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They’ve Been Walking for 20 Years
Lora Lacey was in her senior year of high school when she suffered a viral infection that affected her muscles. At the time, her mitochondrial disease was barely noticeable and she would not get an official diagnosis of mitochondrial myopathy until she was 19.
Chance Meeting Leads Patient To First Symposium
An online search for Kearns-Sayre Syndrome (KSS) led Rachel Godshall to attend the UMDF’s annual Symposium.
Donors Make History for accelerators Project
Project donors helped our community make history after the Big Pitch event at Mitochondrial Medicine 2019.