On February 2,2018 I was diagnosed with MS short for Multiple Sclerosis. After 8 yrs with 5 different doctors all afraid to diagnose, my condition worsened. After 8 long years of battling so many unpredictable symptoms in and out of the hospital not being able to work, not being able to spend time with my children I was finally diagnosed with Multiple Sclerosis (MS).

I say finally as 5 different doctors here in Vegas told me “wow everything looks like MS but i can’t diagnose you, let me send you to this doctor”. That cycled continued for 8 yrs. within that 8 yr period i was told to go to one MS specialist but unfortunately she didn’t take my insurance.

I would’ve had to deal with surprise billing and I couldn’t afford that so the search continued symptoms began to progress until i landed in the hospital with no sensation in my legs and complete no left side feeling. After spending several weeks and months in the hospital time taken away from my kids I decided it’s time to fight back!

How can i make a change that no one else will have to go through what i went through. How can we provide funding for more doctors to learn and diagnose people like me?! So i researched i said i will not let MS have me. How can i take control of this fight?! Help me change the world forever!

I’ve created a hashtag #ms🎗me meaning: MadeStrong = (MS) = 🎗(& )  ME = (my journey)

Email: MADESTRONGATHLETICS@GMAIL.COM Instagram: Madestrong_athletics   I have become an advocate for the National Multiple Sclerosis Society, and donations will be sent for research.