About Me

  • Gender Female
  • Age 19
  • Relationship Single

My Story 1 Appreciate this

I was diagnosed with MS mid-September of 2018 a week before my 18th birthday and during my exchange year in Munich, Germany. I was awakened my overall numbness in my legs and back and had no idea why it had occurred, but I thought it would only be temporary. It hurt to walk and do my normal activities. I finally went go a doctor and they referred me to a neurologist, who told me that my neurological activity was not functioning as it should be. After an MRI scan the doctors noticed big lesions in my brain and my mid-torso, which was a big explanation. A few other tests later, it was clear to the doctors that I had MS. I was then hospitalized for 5 days and received a Cortisone infusion which relieved the numbness. My father also has MS and struggles with it every day. My biggest challenges are dealing with the fatigue and feeling like I can't perform normally. As a child, I also had major MS attacks, such as the time when I was 13 when I fell down and had no memory of it happening, almost as if I had fainted. My Hopes are that I will have a chance in my adult life to live normally and wonderfully, and to find a medication that would make that possible. My best piece of advice to those newly diagnosed, as someone newly diagnosed myself, is to always keep a positive mindset. Don't let it become a major obstacle in your overall path to happiness and find joy in things you want to do. Positivity is your biggest best friend.


Living Well with MS Emotional support, Healthy living
Getting Involved Advocacy
Hobbies and other interestsCrafts, Medicine, and overall health

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