Natasha Acoff is the founder and president of On My Nerves, Inc., a nonprofit organization dedicated to supporting individuals affected by Multiple Sclerosis (MS) through advocacy, education, community outreach, and fundraising. Diagnosed with MS in 2014, Natasha has transformed her personal journey into a mission to create a more informed, supported, and empowered MS community in Tallahassee and the Big Bend region.
As a National Multiple Sclerosis Society Ambassador, Natasha leads efforts to raise awareness and connect individuals with critical resources. She serves as the leader of the local MS Self-Help Group and the Community Engagement Council, providing support and guidance to those navigating life with MS. She is also an active participant in MS Public Policy Conferences, Proclamation Acceptances, and Advocacy Storytelling, working alongside legislators to improve healthcare access and policies for the MS community.
In addition to advocacy, Natasha plays a key role in fundraising and community engagement. She is a Walk MS Captain and Champion, organizing events that bring people together while raising essential funds for MS research and support services. She also serves on the committee for the Annual Tallahassee Together For a Cure Luncheon, furthering efforts to drive awareness and funding.
Beyond her nonprofit work, Natasha is a full-time mother, STEM advocate, and an IT professional with over 17 years of experience. She is deeply involved in supporting STEM education programs, school enrichment activities, and initiatives that inspire young learners.
Her dedication and impact have earned her numerous accolades, including the 2024 Resilience Domi Award and the 2024 Florida State University School of Information Distinguished Alumni Award, recognizing her contributions to society and the MS community.
Through On My Nerves, Inc., Natasha remains committed to building a stronger, more connected MS community—one where individuals feel empowered, supported, and never alone on their journey.
Here's a quick history lesson (year after year) on my MS journey. Note: I'm pulling a lot of things together as they relate neurologically. Check out my blog in the NEWS section for more.
1992 - Tallahassee, FL
First memory of migraine/nausea
1999 - Tallahassee, FL
Multiple Neurology visits. MRIs. Nerve tests. - No Diagnosis
2011 February - Baton Rouge, LA
I had Bells Palsy. You all remember that partial facial paralysis. #screwface #twoface
No Diagnosis
Treatment - Steroids and Speech Therapy
2014 April - Trenton, NJ
First, notable, flair. Numbness on the left side of my upper body.
Diagnosis - Multiple Sclerosis
Treatment - Hospitalized steroids #FallRisk
2016 April - Trenton, NJ
Small flair. numbness of my foot.
Treatment - Outpatient steroids
2019 April - Tallahassee, FL
Second, notable flair - Numbness/Loss of sensation chest (includes arms) to feet. And limited mobility in hands (there's a video for that)
Treatment - Hospitalized steroids. #WorstFlairEver
Here we are today, my legs (from what i feel) has regained that loss of sensation. My arms have regained strength. I'm doing exercises that I got from OT and PT to conquer the stiffness, weakness, etc. I'm just percolating on! #FeetDontFailMeNow
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