Some of the ways you can help cluster headache patients and spread awareness about the severity of this disease include:
Clusterbusters has an annual patient conference every September and a virtual #CureforCluster 5k event each summer to bring people together and share information. We partner with other nonprofit organizations that have activities such as Miles4Migraine and the Coalition for Headache and Migraine Patients (CHAMP). Learn more on our Events page.
We have several regional support groups set up across the United States and some international meetings as well. These are small, intimate gatherings that allow clusterheads and their loved ones to meet others who are going through the same struggles as well as share and learn more about treatments and advocacy. The frequency of the meetings vary from every month to quarterly and largely depend on the availability of attendees. Learn more about established groups or starting one in your area on our Regional Groups page.
Advocacy for Cluster Headaches
Advocacy takes on many forms, from being your own advocate at doctor’s appointments and pharmacies to joining others online and in-person to raise awareness and change public health policies. Becoming an advocate can be a powerful experience and help you go from “suffering” with cluster headaches to overcoming and fighting back against the attacks. This can be done on social media, at events such as Headache on the Hill, participating in our #CureforCluster 5k, or volunteering at Clusterbusters. Learn more on our Advocacy page and check out our Volunteer Opportunities.
Signing up on our patient registry is another way you can get involved in the research and awareness of cluster headaches. The straightforward questionnaire allows you to join thousands of other patients who have signed up to help further our understanding of the condition. Learn more on our Patient Registry sign-up page.
A simple way to help further the mission of Clusterbusters in advancing research, advocacy, and awareness of cluster headaches is to donate to our nonprofit. These funds are used in several ways ranging from direct-to-research donations to scholarships for clusterheads to attend events such as our conference and Headache on the Hill to administrative costs that help us continue our work. You can do a one-time donation or sign-up for a recurring donation. Learn more on our Donate page.
These are a few of many options available to get involved with Clusterbusters and helping cluster headache patients. If you have questions or an idea for advocacy, contact us, and check out our forums to connect with others.