Myositis Empower Walk

DONATE NOW!

6TH ANNUAL MYOSITIS EMPOWER WALK OLYMPICS

Passing the Torch of Strength and Unity!

Event Date:

Saturday, October 19, 2024 – Virtual Format Only

Event Time:

1:00 pm PT/ 2:00 pm MT / 3:00 pm CT / 4:00 pm ET – Livestream Begins!

Location:

This year’s Myositis Empower Walk will be entirely virtual, but we’re bringing the Olympic spirit to you! Get ready for a gold-medal experience with plenty of exciting ways to engage with our sponsors and connect with the Landmans. While we won’t be gathering in person as in years past, we’re lighting the torch of celebration in a fun and fresh way—right in your own community. Stay tuned for more details on how you can participate and join in the spirit of unity and strength!

HOW TO GET INVOLVED

Donate

Give to support the work of Myositis Support and Understanding (MSU), an all-volunteer, patient-led nonprofit. You can dedicate your gift in memory or in honor of a loved one, and make it a recurring gift. Don’t discount the power of $5 and $10 donations! We can’t do it without YOU.

Donate Today

Create your fundraising team!

Create your Personal or Team Fundraiser and join the Olympic spirit! Rally your family and friends to be part of your winning team, and share it often to help raise the torch of support! Team fundraising is also about FUN-raising—compete in a Team Challenge and go for gold together!

CREATE A TEAM!

IN LOVING MEMORY, BOB LANDMAN

What is the Myositis Empower Walk?

The Landman Family created the Myositis Empower Walk in 2019 in loving memory of Bob Landman who passed away due to a too-late diagnosis of dermatomyositis. In 2020, the Empower Walk introduced the virtual experience, with live participation. There are no fees to attend. However, we encourage you to use this opportunity to invite your friends and family to get involved and help us fundraise. All money raised goes to Myositis Support and Understanding (MSU) and is used to further the mission, to improve the lives of and empower those fighting myositis. Learn more about Bob’s story by reading Our Dad was More Than His Dermatomyositis and watching LIVE with the Landman’s.