About Me

  • Gender Female
  • Age 51
  • Relationship Married

My Story 0 Appreciate this

I was diagnosed with MS after an MRI and LP in early fall of 2001 when my son was 10 months old. Looking back we realized I had symptoms that were missed by MD's for about 4-5 years. It doesn't help to look back at and be mad, frustrated or any other negative emotion I experienced. Life happens and Medicine is not perfect. I know I should thank God more often than I do for those who have worked to find a cure for MS, and other diseases. I am thankful that I am now taking a pill daily with no side effects that is a disease modifying drug for M.S. My biggest challenge is walking without tripping or falling from an outward appearance, and pacing myself. Another challenge is having my kids understand that my pace is different then theirs and that it's okay. My hope and dream is to be a part of my husband and children's lives as long as God allows which with my genes should be another 40-50 years. What I tell to people newly diagnosed or family or friends of someone? " I've had MS for more than 15 years and it doesn't have me. I'm thankful that I am the only family member ever diagnosed with this disease and I'd rather it be me than any of my large extended family. Do not believe


Type of MS Relapsing-Remitting MS (RRMS)
First experienced symptoms1997
First Diagnosed 2013
Symptoms Numbness, Walking (Gait), Balance, & Coordination Problems, Emotional Changes, Spasticity
Treatments Ampyra, Avonex, Corticosteroids (SoluMedrol, Deltasone), Exercise, Gilenya, Tysabri, Vitamin D, Only on Gilenya and Ampyra now

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