My name is Laura Andreasen, and at the age of 58 my life changed forever. It began in April 2021 with a right foot drop, though months before that I had been experiencing frequent nighttime leg cramps.
I went to OrthoCarolina to have my ankle checked. The doctor ordered X-rays, an MRI, EMGs, and started me on physical therapy. When there was no improvement, I was referred to Dr. Story, a neurologist at Atrium Health. After an exam, blood work, and another EMG/NCS, he diagnosed me with Motor Neuron Disease (ALS). He encouraged me to seek a second opinion.
That took us to the Mayo Clinic in Jacksonville, FL. After another round of exams and EMG/NCS testing, I received the same diagnosis—this time described more specifically as a “slow motor disease,” primarily affecting my lower limbs.
My connection with ALS United North Carolina began during one of my early clinic visits with Dr. Story. Alicia Richardson from ALS United NC stopped by and shared information about the organization with my husband and me. Around the same time, a friend who already had a Walk ALS team in memory of his friend invited us to join. We combined efforts and formed “Warren & Laura’s ALStars.”
Since then, Brian Henry, Development Director at ALS United NC, has been wonderful in keeping me updated on Walk ALS and the campaign throughout the year.
I’d love for you to join me at Walk ALS Charlotte on November 1—or at one of the Walks in Greensboro or Wilmington this October. Together, we can raise awareness, fund research, and strengthen the support and services that so many ALS patients and families depend on here in North Carolina. Every step we take brings us closer to hope.