Registration Open for 8th Annual ‘Walk With The Stars’ Event
Registration is open for the 8th annual “Walk with the Stars,” one of the largest fundraisers organized by the Sickle Cell Disease Association of America (SCDAA) that supports the development of better treatments and a cure for sickle cell disease (SCD).
All proceeds from the July 10 event will go to SCDAA programs that are aimed at preventing disease complications through education, advocacy, increased awareness, and research. The two-hour fundraiser kicks off at 9 a.m. ET. Registration is $10.
The event is virtual again this year, so participants may walk, run, dance, jump rope, or even Hula-Hoop, at home or wherever they are to support the nonprofit organization. The top fund-raising teams and individuals will receive prizes.
The annual walk brings together advocates of every stripe and background across the U.S. to raise funds, as well as awareness. To date, the event has raised more than $500,000 to improve treatments and the quality of life of members of the sickle cell community. The goal for this year is to raise $30,000.
“When you participate in the Walk with the Stars, you are helping to build a future where there is a universal cure for sickle cell,” the organization stated in its announcement. “Together we are stronger. Together we can break the sickle cycle.”
Although event participants are welcome to raise funds through sponsorships of individual walks and runs in local communities, the organization also is encouraging the formation of virtual teams. More information on sponsorship opportunities is available here.
“Walk with the Stars is the perfect opportunity to encourage friends, loved ones, and coworkers to make a life-impacting change for all those affected by sickle cell disease,” the SCDAA stated. “United with every walker and runner, together we can raise the necessary funds which will get us that much closer to finding a universal cure.”
The event is being tagged and shared on social media with the hashtag #MoveForSickleCell.
Established in 1971, the SCDAA advocates for those living with SCD, and seeks to empower community-based organizations to maximize patients’ quality of life, while advancing the search for a cure.