The Myositis Empower Walk was created by the Landman Family in memory of Robert “Bob” Landman who passed due to dermatomyositis.
Here you will find Bob’s daughters, Lauren and Jenna Landman, writing articles, sharing empowering stories, and keeping us updated about all things Myositis Empower Walk.
If you are interested in speaking with Jenna and Lauren about sharing your Empower Walk story, email them at empowerwalk at understandingmyositis.org
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Clinically Amyopathic Dermatomyositis
Inclusion Body Myositis
Necrotizing Autoimmune Myopathy
Other (not listed)
Introducing the Myositis Empower Walk Newsletter (MEWN)! Meet Angela, Holly, and Ashley!
Our dad's time with dermatomyositis was only a small portion of his life, although a very monumental time in our life.