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 made it their mission to promote awareness and help MSU raise money to continue the important work we are doing for those like Bob who needed a quick and accurate diagnosis for a chance at life with dermatomyositis.
Bob leaves a great legacy for other patients continuing to fight this rare disease.
The 2nd Annual Myositis Empower Walk was a huge success! It was held Saturday, September 19, 2020, in-person and virtually! If you missed it, no worries, you can watch the recording. Visit the Myositis Empower Walk page at https://understandingmyositis.org/empowerwalk/ for more.
Mail checks payable to MSU to 9125 N. Old State Road, Lincoln, DE 19960. Add "Empower Walk 2020" in the memo field or include a note. Donations are tax-deductible in the U.S. and are used to further the mission and patient-centered programs of Myositis Support and Understanding (MSU). Thank you for your support!