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Miles for Migraine Races and Youth Camps

 2 Mile Walk/5K/10K Run

Miles for Migraine is a registered 501(c)(3) Non-Profit with the mission of improving the lives of migraine patients and their families, raising public awareness about headache disorders, and helping find a cure for migraine. Miles for Migraine produces fun run events, typically 5k and 10k races to raise money for migraine research, and also hosts youth camps for kids and teens impacted by migraine or other headache disorders.

Phoenix

Time: March 18, 2017
6:00AM (5K Run)
8:00AM (5K & 10K Run)
8:30AM (2 Mile Walk)
Location: Mayo Clinic Phoenix Campus
5777 E Mayo Blvd, Phoenix, AZ 85054
Distance: 2 Mile Walk / 5K Run / 10k Run

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Washington DC

Time: October 15, 2017
7:45AM (5K Run)
8:00AM (10K Run & 2 Mile Walk)
Location: West Potomac Park, Washington, DC
Distance: 2 Mile Walk / 5K Run / 10k Run

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Philadelphia

Time: Saturday, October 8, 2016
8:30 am Start for all events
Location: Valley Green/Fairmount Park
120 W. North Western Avenue, Philadelphia, PA 19118
Distance: 2 Mile Walk / 5K Run / 10k Run

Chicago

Time: Monday, September 5, 2016
8:45 am
Location: Gerald Subaru Rooster 5K & Fling Mile at the 2016 Naperville Jaycees Last Fling
440 W. Aurora Avenue, Naperville, IL
Distance: 1 Mile / 5K Run
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San Francisco

Time: Sunday, July 31, 2016
7:45 am
Location: The San Francisco Marathon
Mission Street and The Embarcadero
Distance: 5K Walk/Run, HALF/FULL Marathon
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Virtual Race

Do you live in a city or town too far from one of our current walks/runs but want to participate anyway? Walk or run with us virtually! A virtual walk/race is one that can be done at any location. You can walk, use the treadmill, run outside or participate in another race in your town. You can walk/run your race at your pace wherever you like. You can fundraise first by collecting donations for yourself or your team, then register for our walk/run, and we will send you a goody bag with a t-shirt and finisher medal ($100 minimum donation necessary/goody bag).

Ending Social Stigma and Migraine

In addition to pain, sickness, and — for many — daily disability, migraine carries a severe burden of discrimination and negativity from many members of community.

This is social stigma.

 

History demonstrates that diseases that are stigmatized, like HIV, breast cancer, and autism, can only change in the public’s mind when the patients and their families come together in community action asking for recognition. Diseases in which the patients do not stand up for themselves remain badly stigmatized and patients do not receive the research or therapies needed to effectively treat their condition. This is true even if doctors speak up for the disease; patients and their families must take over the effort.

 

Patients with migraine often do not have the chance to stand up for their disease, and thus themselves. They desperately need an opportunity to do something positive about their condition. It is basic psychology that by collaborating positively with a group, you will feel better about yourself. Patients also need a way to encourage their families and friends to participate for migraine; doing something for someone else’s disease transforms attitudes and provides them an opportunity to learn about the scope of migraine.

 

Migraine is a major disease that receives about a 20th of the research dollars that should be given to it based upon its’ impact. Migraine patients desperately need new research to discover new treatments, and headache researchers and clinical specialists need to be trained. Miles for Migraine does all of these things; it does so by bringing patients together in community while also participating in an activity that is good for your health!

Miles for Migraine History

During a first-ever advocacy visit by the Alliance for Headache Disorders Advocacy to their respective members of Congress in September, 2007, a group of mostly M.D./PhD research and clinicians in migraine and headache disorders, including AHS member and migraine patient Eileen Jones, RN, PHN, were given a challenge.

Legislative Aides of Congress Persons and Senators told these research specialists that their quest for an increase in the National Institutes of Health spending allowance for headache research grants was flat (only ½ of 1% of the total budget), and would not increase in the foreseeable future. Furthermore, they were discouraged to hear that they needed to build public support in their home cities and states, where until the citizens start to demand funding, things would probably not change in their favor.  In response to this Congressional challenge, Eileen decided to start a competitive race.

Miles for Migraine held its first 5K and 10K run and 2-Mile walk in the fall of 2008 in San Francisco’s Golden Gate Park with approximately 200 participants. 

 

Our Vision

Our vision is to create some “big noise” in the community and raise the awareness of migraine and headache disorder as more than “just a headache”. We are planning to accomplish that by growing our signature event, the Miles for Migraine 5K, 10K and 2-Mile walk, and by implementing new programs such as a day camp for adolescents suffering from chronic migraines, and an adult seminar series.

 

Learn More

For more information and resources on Migraine and other headache disorders, visit our Migraine Information page.