Kay’s Battle Against MS

Hello there ~ If you are taking the time to read my story, I appreciate you and all your support.

I never thought I would be writing a GoFundMe, at least not for myself, but I also never thought I would be diagnosed with Multiple Sclerosis at age 28.

The story begins in August 2022, when I suddenly lost vision in my left eye. I saw an optometrist who shared that this could be due to extreme stress. He used l words like “brain tumor” and “aneurysm” and recommended I go to the Emergency Room immediately.

As I paced the ER waiting room, I tried to think of all the different scenarios that could have landed me here. So many possibilities flooded my mind, but there was one outcome I had never considered.

After a spinal tap, MRIs, blood work and an overnight stay in the hospital, I was diagnosed with a life-long chronic illness- Multiple Sclerosis. My MRI revealed over a dozen brain and spinal cord lesions dating back to 2019.

For those not familiar with MS, here is a brief overview. The Central Nervous System attacks itself and creates symptoms ranging from fatigue, loss of vision, numbness, and trouble swallowing to loss of mobility and even permanent disability. Unfortunately, there is no cure for this debilitating disease, but there is a chance to stop the progression through disease-modifying treatments.

I am asking for your support to help me raise enough money to cover the handful of medical expenses I have incurred. Every little bit helps—even if you cannot donate, sharing this post would mean a lot.

Thank you for keeping me in your thoughts while I navigate this new life-long process. I am grateful for all your support.

With love,

Kayla