Showing posts with label mary bono mack. Show all posts
Showing posts with label mary bono mack. Show all posts

Thursday, April 15, 2010

Mary Bono Mack

I am working on having Congresswoman Mary Bono Mack visit one of our future meetings. I have made contact with her team and I should know something soon. P.S. I have already received a phone call from a person wanting info.

David Hines

Wednesday, September 2, 2009

Meeting with Congresswoman Mary Bono Mack's staff

I was able to meet with Mr. Marc Troast the District Director for Congresswoman Mary Bono Mack. It is my Hope and prayer that we can work together to help those suffering from the pain of peripheral neuropathy in its most cruel forms, that they may find help and Hope (in motion).

Monday, August 3, 2009

Advocacy groups push for passage of Medicare Patient IVIg Access Act of 2009

Get Involved!

Anyone can be an advocate—it is easy and important. IVIG is so important to so many people, but most members of Congress do not realize how many people rely on IVIG for their health. You can change that. You can tell them how much IVIG means to your health or to your loved one’s health.

A bill has been introduced in the House of Representatives and also in the Senate to help solve the problems many Medicare beneficiaries have getting IVIG where it is best for them: the physician’s office, the home or the hospital outpatient infusion center. These bills will not become law unless Congress hears from people like you all across the country. (Note: Congress often writes laws like this for Medicare beneficiaries because the federal government pays for Medicare. However, private insurance companies often follow Medicare policy, so these bills, if passed, can help the entire IVIG community.)

It takes just a few minutes to take action. First, click on the link below to find the three members of Congress who serve you: your one representative in the House and your two Senators. Then, after reviewing the material about the bills written to solve the problems for Medicare patients on IVIG, send an email to your members of Congress.

Thank you for your efforts!

Monday, June 8, 2009

Neuropathy advocacy includes political advocacy

Get involved and help us fight the good fight! I am native Californian and I want my state back! Meg Whitman is the right person for the job! Lets shake this state up and get some one who will balance the budget. Send Arnold packing. I have never seen a state that took from the disabled. I am a disabled American and I'm
not going to sit around and take it anymore. Get involved! Lets shake it up!

John McCain endorses Meg Whitman for California Governor 2010

Meg Whitman for Governor 2010!

Meg Whitman for Governor of Calif in 2010. This was taken in my neck of the woods.


">We stopped to take a pic in front of the wind turbines on I-1... on Twitpic

Meg Whitman for Governor 2010!

It was warm today in Redding, and I loved the area. Met with ... on Twitpic

Meg Whitman for Governor 2010!

Campaign HQ opens today in Silicon Valley. Exactly one year u... on Twitpic

Wednesday, May 27, 2009

Tuesday, May 19, 2009

The Christopher and Dana Reeve Paralysis Act

Washington, Jan 8 - Congresswoman Mary Bono Mack (R-CA) today joined Congresswoman Tammy Baldwin (D-WI) and Congressmen Jim Langevin (D-RI) and Gus Bilirakis (R-FL) in introducing the Christopher and Dana Reeve Paralysis Act, which will help improve the lives of and hasten better treatments and cures for people living with paralysis. “I am proud to join my colleagues in this bipartisan effort to enhance research on paralysis and improve quality of life for the many individuals living with this condition and other mobility impairments,” said Rep. Bono Mack. “The possibilities of medical science are endless, and as we look to bring help and healing to these individuals, it is essential that we coordinate research efforts on a national level and continue to work with organizations like the Christopher and Dana Reeve Foundation. Through this effort, we pay tribute to Christopher and Dana Reeve, who were tireless advocates on behalf of all people living with paralysis,” Bono Mack said. “We honor the activism of Christopher and Dana Reeve with this bipartisan effort to better treat and, we hope, cure paralysis and other serious motor impairments,” said Congresswoman Baldwin. “Chris and Dana used their visibility to work on behalf of families in all parts of the country who face the challenges of paralysis and impaired mobility. This legislation is part of their legacy and I’m hopeful that it will become law in this session of Congress,” Baldwin said. “The Christopher and Dana Reeve Foundation is extremely grateful to Representatives Tammy Baldwin, Mary Bono Mack, James Langevin and Gus Bilirakis for introducing this important legislation in Christopher and Dana’s honor. This critical initiative will advance research into cures and treatments for paralysis as well as improve the quality of life for those already living with the disability,” said Peter T. Wilderotter, President and CEO, Christopher and Dana Reeve Foundation. “Advancements are made every day in spinal cord injury research, but enacting the Christopher and Dana Reeve Paralysis Act will help to quickly and efficiently stimulate even more progress. We, at the Christopher and Dana Reeve Foundation, urge quick passage of the Act in Congress,” Wilderotter said. The legislation, named for the actor who was paralyzed in a riding accident and his wife who turned adversity into activism, seeks to avert redundancies and encourage collaborative research in paralysis and improving the quality of life for people living with paralysis and mobility impairments from any cause -- stroke, ALS, spinal cord injuries, and others. In the last session of Congress, the bill passed the House of Representatives, but failed to advance in the Senate. All four members of Congress pledged to work diligently to ensure that the bill becomes law this year. “I am pleased to join my colleagues in a renewed effort to pass this legislation in the 111th Congress. It is critical to help people with disabilities achieve and maintain their independence and to ensure that we are using the best research and technology to improve their quality of life,” said Rep. Langevin, who is the only spinal cord injured Member of Congress. “On a personal note, Chris and Dana were dear friends and it is now up to all of us to move forward and continue their legacy by seeing this bill signed into law,” Langevin said. “I am proud to be an original co-sponsor of this vital legislation and am happy to see that it is garnering bi-partisan support at its inception,” said Congressman Bilirakis. “Unfortunately, millions of Americans suffer from paralysis and mobility impairment. These individuals struggle each day to perform even the most basic of tasks that many of us take for granted. The economic and emotional impact this impairment has on their lives, and the lives of those who care for them, is staggering. I urge all my colleagues in the House to work together to pass this bill so America can make a comprehensive, coordinated effort to further advance paralysis research,” Bilirakis said. The Christopher and Dana Reeve Paralysis Act has three components that support and enhance paralysis research, rehabilitation, and quality of life programs: • Paralysis Research - Expands research on paralysis at the National Institutes of Health (NIH). This will encourage collaborative research by connecting scientists conducting similar work to further enhance understanding and speed discovery of better treatments and cures. • Paralysis Rehabilitation and Care - Builds on research to enhance daily function for people with paralysis including a Clinical Trials Network to measure effectiveness of certain rehabilitation tactics and encouraging shared findings on paralysis to improve rehabilitation. • Improving Quality of Life for Persons with Paralysis and Other Physical Disabilities - Works with the Centers for Disease Control and Prevention (CDC) to improve the quality of life and long-term health status of persons with paralysis and other physical disabilities.