Unless you have a keen interest in health policy - or you've had a personal experience in recent years - you probably haven't spent much time thinking about specialty tiers in health plan formularies. While not exactly dinner conversation in most circles, it's important for people to realize how a specialty tier can put patients' health at risk. Why? It restricts access to needed treatments.
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There's some huge news in brain research today: Microsoft co-founder Paul Allen just pledged $300 million to the Allen Institute to promote open-science research on brain circuitry. That donation will help to double the Allen Institute's staff and fund the first four years of a ten-year project, whose plans for "brain observatories" read like something out of a science fiction movie.
For me certain things seem to happen every day.
This morning, I lost someone dear to me to cancer.
He isn't the first person I've lost, nor will he be the last, I'm afraid.
In healthcare, there's a pretty common phrase: "a cure for cancer." But when you watch someone you love go through it, you understand that there's no such thing. There are thousands of cancers and each one attacks the body differently. Because of this, there can be no common cure.
Recently, I spent a few moments watching an interview with author and consultant Simon Sinek, in which he defines innovation and "the application of technology to solve human problems."
The latest Congressional Budget Office (CBO) spending estimates show, once again, that the Medicare prescription drug benefit's competitive, market-based structure is leading to much lower than expected overall program costs - while continuing to deliver medicines to seniors at affordable costs.
A recent article in Newsweek brought to light to an interesting project, spearheaded by a Long Island Alzheimer's researcher Peter Davies, to sequence the entire genome of about 1,000 Alzheimer's patients over the next three to four years.
Dr. Patricia Robinson, an African American oncologist in Chicago, certainly captured the attention of reporters at a recent roundtable on clinical trials of new medicines attended by journalists from Chicago-area Latino American, African American and Asian American community newspapers.
More than half of Americans doubt this country's ability to keep global research and development leadership. That was the focus of the Research!America forum I attended yesterday with PhRMA President & CEO John Castellani.
Along with this year's must-pass reauthorization of the Prescription Drug User Fee Act, it is also time to reauthorize the Best Pharmaceuticals for Children Act (BPCA) and Pediatric Research Equity Act (PREA), which are intended to increase research conducted about use of medicines in children. We hope that Congress will permanently reauthorize this legislation, which will provide the certainty needed to encourage companies to embark on years-long pediatric studies.
Later today, PhRMA President & CEO John Castellani will be participating in Research!America's annual National Health Research Forum: World Class to 2nd Class -- Confronting the Risks to U.S. Science and Innovation.
Writer Carl Zimmer had a thought-provoking book review in The Wall Street Journal over the weekend.
There are some more warning signs today of the incredible cost of dementia to both patients and our economy.
We continue the conversation of rare diseases as a global health challenge with Lundbeck's Dr. Christopher Silber. Offering effective therapies is a fundamental component of the commitment to help improve the lives of people with challenging, unmet medical needs. At Lundbeck the focus is on making a difference for patients, no matter how complex the condition.
What compelled you to join the fight against rare diseases?