Resources For the Blind

Many with MOG-AD, despite the efforts of their medical professionals find themselves with permanent damage to their optic nerves and therefore have low or no vision in one or more eyes.  With improved testing and diagnosis, our hope is that no person loses their eyesight.  Until then, we are proud to provide resources for our Blind MOG-AD patients.

For those who need help finding ways to adjust to a new way of living, our Director of Blind Advocacy, Andrea Mitchell is working to provide information and tips for helping those in need.  Having her life changed by MOG-AD, she has learned many new things in order to regain her independence, and is passionate about helping others who find themselves blinded by this disease.

Our MOG Dog, Newcastle, Caregiver for Andrea Mitchell

Our MOG Dog, Newcastle, Caregiver for Andrea Mitchell

Newcastle, The MOG Project Mascot & Guide Dog

Useful links

Below is a summary of the resources used in Breaking Through the Darkness by Andrea Mitchell.  Some are particular to the greater San Francisco area, but many are in the US nationwide, or are useful to anyone in general, worldwide. There are a lot of other resources out there depending on location. We are in the process of gathering and publishing resources from around the world.

UK Resources

This list was compiled by our UK Outreach MOG Squad member, Sarah-Huson Whyte:

From our Partners

Our partner, the Siegel Rare Neuroimmune Association, held the 2020 RNDS Symposium and offered this talk on How to Manage Visual Issues.

Articles that you may find useful

Resources For The Blind

My Guiding Angel Eyes

A Story About Newcastle, His Extraordinary Abilities, And Our Partnership My name is Andrea, and I have lost most of my sight in both eyes due to a rare orphan…
Resources For The Blind

Breaking Through The Darkness

My name is Andrea, and I was officially diagnosed with MOG antibody disease (MOGAD) in 2013. At that time, there was not much known about the disease. The first two…