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.