Saturday, December 20, 2014
So What!? Med copays go toward OOP Max
Tuesday, December 9, 2014
NC Mom Travels to Boehner’s Office to Deliver Message | Pundit House
Tuesday, December 2, 2014
Controversial Atheist Billboard: Girl's Christmas Wish is to Mis - WKRN News 2
The billboard doesn't offend me. I do, however, think it is stupid. They say they don't believe in "fairy tales" but then start the letter on the billboard with "Dear Santa". Which is it? Do they or do they not believe in fairy tales? Are they saying it is okay to believe in Santa but not to believe in Jesus? Why do they care so much? No one is forcing them to believe in Jesus, Santa or the tooth fairy, for that matter.
The information beliw is cut and pasted from this link. I've started cutting and pasting articles because I've found later, the links stop working or articles are moved, etc. Controversial Atheist Billboard: Girl's Christmas Wish is to Mis - WKRN News 2
Controversial Atheist Billboard: Girl's Christmas Wish is to Miss Church
Posted: Dec 01, 2014 6:23 PM ESTUpdated: Dec 01, 2014 6:49 PM ESTThe inflammatory billboards show a young girl writing a letter to Santa. The letter reads, “Dear Santa, All I want for Christmas is to skip church! I'm too old for fairy tales.”
The organization says of the billboards: The billboards are aimed at in-the-closet atheists who are pressured to observe religious traditions during the holidays, and who might also want to attend the annual American Atheists National Convention in Memphis in April.
In past years, similar billboards also sponsored by the American Atheists Association were placed in urban locations like New York City. This year, the group honed in on areas of the country known for strong religious beliefs: Memphis and Nashville Tennessee, St. Louis, Missouri and Fort Smith, Arkansas.
Reactions on the group's Facebook page varied from wholehearted support to disdain:
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American Atheists also said they tried to put up a billboard in Jackson, Mississippi but were rebuffed by lessors in the area.
What do you think of the billboards? How would you feel if one was erected in Richmond or another part of Virginia?
Sunday, November 23, 2014
SNL Slams Obama on Executive Amnesty
Saturday, November 15, 2014
Disabled Americans for Firearms Rights
Monday, November 10, 2014
#Obamacare Architect: We had to trick you to help you!
This will anger you. He even calls the American people stupid.
A FREE Way YOU Can Help My Family #Obamacare
Wednesday, November 5, 2014
Drug Coverage Cuts Endangered Sons' Lives: Opinion Piece
Pattie Curran is a North Carolina mother whose two sons receive treatment at Cincinnati Children’s Hospital Medical Center’s bone marrow clinic.
As the mother of two chronically ill children, our family has long faced high health care costs, and it’s getting worse, thanks to companies called pharmacy benefit managers.
My sons have a rare bone marrow failure condition called Shwachman-Diamond syndrome and have secondary mitochondrial disease. They require a broad range of medications to treat their life-threatening conditions, including compounded medications which are typically prescribed to patients who can't metabolize or tolerate commercial drugs.
By customizing prescriptions to the individual’s needs, doctors help patients like my sons, as well as patients dealing with the effects of cancer, diabetes and other serious conditions. Compounded drugs are also used by people with hormonal imbalances, chronic pain and allergies to certain ingredients in mass-produced medicines.
In July, I was notified that some of our sons' most important compounded medications are no longer being covered by Express Scripts. This is because Express Scripts – the nation’s largest pharmacy benefit manager, with 90 million Americans enrolled, according to the Associated Press –announced sweeping coverage cuts this summer to 1,000 ingredients used to make compounded medicines. The cuts are coming at the worst time for my sons, who, despite weekly trips to the ER and specialists, are trying to live normal lives filled with sports and after-school activities.
Today we find ourselves deeply in debt and drowning in the paperwork of what has become a full-time fight to restore coverage of essential, life-saving treatments for our sons. This year alone, we have been billed tens of thousands of dollars in out-of-pocket health care costs.
While some of the ingredients found in my sons’ compounded medications come in commercial form, there’s no FDA-approved medication or supplement on the market to treat mitochondrial disease. This alarms not only my family, but also my sons’ specialist. The specialist has written a letter to inform our insurance company that if my sons are not able to continue their compounded medications due to the lack of coverage, it could lead to neurodegenerative symptoms and potentially result in death.
As a mother this is devastating. I feel like I am at the mercy of pharmacy benefits managers and insurance companies.
Hundreds of thousands – perhaps millions – of Americans who use compounded medications face a loss or reduction in coverage as pharmacy benefit managers and insurance companies eliminate or severely limit coverage.
Patients and Physicians for Rx Access has formed to protect patient access to compounded medications. The coalition is made up of patients, advocacy groups, pharmacists, physicians, pharmacies and health care organizations focused on raising awareness about this crucial issue. By sharing information with patients and the doctors who are impacted by this unnecessary loss in benefits, the group hopes to fight these cuts.
Compounded medications have changed my sons’ lives, and it saddens me to know they and so many others face this new obstacle. Those most affected need to push back now and join the fight for compounded medication coverage to make an impact. Please visit www.saverxaccess.org to learn more.
