From one rare mom to another...Victoria Jackson, you are a super hero. This foundation that you and Bill built, is a world changer. Thank you for letting Behind the Mystery tell this story with you.
@christyabercrombie39168 ай бұрын
As a patient with NMO, it's so wonderful to see so much attention being given to this disease. It was a lonely place in 2012 until I found my NMO family and The Guthyjacksonfoundation!!! 💚💚💚
@mollyheywood2778 ай бұрын
What powerful NMO stories!
@MK-oc6jx8 ай бұрын
God bless you God be with everyone who has an M all my sister-in-law is fighting it right now for the last year and it’s a horrible disease. I’m so grateful you have this to give us more insight on different options and places to go and how to tell the doctors.
@lindasilva08275 ай бұрын
My middle child 2 months before his 30th birthday, wake up paralized, been to 6 different hospitals, and no doctors can find what is wrong. All this makes sense. Do I need a neuro? What kind of specialist