Who is Maggie Slighte?

Maggie Slighte was born and raised and raised 3 children in Western Washington. Her early adulthood was spent first in the medical field and then as a computer programmer. Having been told there was “no money in writing,” her dreams bled into journals while she raised her family and worked for the State of Washington.

Maggie surprised her friends and family in 2013 by following a still, small voice in her heart to the The Church of Jesus Christ of Latter-Day Saints. The shock was on the other side when she abruptly left the Mormon church in September 2021, removing her records in January 2022.

Maggie finished her Bachelor’s Degree in Nonfiction writing at Southern New Hampshire University in August 2017. Since graduation, she has studied post-graduate work in the field of Creative Nonfiction at two Universities.

After exposure to an antibiotic (levofloxacin) in mid-2017, Maggie’s disabilities profoundly increased. While her stature is different in a powerchair, she has found a new opportunity for her spirit of advocacy while traveling over broken sidewalks.

The fluoroquinolone toxicity uncovered the fact that Maggie was born with a congenital condition. Following her antibiotic injury, she was diagnosed with Ehlers-Danlos Syndrome in 2019. Maggie was 53 years old when she learned she was born with the congenital connective tissue disorder.

The diagnosis was cathartic. Maggie has made is one of her life’s missions to bring awareness about Ehlers-Danlos Syndrome to the world

In 2021, Maggie entered a new phase of her life by opening a TikTok account to increase her audience of advocacy. After her first viral video in August, TikTok became her primary social media with an audience of nearly 20k followers.

When she isn’t writing, advocating, or traveling, Maggie enjoys spending time with her grandchildren and her two dogs and her caregivers.