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My Life with JDM

Juvenile Dermatomyositis

A couple of months ago I decided to start a blog that follows my life with my disabilities. I am the proud reciepient of Juvenile Dermatomyositis and Fibromyalgia. My life is far from perfect and I'm always trying to find the brighter side of things and keep going. JDM is very rare so I look to provide awareness as often as I can. And everything else I have is secondary to the JDM. There's a little list of mental things that go along with it all. So please feel free to read my story on www.mandi-saturday.com Or follow my Instagram or even find me here. -Mandi 🎈

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Blogger of Disability: www.mandi-saturday.com Facebook, Instagram, Snapchat Diagnosed in 1997 Reborn 2010 Now I'm just sharing my story for awareness. Not all disabilities are visible. Trying to cure my Insomnia. #cureJDM 🎈

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Mandi Presley

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My Life with JDM

A couple of months ago I decided to start a blog that follows my life with my disabilities.
I am the proud reciepient of Juvenile Dermatomy