Myositis Empower Walk - #MyositisLIFE

2nd Annual Myositis Empower Walk, the Landman Family

3rd Annual Myositis Empower Walk!

Save the date of Saturday, October 2, 2021, for the 3rd Annual Myositis Empower Walk, live in Henderson, NV, and via interactive live stream worldwide!

More details are coming next week including fun activities building from last year’s virtual experience. This is our signature event, created by Lauren and Jenna Landan in loving memory of their father, Bob Landman, who passed due to dermatomyositis.

If you are interested in sponsoring the Myositis Empower Walk, contact Jerry Williams today!

NEW from the Myositis Empower Walk!

The 2nd Edition of the Myositis Empower Walk newsletter just launched!

Read 1st Edition here.

Read 2nd Edition here.

Myositis Empower Walk

The 2nd Annual Myositis Empower Walk was a huge success, raising over $18,000! It was held Saturday, September 19, 2020, in-person at Discovery Park in Henderson, NV, and virtually, LIVE on Facebook! If you missed it, no worries, you can watch the recording.

The Landman Family created the Myositis Empower Walk in loving memory of Robert “Bob” Landman. This year, the Empower Walk introduced the virtual experience, with live participation. We went LIVE on Facebook to Discovery Park with the Landman’s and Shelby, who enthusiastically hosted the LIVE video.

We look forward to the Third Annual Myositis Empower Walk in 2021. The date will be announced as soon as possible to allow you to plan!

Watch the 2nd Annual Myositis Empower Walk

Thank you for joining us Saturday, September 19, 2020, at the 2nd Annual Myositis Empower Walk, whether in-person at Discovery Park or LIVE on Facebook!

You made a difference. You brought the community together and we could feel the love and support. And it spread across the world with people joining us from the U.K., Italy, Mexico, Canada, and Australia.

The Landman family did a fantastic job. Our gratitude to Lauren and Jenna Landman for all of the work they do planning and promoting. And for Gladys and Chad Landman for their more behind-the-scenes work and support. Special thanks to Shelby for hosting the Facebook LIVE!

Thank you to all who donated, fundraised, and traveled to be at the walk. Thank you for your photos and videos so we can share them publicly.

Stay tuned for details about next year’s Empower Walk!

Robert ‘Bob”and Gladys Landman

About The Landman Family

When Robert “Bob” Landman became ill he was misdiagnosed several times. When he finally got the diagnosis of dermatomyositis, it was too late for any of the medications to be effective and Bob passed away due to complications.

Since, Gladys, Jenna, Lauren, and Chad have been involved to help MSU promote awareness and raise money to continue to further our mission.

What a great legacy Bob leaves for other patients continuing to fight this rare disease.

Read “Our Dad was More Than His Dermatomyositis” to learn more about Bob Landman.

If you have lost a loved one with myositis, share their information with us to be included in MSU’s Annual “A Day of Remembrance” video event. We want to publicly remember those we have lost.

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