Thursday, October 23, 2014
More Obamacare Destruction
Wednesday, October 22, 2014
Obamacare is More than Insurance Exchanges
Wednesday, October 15, 2014
$19,721.85
Wednesday, October 8, 2014
The Face Of Obamacare: Worry, Financial Devastation | Right Angles
The Face Of Obamacare: Worry, Financial Devastation | Right Angles
Tuesday, October 7, 2014
Picture: The Obamacare Effect on Families with Sick Kids
Monday, October 6, 2014
Open-enrollment Notice
My Interview on Fox & Friends
Saturday, October 4, 2014
Taxes in Obamacare that Impact My Family
Friday, October 3, 2014
My OpEd on Obamacare Appeared in The Washington Times
As the mother of two chronically ill children, I have long faced high health care costs. My sons suffer from a rare bone-marrow failure syndrome called Shwachman-Diamond syndrome and have secondary mitochondrial disease that requires treatment with a broad range of expensive medications. We averaged $10,000 to $12,000 a year in billed out-of-pocket medical expenses before Obamacare became law. In 2013, we incurred just over $27,000 in out-of-pocket medical expenses. President Obama’s signature piece of legislation has more than doubled our yearly medical costs.
Having read the then-proposed Affordable Care Act in 2010, I was skeptical of the legislation from the start. I knew that a vast expansion of government involvement in health care would create unintended consequences, and I publicly warned my own senator, Kay R. Hagan, North Carolina Democrat, about the impact the legislation would have on my children. Though she denied the truth of my claims at the time, almost everything I imagined would happen because of the law has come to fruition.
Prior to 2011, our insurance provider covered all of my sons’ treatments, surgeries and hospitalizations without one instance of a denied claim. I always considered our family very fortunate for the medical availability that we had before the law made its impact. As the founder of a nonprofit organization designed to support research and education for Shwachman-Diamond syndrome, I saw over the years the lack of medical access opportunity for families contacting me from Canada and England. They frequently reported difficulty obtaining necessary medications and even receiving routine diagnostic testing owing to denied coverage. One injectable medication my youngest son gets to boost his white blood cell count before surgery was denied to families in these countries because the medication was considered too expensive. Since Obamacare passed, what I saw happen to those other families is now happening to my own family right here in the United States.
With the imposition of new taxes and mandates as a result of Obamacare, employers and insurance providers have been forced to look for ways to cut costs. My husband’s employer is facing an increase of $7.4 million in health care expenses for 2014, alone owing to the mandates. We first noticed changes for our family in 2011. For us, it started with higher premiums, deductibles, out-of-pocket maximums and co-pays. The co-pay for a medication that protects my youngest son’s kidneys from damage had been $131 for a three-month supply for five to six years before the law passed. In 2011, the medication suddenly more than doubled. We watched in horror as it skyrocketed to $532 by the middle of 2013, while at the same time trying to get a medical-necessity exception. Obamacare not only made everything less affordable, it created more work for families and providers. We have witnessed a corresponding decrease in quality of care because of the extra administrative demands placed on physicians and their staff.
During the past month, some of our sons’ most important medications have been discontinued from coverage altogether. Their specialist wrote a letter to the insurance company to inform them that if my sons are not able to continue their medications owing to the lack of coverage, it could lead to neurodegenerative symptoms, which can result in death. Despite the clearly communicated consequences, we were informed that the insurance company could not file an appeal on our behalf until our plan changes (again). The president and Mrs. Hagan repeatedly told us, “if you like your plan, you can keep your plan.” We now know that is not true.
My husband has a good job, but it doesn’t pay nearly enough to cover all of the increased expenses. Yet he earns too much for us to qualify for relief programs from pharmaceutical companies because government regulations dictate who the private companies are allowed to help. His employer is burdened with extra financial costs because of the law. Employees are burdened and, as I’ve stated previously, physicians and their staff are burdened by the cumbersome mandates, as well.
Today we find ourselves deeply in debt and drowning in the paperwork of what has become a full-time fight to restore coverage of essential, lifesaving treatments for our sons. This year alone, we have been billed tens of thousands of dollars in health care costs out-of-pocket. Our credit cards are maxed out and our insurer, bound by rigid government rules, is unable to help us. Obamacare has been far from the salvation that was promised. For us, it has been nothing less than a nightmare of skyrocketing health care costs that threaten to bankrupt our family and keep our sons from receiving the lifesaving treatments they need.
Our situation has now become precisely what Obamacare supporters claimed they were trying to address. The policy debates in Washington have consequences in the real world — consequences that include losing access to lifesaving medications and treatments. These changes brought about by the law could have deadly consequences for my sons. Furthermore, if our family is dumped into the Obamacare exchanges, as we fear may happen, our children will lose access to the doctors who specialize in Shwachman-Diamond syndrome and mitochondrial disease. Mrs. Hagan’s deciding vote on Obamacare has meant disaster for our family and for families like ours. One-size-fits-all government programs, like Obamacare, will always have unintended consequences that will bring devastation to many American families.
Pattie Curran is a North Carolina mother of two children born with a rare bone-marrow dysfunction and founder of a nonprofit research and education organization related to the condition.
Read more: http://www.washingtontimes.com/news/2014/oct/2/curran-one-familys-obamacare-nightmare/#ixzz3ID1GGtjZ
Follow us: @washtimes on Twitter
Thursday, October 2, 2014
Obamacare Will Cancel 50,000 Plans before November
Wednesday, October 1, 2014
More Pre-Auths Required
BCBS of NC Plans
Tuesday, September 30, 2014
My Interview on Veiwpoints Today
Saturday, September 27, 2014
Others Harmed by Obamacare
Sunday, September 21, 2014
The Left Never Does Their Due Diligence
Thursday, September 18, 2014
The Left Came Out to Play
End the Export-Import Bank Rally at Kay Hagan's Office
Monday, September 15, 2014
Obamacare Leaves Family "Shocked and Horrified" by Medical Expenses | The Daily Sheeple
Team Twitchy first picked it up, then Daily Caller and The Daily Sheeple.
I am so thankful for the various media outlets that picked up the story of our family!
It's Official- Kids' Life-saving Meds No Longer Covered
Friday, September 12, 2014
Gianna's Cookbook!
I think you'll like it!