845-3491, or Jennie Kim, +1-408-845-1755, or Financial, Larry Peepo, +1-847-935-6722, or Tina Ventura, +1-847-935-9390, all of Abbott








April 18, 2010 at 5:58 pm
Oh and Chris, there are pictures of CHeney and Rumsfeld shaking the hand of Saddam Hussein and his cronies.
Have fun choking because that rather shoots down any sense of superiority you get claiming making up stupid claims about Obama and Chavez.
April 18, 2010 at 5:57 pm
Chris wrote:
Bush was a humble person, a faithful husband, a dignified person in general.
He was arrogant and egotistical.
And as for “faithful husband” that has what to do with being President? No matter what you say he was one of our worst Presidents of all time.
Bush authorized a fools war in Iraq that did no small part in nearly bankrupting this country. He attacked Iraq despite them having nothing to do with 9-11. He let Osama bin Laden get away and he did little to deal with Al Qaeda. He authorized torture. He sacrificed much of our moral standing with the rest of the world. And domestically he continously screwed over the middle class and the poor while kissing the asses of the rich.
And you want to claim that Kennedy’s alleged affairs makes him a worse person then Bush? My..you do have a messed up sense of morality. Let me know when you want to bother to have an actual sense of morality. Because thinking that a person who cheated on his wife is worse morally then a person who ordered torture is just this side of being morally depraved.
April 18, 2010 at 3:02 pm
Historians are just liberal elitist pricks who look back at history and form an opinion on it. They don’t look at history any more objectively than they look at the present day. “Historian” is just a title given to someone with a hobby in reading history books. And those historians are just using W. as a scapegoat; there was that one American president (I forget his name) who lasted one month in the presidency. He got nothing done in that one month, needless to say, so you would think any objective “historian” would call him the worst. But the “historians” obviously based their conclusion on Bush being the worse simply because they didn’t like him.
“A loophole or gap in a law is common, and not a sign of incompetence.” Oh, okay. I’d have to argue that incompetence is common, then. (Well, that goes without saying when it’s in regard to Congress.)
“If insurance companies deprive coverage,…there will be litigation.” They wouldn’t be breaking any laws by denying coverage to anyone, because the law doesn’t say they can’t. I’m not saying they should deny coverage, of course, but looking at it objectively, they have that right. But I see you’ve jumped on the insurance-companies-are-evil bandwagon, even though they make only 3% profit.
“Unless Sauron is more effective in mustering Republicans against an amendment than he was the first time around. It would be a heckuva fight, with pro-life Republicans publicly repudiating their stands in order to force children to suffer and die.” It wasn’t just Republicans who were against the health-care takeover; Republicans were, Democrats were, and Independents were. And come on, guy, that’s a tad dramatic, “The Republicans want to force children to suffer and die!” Oh, okay.
“…The provision Sen. Feinstein had proposed to fix the problem was stopped by Republican.” Republicans against have not once tried to stop reform, and the Democrats who supported the health-care takeover have not once tried to initiate reform. The new bill does nothing to reform anything. It doesn’t increase competition because it still prevents you from purchasing insurance across state lines. There’s no malpractice-suit reform in there. Republicans offered numerous solutions while the Democrats literally locked themselves up behind closed doors to prevent the Republicans from having any part of the legislation. So, yes, the Republicans should be proud that they tried to prevent socialism and offered up true reform.
“It will be interesting to see how recalcitrant industries fight improved health care. The important first step in reining in costs was to expand coverage.” Coverage was expanded to some 10 or 15 million people at the expense of freedom and at the expense of reducing the quality of the health care to everybody else. Yay.
“Occasional wins by evil is not evidence that the war has been lost.” Good, this gives me some hope.
April 18, 2010 at 2:50 pm
You’ve never met Bush, and you don’t know much about him, do you.
April 18, 2010 at 2:47 pm
Good friends with Chavez? They’ve met once. Obama said Venezuela needs to get with the program, stand up for rule of law in the Americas. Chavez gave Obama a book.
You imagine a lot that didn’t happen and isn’t realistic. Obama’s no closer to Chavez than Dick Cheney is, just wiser in handling the nut.
Who cares what Castro says in an interview? Castro didn’t claim Obama’s anything other than a U.S. flag-waving patriot. I can’t find anything that suggests Castro approves of Obama’s policies, especially since Obama turned up the diplomatic heat on Chavez. What are you talking about?
April 18, 2010 at 2:21 pm
And apparently I suck at HTML.
April 18, 2010 at 2:18 pm
Nick Kelsier:
Yes, because W. cheated on his wife with countless women and thought he could do whatever he wanted just because he was the president. Bush was a humble person, a faithful husband, a dignified person in general.
Yes, because Saddam Hussein wasn’t a brutal dictator who killed hundreds and hundreds of thousands of his own people. The world is safer because that madman is dead. Because BUSH got rid of him. Hussein DID have WMDs (he used them against his own people, duh). The only thing Bush made a mistake at was warning Iraq that we were coming (the UN approved of the invasion, by the way, as did Congress). Because we warned Hussein (Saddam, not Obama), he was able to get the WMD over the border to Syria. We should have just gone in there with no warning. And we need to do the same to Iran, but Obama’s a weak rookie who likes to appease and pal around with dictators (he’s good friends with Chavez, and even Castro–former communist dictator of Cuba–approves of the way Obama is running America. Communists don’t approve of democracy, yet this communist approves of Obama’s job. Interesting, no?
Yeah, poor terrorists, being “tortured,” boo-hoo. We made blood-thirsty psychopaths THINK they were drowning, oh man, so harsh, so, so evil! Poor terrorists!
Now, I can’t WAIT for you to tell me how Bush “crashed the economy.” I can’t wait. Please tell me, seriously. Don’t hold back. Tell me what you think.
