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Archive for August 2009 – Page 2

After a Meeting with Your Congressman or Senators

Posted: August 10th, 2009 | By: Staff | No Comments
Monday, August 10th, 2009

Thank you for taking the time out of your busy schedules to meet with your Congressman and/or Senators! We appreciate your advocacy and leadership with the SMA Treatment Acceleration Act, as the value of a face-to-face meeting is incomparable.

After your meeting, follow-up is extremely important. Please send a brief recap of your meeting to Caroline Gibson, FightSMA Public Affairs Coordinator (carolinegibson@fightsma.com). Be sure to include the name and email (if applicable) of any staff members that were present in the meeting. Caroline will pass on your notes and work with our government affairs team on the ground in Washington. They will follow-up with the appropriate legislative aide in your Members’ Capitol Hill offices.

Another important thing to do after your meeting is to get the word out to other SMA families to let them know that you met with your Member(s). You can “tweet” on Twitter about your meetings, though we do ask you to limit your tweets to the fact that you met with an office and are encouraging others to do the same. Please do not publicly characterize meetings or include staff names or specific statements by Members or staff. A sample “tweet” would be:

I met with my Members of Congress asking them to support the SMA Treatment Acceleration Act. Have you?

You can also append a link to the FightSMA website for more information.

You can update your Facebook status with the message “I Met With My Members of Congress to Support the SMA Treatment Acceleration Act! Get help scheduling a meeting with your Members by clicking here! http://www.fightsma.org/index.php?congressional_info.” Again, we request a level of discretion about your private meeting when publicly encouraging your friends, family, and colleagues to meet with their Members on behalf of the bill, too.

If you have any questions at all, please call Caroline Gibson at 804-515-0080 or email at carolinegibson@fightsma.com.

Thank you all for all you do for the fight against SMA!

Comments (0)
Categories : SMA Treatment Acceleration Act

Important Message to SMA Families: August Grassroots Call to Action

Posted: August 5th, 2009 | By: Staff | No Comments
Wednesday, August 5th, 2009

Dear Friends,

We are well under way with our efforts on the SMA Treatment Acceleration Act. As you know, the bill was reintroduced in the 111th Congress in April by our lead sponsors: Rep. Patrick Kennedy (D-RI) and Rep. Eric Cantor (R-VA) in the House, and Sen. Debbie Stabenow (D-MI) and Sen. Johnny Isakson (R-GA) in the Senate.

As you are probably well-aware, both houses of Congress have been focused on Health Care Reform over the past several months. The Health Care Reform bills have required a tremendous amount of focus, attention, and effort from our Members of Congress, as well as health staffers, on both sides on the aisle. We have been told by multiple health staffers that they have been inundated with emails, meetings, and health care reform related work that has made it virtually impossible to steer their focus to any other issue at this time.

While we applaud the efforts of our Members of Congress for the incredible amount of care and attention put towards health care reform, it does mean that we, as supporters of the SMA Treatment Acceleration Act, are playing a different “ballgame.”

With the arrival of Congress’s month long August recess, it is more important than EVER that our Members of Congress hear our voices and turn their attention towards the SMA Treatment Acceleration Act.

Health Staff have said emphatically that it is absolutely imperative that you – friends, family and researchers – set up time to see your Senators and Congressmen at their district offices during the August break. By arranging meetings, sending emails, and making phone calls, you are setting the stage for our Members to, without hesitation, sign on as cosponsors and support this legislation when health care reform is “out the door.” We want to be at the TOP of the list of priorities when the Members begin to focus on other issues at hand.

We cannot stress enough the importance of an aggressive grassroots effort over the August recess. It really is up to you, members of the SMA community, to make your voices heard and get your Members of Congress on board as cosponsors of the SMA Treatment Acceleration Act.

You are a mighty army, as evidenced by the enormous, unprecedented success of a single-disease bill in the 110th Congress. Let us continue our efforts, ten-fold! Let’s make the 111th Congress, OUR Congress!

As always, FightSMA is here as a resource for you. Should you have any questions or concerns, or would like help setting up meetings in your district offices, our phone lines (as well as email) are always open.

Please feel free to contact me at any time:
804-515-0080
carolinegibson@fightsma.com

Thank you all for everything that you do. We are continually inspired by your heart, dedication, and determination in fighting the good fight.

Warmly,
Caroline Gibson
Public Affairs Coordinator
FightSMA

Comments (0)
Categories : SMA Treatment Acceleration Act

New feature to raise awareness of SMA Treatment Acceleration Act

Posted: August 4th, 2009 | By: Staff | No Comments
Tuesday, August 4th, 2009

A new “Tweet This” button has been added to the Legislative Information page of the FightSMA website. By clicking the button, Twitter users can help get the word out to their followers about the SMA Treatment Acceleration Act by “tweeting” the following message:

I support the SMA Treatment Acceleration Act! Learn more about this important legislation here: http://bit.ly/ihyyl

The SMA Treatment Acceleration Act of 2009, introduced in the U.S. House of Representatives by Congressmen Patrick Kennedy (RI) and Eric Cantor (VA) and in the U.S. Senate by Senators Debbie Stabenow (MI) and Johnny Isakson (GA), provides federal support to complement the substantial private funding that is being invested to find a treatment for spinal muscular atrophy (SMA). Passage of this landmark legislation will enable scientific investigators to expedite national clinical trials and demonstrate that potential treatments are safe and effective for SMA patients.

Please “tweet” today!

Comments (0)
Categories : FightSMA News, SMA Treatment Acceleration Act

FightSMA receives grant from Newman’s Own Foundation

Posted: August 3rd, 2009 | By: Staff | No Comments
Monday, August 3rd, 2009

FightSMA is pleased to announce that the Newman’s Own Foundation has awarded the organization a $5,000 grant. Newman’s Own Foundation is a private, independent foundation established by Paul L. Newman. The Foundation continues the commitment of Paul to donate all net profits and royalties earned from the sale of Newman’s Own products to charity. As of June 2009, over $267 million has been donated to thousands of charities around the world.

FightSMA is a 501c3 non-profit organization headquartered in Richmond, Virginia. The organization is dedicated to finding a treatment or cure for Spinal Muscular Atrophy (SMA), the number one genetic killer of children under the age of two.

To see the announcement in the Richmond Times-Dispatch, click here.

Comments (0)
Categories : FightSMA News
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