The Oronuga family’s life was turned upside down when Teniola was diagnosed with MG at age three. They share what it is like to battle this chronic autoimmune condition in Nigeria.

An MG diagnosis leads to a passion for raising awareness and giving back.

Raising awareness and racing for a cure with a one-of-a-kind fundraiser.

This is not a weight loss journey.

Learn more about a key member of our volunteer Board of Directors.

It's more important than ever to restart the MG Walk. We’re closer than ever to a world without MG. But to get there, we need you. 

“We want to find a way to give back to an organization that’s been tremendously helpful to us.” 

Read an excerpt from this new ebook, full of humorous and honest tales about life with myasthenia gravis.

Sarah Wright, DO MS, joined us on March 20 to discuss a hot topic in the MG Community

Here I was in my early twenties, my work was getting known all over the world, but I was secretly battling a potentially life-threatening disease