We’re asking US citizens to participate in this event. Change for all cluster headache patients, worldwide, is our motivation! In 2012, twelve cluster headache patient/support persons joined our DC Advocacy team. Let’s double that number in 2013!
The following link has all the details and registration information for this year’s trip to Washington DC.
CLUSTER HEADACHE SUFFERERS,
JOIN US IN WASHINGTON, D.C.
Making Our Voices Heard in D.C.
We NEED more cluster headache research and more effective medical treatments! Clusterbusters will be returning to Washington with The Alliance for Headache Disorders Advocacy for our second year to meet with congressional leaders on April 8-9, 2013. Together we will push for senate hearings on the need for increased funding for headache research.
Three Ways That YOU Can Make a Difference!
1. JOIN OUR ADVOCACY TEAM IN WASHINGTON
Make YOUR voice heard! We need people from as many states as possible to join us in D.C.. Do you think we need more reasearch and better treatment options for cluster headaches? We are inviting people with a with a story to tell and a passion for making a difference in the lives of cluster headache sufferers to join us in D.C..
Hurry! Deadline to register to participate in “Headache on the Hill” is March 8th, 2013! This is to allow ample time to schedule appointments with congressmen and senators.
The Alliance for Headache Disorders Advocacy is offering one night of FREE lodging per participant. In addition, a limited number of partial travel scholarships for the “Headache on the Hill” event are being made available to specifically get a cluster headache patient or support persons “voice” on the team to D.C.!
2. WRITE TO YOUR REPRESENTATIVES
Watch for our event updates to participate in the “Advocacy Letter” campaign. We urge everyone to participate! . Our goal is to send a strong message to all representatives, nationwide. We hope to flood the capital with thousands of on-time letters supporting “Headache on the Hill”!
3. SEND A DONATION
Your tax deductible donations are not only appreciated, but essential to our continuous research, education and advocacy efforts. Clusterbusters works hard to advocate on behalf of ALL cluster headache sufferers – regardless of their method of treatment. Thank you for supporting our efforts!
After receipt of your information, our Advocacy Team will email you additional trip details. Remember, there are 2 registration forms. One with Clusterbusters AND with The Alliance. We look forward to another great trip with you!
Questions? Email us at firstname.lastname@example.org