4th Annual Myositis Empower Walk

4TH ANNUAL MYOSITIS EMPOWER WALK

Watch the Livestream

If you missed the 4th Annual Myositis Empower Walk, you can watch the livestream from YouTube or use the button below to watch on Facebook. This community-building event was held at the Discovery Park in Henderson, NV, on Saturday, October 8, 2022.

We are fundraising through the end of October!

Watch on Facebook

Make A donation

CREATE YOUR INDIVIDUAL OR TEAM FUNDRAISER

Let’s walk n’ roll to our biggest fundraising year yet!

There is still time! We are fundraising through the end of October!

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! Invite your family members and friends to be a part of it, and share it often to help raise funds! Team fundraising is also FUN-raising. You can even hold a Team challenge if you wish. We have how-to documents to make it easy!

Create your Team

When you watch the livestream, play Myositis Empower Walk

Bingo!

Click the button below to get your card.

Get your Bingo Card

Personal stories, fundraising tips & more

Read latest from the MEW blog

Making a Difference in the Myositis Community

Myositis Support2022-09-21T21:41:26-04:00September 21st, 2022|

This year’s walk, the 4th Annual, will be on Saturday, October 8th at Discovery Park in Henderson, and the Landman family would like to personally invite you, your family, and your friends to join them on this special day. Or, join from anywhere in the world via the interactive live stream.

Stephen Moore shares his personalized fundraising message

Myositis Support2022-09-06T09:52:41-04:00September 5th, 2022|

Stephen Moore, CME and Dermatomyositis Projects at MSU shares his fundraising message to give others a sense of how they might personalize their own 4th Annual Myositis Empower Walk campaigns.

Lynn Wilson, 2020 Mini Empower Walk

Jerry Williams2021-09-08T07:39:05-04:00June 30th, 2015|

Lynn Wilson, Vice President, MSU MSU Vice President and Director of Patient Centered Research, Lynn Wilson, joins LIVE on Facebook sharing her 2nd Annual Mini Myositis Empower Walk! Lynn Wilson shares her Mini Empower Walk

IN LOVING MEMORY, ROBERT “BOB” LANDMAN

What is the Myositis Empower Walk?

The Landman Family created the Myositis Empower Walk in 2019 in loving memory of Robert “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.