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Support Group: Parents Monthly Support Group

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Support Group Telecon

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On this day, July 26, 1990, the Americans with Dis

On this day, July 26, 1990, the Americans with Disabilities Act was signed into law. Today we celebrate its 34th anniversary.💚

While we still have a long way to go, today is day to reflect on all of those who have fought for the fair treatment of disabilities throughout history—and the progress that has been made so far.

#myNMOfamily #theGJCF #love #hope #community #family #dogood #nonprofit #NMO #NMOSD #raredisease #activism #advocacy #science #research #patientadvocacy

Mantén tu rostro siempre hacia la luz del sol, y

Mantén tu rostro siempre hacia la luz del sol, y las sombras caerán detrás de ti."

"Keep your face always toward the sunshine, and shadows will fall behind you."

#myNMOfamily #theGJCF #love #hope #community #family #dogood #nonprofit #NMO #NMOSD #raredisease #activism #advocacy #science #research #patientadvocacy

What is something you practice for a successful do

What is something you practice for a successful doctor’s appointment?🩵

Comment below!

#myNMOfamily #theGJCF #love #hope #community #family #dogood #nonprofit #NMO #NMOSD #raredisease #activism #advocacy #science #research #patientadvocacy

“Not only did I learn things, be reminded of thi

“Not only did I learn things, be reminded of things, but it also reminded me in a different way how similar experiences can be and how resilience is needed and how it shows up…it might be a different fruit but it’s still fruit.” - Monica Lewinsky on listening to Guthy-Jackson’s patient panel

Still thinking about the amazing discussion between Founder Victoria Jackson and guest speaker Monica Lewinsky at our Los Angeles Patient Day. It was a remarkable day to talk about resilience!💚

#myNMOfamily #theGJCF #love #hope #community #family #dogood #nonprofit #NMO #NMOSD #raredisease #activism #advocacy #science #research #patientadvocacy

“No cuentes los días, haz que los días cuenten

“No cuentes los días, haz que los días cuenten.” – Muhammad Ali

“Don’t count the days, make the days count.”

Regístrate aquí para el grupo de apoyo de habla hispana: https://us02web.zoom.us/meeting/register/tZAvfuGpqjwqGtGwIWOE5GvVkjTEQ6L5ClDV?fbclid=IwAR1nUlpiUSlXPdF4GHIJMPK0Eqc8P23bTaecHA-HPw1OfLyhlKWngiCkl40#/registration

#myNMOfamily #theGJCF #love #hope #community #family #dogood #nonprofit #NMO #NMOSD #raredisease #activism #advocacy #science #research #patientadvocacy

It's OPEN! Register now for our Together - Oklahom

It's OPEN! Register now for our Together - Oklahoma City NMO Patient Education Day event! Connect with the NMO community and learn from leading neurologists!💚

Register at the link in our bio!

What is a goal you have for yourself this summer?🧡

Comment below!

#myNMOfamily #theGJCF #love #hope #community #family #dogood #nonprofit #NMO #NMOSD #raredisease #activism #advocacy #science #research #patientadvocacy

Time doesn't take away from friendship, nor does s

Time doesn't take away from friendship, nor does separation.”

From far and wide, our rare community forms bonds that stands the test of time and distance.💚

#myNMOfamily #theGJCF #love #hope #community #family #dogood #nonprofit #NMO #NMOSD #raredisease #activism #advocacy #science #research #patientadvocacy

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