The second annual Walk of FAME will consist of hundreds of buddy-type walks in local communities nationally and worldwide. On or around May 12, teams of three or more—patients, family and friends wearing Walk of FAME T-shirts and equipped with information cards—will walk at an array of popular destinations.

Registration Fee: $35

Registration Packet: All registered participants will receive a Walk of FAME T-shirt, 10 information cards, a goody bag with an Awareness Day bracelet, and special offers, samples and literature from sponsors. (Registration packets will be mailed on April 24, 2009.)

Virtual Walkers: Those who are unable to participate in a community walk can still take part in the event by becoming a virtual walker.

Drawing: The names of every walker or virtual walker that registers for the Walk of FAME will be entered into a drawing, which will be held on Friday, May 15. For every 25 registered participates, the National Fibromyalgia Association will donate an online membership or an online subscription to Fibromyalgia AWARE magazine. (Details about our new online magazine will be announced in early April). The winners will be notified following the drawing and may choose to keep the selected item or give it to a family member or friend.

Awards: Four teams will be awarded a certificate and be recognized in Fibromyalgia AWARE magazine, following the event.

1. The team with the most walkers (individual participants)
2. The team that raises the most money (individual participants)
3. The team with the most walkers (business/organization)
4. The team that raises the most money (business/organization)

Registration may also be completed by mail:
National Fibromyalgia Association
2121 S. Towne Centre Place, Suite 300
Anaheim, CA 92806

Pledge Form: Download your pledge form HERE. Print it on an ink jet or laser printer using Adobe Acrobat Reader (free from Adobe if you don’t already have it).

Event Proceeds: Proceeds raised from the 2nd Annual Walk of FAME benefit the National Fibromyalgia Association, which develops and executes programs dedicated to improving the quality of life for people affected by fibromyalgia. The NFA focuses on patient support and education, awareness outreach, healthcare provider education, patient advocacy and the facilitation of scientific research.

Thank you to our sponsors

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