The folks here at Whedonopolis have gotten together and formed a team to walk in the Lupus Foundation of America’s Walk to End Lupus Now, which will take place on Saturday, September 26, 2015 in Exposition Park, Los Angeles, CA.
Why We Walk
Are you aware that Maurissa Tancharoen-Whedon, actress/singer and show runner/producer/writer for Marvel’s Agents of S.H.I.E.L.D. and all around sweet person, is living with lupus? We have all been entertained by her works and it is for her that we will be walking!
The Walk raises funds to support programs and services for people who are affected by lupus. Walk to End Lupus Now is the signature fundraising event of the LFA and is the largest Walk program dedicated to provide support to those living with the effects of lupus.
Our goal is to reach a total of at least $5,000 raised by the team. And you can help! Donate to our team now or, if the feeling moves you, join our team and walk with us!
Additional Incentives
In addition to the good vibes you will receive by donating to an important cause, Whedonopolis is putting together additional incentives to spark your participation. For every $100 you raise/donate, your name will entered in a drawing for great Whedon-related prizes! And your entries can build and build! Donate or raise $200 and receive 2 entries, $300= 3 entries, and so on. It’s that easy!
Be on the look out for more details about the drawing and join our mailing list (link next to our logo) to make sure you don’t miss a thing!
Even if you can’t participate or donate, please help spread the word about this very worthwhile event!
About The Lupus Foundation of America:
The Lupus Foundation of America is the only national force devoted to solving the mystery of lupus, one of the world’s cruelest. most unpredictable and devastating diseases, while giving caring support to those who suffer from its brutal impact. Their Mission is to improve the quality of life for all people affected by lupus through programs of research, education, support and advocacy. Find out more at www.lupus.org.
