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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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