You:
You mean like Obama is doing now? On both counts? Kinda like that? Why are liberals so anti-rich? People get rich because they earned it. They get rich because of hard work and ambition, most of the time. Other times they inherit it, sure, but the majority of the time, they earned it. Jealous? Then try harder like they did. Don’t steal from them to pay for your unambitious, whiny self.
April 18, 2010 at 11:24 am
Ed writes:
It would be a heckuva fight, with pro-life Republicans publicly repudiating their stands in order to force children to suffer and die.
Really think they’re going to have much of a problem doing that, Ed? It’s not like they’ve shown much concern for the health and life of children after they’ve been born so far….
Claiming the Republicans are “pro-life” is like claiming that David Duke is pro-black.
April 18, 2010 at 10:13 am
Health care legislation as Waterloo – Oliphant (and Benson …
April 18, 2010 at 1:24 am
Not liberals based on polls who said Bush was worst ever: Historians, based on their comparison with every other president. (It’s a Rolling Stone story, and their website is down this weekend for dramatic revisions.)
A loophole or gap in a law is common, and not a sign of incompetence. It’s quite inventive of the insurance companies to claim to have found a way to deprive sick and injured children of coverage. I’m sure you read the article carefully. If insurance companies deprive coverage, contrary to the language of the conference report, there will be litigation. If by some fluke the insurance companies win that litigation, proving that Congress’s intent was not carried out in the language they passed, there will be amendments, unless Sauron is more effective in mustering Republicans against an amendment than he was the first time around. It would be a heckuva fight, with pro-life Republicans publicly repudiating their stands in order to force children to suffer and die.
The new law has protections of consumers built in, to resolve and head off some of the problems you fear, according to the NYT article (by my old friend Robert Pear, who is among the best in covering these issues):
Will insurance premiums rise? We were sure of it before, at about a 15% per year clip. Does the LA Times article say they will rise faster than that? It notes that the provision Sen. Feinstein had proposed to fix the problem was stopped by Republican’s obstreperousness (“Congressional rules” is what the article said). Republicans won’t be proud to trumpet this one, either, I’ll wager. We needed a good gross of Righty-Be-Gone to fix that problem (Why didn’t you note that it was the right that cause this problem? Are you ashamed of it, too?)
It will be interesting to see how recalcitrant industries fight improved health care. The important first step in reining in costs was to expand coverage. A public option to compete with insurance companies might have provided a good, market mechanism to fight undue increases, but since the Republicans have not allowed that yet, we’ll probably have to go the regulatory route.
Ironic that Republicans are driving increased regulation of private industry, no? Unprincipaled, unholy opposition to good government will create such problems, and every Republican should hang his or her head in shame.
My God is not incompetent. Evil is not benign, though, and must be fought at every turn, at every moment. Occasional wins by evil is not evidence that the war has been lost.
WordPress and HTML: Yeah, HTML is accepted at almost all WordPress powered blogs, and all WordPress hosted blogs that I have found. Good luck with your blog.
April 18, 2010 at 12:23 am
Anything Kennedy did as far as being a “disgusting human being” pales to W, Chris.
Least Kennedy didnt start a fools war in a country that did nothing to deserve invaded. At least Kennedy didn’t authorize torture. And at least Kennedy didn’t crash the economy, screw the middle class and suck the dicks of the rich.
April 17, 2010 at 10:42 pm
I agree with you about Truman. He’s just about the only Democrat I like. He made unpopular decisions that saved millions of lives (and not only the lives of Americans). And aside from being a disgusting human being, Kennedy was not too bad a president. Remember when you liberals pointed to Bush’s approval ratings (and still do) and said, “See? He’s the worst president in history”? Yeah.
Now, I’m glad you brought up this “no pre-existing conditions” thing. It was reported in the New York Times, one of Obama’s many personal fluffers, that while ObamaCare DOES prevent children from being DROPPED from coverage because of a discovered pre-existing condition, it does NOT prevent insurance companies from DENYING coverage to children with pre-existing conditions. That’s what happens when, in a mad rush to advance pure Marxism, you push through legislation before even taking time to proofread it, let alone read it at all. Remember what Pelosi said? “We have to pass the bill so you can see what’s in it.”
And just for kicks, from the LA Times, one of the most liberal, in-the-can-for-Obama publications around, we find this:
“Public outrage over double-digit rate hikes for health insurance may have helped push President Obama’s healthcare overhaul across the finish line, but the new law does NOT give regulators the power to block similar increases in the future.
“And now, with some major companies already moving to boost premiums and others poised to follow suit, millions of Americans may feel an unexpected jolt in the pocketbook.
“Although Democrats promised greater consumer protection, the overhaul does NOT give the federal government broad regulatory power to prevent increases.
“‘It is a very big loophole in health reform,’ Sen. Dianne Feinstein (D-Calif.) said. Feinstein and Rep. Jan Schakowsky (D-Ill.) are pushing legislation to expand federal and state authority to prevent insurance companies from boosting rates excessively.”
Your gods are completely incompetent.
Also, from one decent human being to another, I just made my WordPress blog last night and am still unsure of a bunch of things, one of which is whether or not I can use basic HTML in comments like this. Do you happen to know? I didn’t want to try it and then have my comment end up looking like crap because HTML is NOT accepted. There’s no preview button, so I figured I shouldn’t risk it.
April 17, 2010 at 10:07 pm
Like Truman, sometimes you pay a public poll price for doing the right thing. Still have to do the right thing.
Wait until the Republicans start campaigning on repeal of the “no pre-existing condition” clause. I can hardly wait.
April 17, 2010 at 9:37 pm
Meanwhile, his poll numbers keep falling….