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The SPSRF Staff
Jun 28, 20241 min read
Voices of SPS: Michael Weiss
Michael Weiss is a 19-year-old sophomore at the University of Michigan who was diagnosed with SPS at age 12 after a seven-month long hospita

The SPSRF Staff
Jun 28, 20241 min read
Voices of SPS: Angela Davis
Angela’s life began tragically. For years she suppressed emotional and physical pain. But after she was diagnosed with SPS, Angela became th

The SPSRF Staff
Jun 28, 20241 min read
Voices of SPS: Lea Jabre Fayad
Three things stand out immediately about Lea’s story. First, she has scoured the world to find a diagnosis and treatment.


The SPSRF Staff
May 15, 20242 min read
Voices of SPS: Chelsea L.
I feel like I’m not living a lie anymore. I feel I’m not second-guessing anymore. I also feel like I want go to all the neurologists that ha


The SPSRF Staff
May 15, 20242 min read
Voices of SPS: David Axelrod
My name is David Axelrod. I reside in Milford, Connecticut, and work as a Senior Talent Acquisition Specialist. But to truly know me, you ne


The SPSRF Staff
May 15, 20242 min read
Voices of SPS: Ann Thompson
Hello, my name is Ann Thompson. I was diagnosed with Stiff Person Syndrome (SPS) at the age of 73 after spending a grueling 15 months searc


The SPSRF Staff
May 15, 20242 min read
Voices of SPS: Rachel Hallstrom
My name is Rachel Hallstrom, and I'm a college student in Anchorage, Alaska. At eighteen, I was a picture of health, training for a triathlo
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