Our Founder
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.
My MS/Neuro Story
This Quick and Dirty
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.
Here's a little story, all about how...
I've had a history of migraines. I can remember back to 2012 when I had one so bad, I vomited. Gross? Of course not, that's natural. I've been seeing a neurologist since I was at least 19. No, I'm not crazy. Even then I'd reported nerve related symptoms so I'll say, I probably should have been diagnosed before then 2014. But maybe not. Maybe the timing was just right.
2011 February
I had Bells Palsy. You all remember that partial facial paralysis moment? #screwface #twoface Listen, waking up to a numb face is not my idea of a good time. Thankfully my PCP got me started, immediately, on running test, seeing a neurologist and starting speech therapy. My Neurologist, at the time, noted the potential of optic neuritis (symptom of MS).
2014 April
I had my first, notable, flare that led to the diagnosis of Multiple Sclerosis. Numbness on the left side of my upper body on Easter Day. I'd gone to Urgent Care but they didn't have any way to really 'check' me. I traveled back to NJ the next day, feeling uneasy because the numbness had progressed. So, instead of going to work, I went to the hospital. They took me in immediately, began running tests and before I left that evening, I was 99% sure I had Multiple Sclerosis. A few weeks later, I had an appointment with a new Neurologist. He stated that based on my MRI I wasn't going home and instead I was being admitted to the hospital to begin a steroid treatment. Things begin to feel better shortly thereafter.
2016 April
I had a small flare, numbness of my foot. By this time I was seeing an MS specialist. There facility allowed me to come in, do a quick steroid treatment (outpatient) and I felt better.
2016 November
I'm Pregnant. So, I have to stop my medication. They say, pregnant women have less symptoms when they're pregnant but may relapse, harder, post partum. July 2017, I had a healthy baby boy and began treatment again in December 2017.
2019 April
I cam home for the MS Walk and was preparing to head back to Puerto Rico, for work. But, I began feeling numbness around my midsection and legs so I went to the Emergency Room. I wanted to be sure before I go to PR and had to be admitted. They treated me for Potassium and Magnesium. Oh yeah, and I'm pregnant again! As days progressed, so did the numbness. So that theory that women don't have symptoms during pregnancy went right out the window. I was hospitalized for 7 days, doing a steroid treatment with a most uncertain recovery. A few days in, I woke with limited mobility and function in my arms and hands. Stiffness, numbness and weakness hand taken over. I hadn't gotten better, I'd gotten worse.
I came home and began my recovery. Over time, my legs had regained that loss of sensation. My arms still had some weakness. My hands were still numb. I started doing exercises with OT and PT to conquer the stiffness. Ultimately, I made a full recovery with some small moments of weakness.
2020 January
Numbness is a thing. It's not fun, but it's a thing. Once again, post baby and not being back on meds yet, I'm having a flare. It wasn't BAD but significant enough that I needed to do another treatment. The difference, COVID diagnosis are coming in. The emergency room was packed. I waited almost 9 hours in the ER before I got a room to start my treatment.
2021 on with a few random flares here and there... but I'm still standing!
Just percolating on! #FeetDontFailMeNow