Jacqui Atkinson endured six years struggling to understand the paralyzing muscle spasms and chronic pain taking over her body.
Through countless visits to doctors, many of whom accused her of feigning her severe, days-long spasms, she held onto hope and faith until she found the answer: Stiff Person Syndrome.
She chronicled her journey in her memoir, One in a Million, and to help raise awareness of the condition is generously donating 50% of book sales to The SPSRF. Get your copy here.
If you have any questions or comments about your experience, please share them with us using the short form below, and a member of The SPSRF team will reach out to you.