International Trigeminal Neuralgia Awareness Day October 7th!
5,071 Comments
O
Ola Aylwin
9 years ago
Dear WHO: Please add Trigeminal Neuralgia to your Health Topics List. As a sufferer, I agree it is very important to create awareness and access to funding and research for this terrible disorder. My pain never stops.
A
Andrea Brown
9 years ago
I have a friend who suffers from this.
A
Anonymous
9 years ago
There is no cure
P
Patricia Garner
9 years ago
I'm newly diagnosed!☹️
R
Russell D King
9 years ago
I know some one who has it I cant even imagin the pain she suffers.
A
Anonymous
9 years ago
Trigeminal neuralgia sucks
R
Robyn Hodgson
9 years ago
Had ATN now for 4 years I don't go a day without pain.
C
Cheryl Parrott
9 years ago
Please work to find a cure and medication for this awful disorder.
A
Andrea Gentry
9 years ago
It is of VITAL importance that WE- the people living with this horrendous pain, be validated in the form of WHO taking action..
D
Donna Brodt
9 years ago
For all those suffering and to make this awareness world wide!
S
Simon Roberts
9 years ago
My wife struck down with this awful painfully dibilitating condition to which vastly more money & research should be de
J
Joann
9 years ago
My daughter is suffering from this horrific condition, it took along time to diagnosis because of ignorance. Please spread awareness with this special day.
B
Betty Latuso
9 years ago
Heart breaking to see someone in so much pain!!
K
Katherine Scopel
9 years ago
I've had TN for 6 years. We need help! We need a cute! We need relief!
A
Anonymous
9 years ago
I have MS related TN.
C
Cindi Drummond
9 years ago
Trigeminal Neuralgia needs funding and research. Please do the right thing!
F
Frederick Sison
9 years ago
Hope to grant this so WHO get to know those are suffering with this kind of desease.
God bless
K
Kathy R Hall
9 years ago
I have this dreaded TN!
A
Anonymous
9 years ago
TN sufferers need to have people understand the disease, suffering, and frustrations they endure. Health professionals especially need to be aware do the patients can be clearly and correctly diagnosed.
D
Danielle Collins
9 years ago
I have TN. The doctors where I live has no idea and aren't willing to help because the don't anything about TN.
Dear WHO: Please add Trigeminal Neuralgia to your Health Topics List. As a sufferer, I agree it is very important to create awareness and access to funding and research for this terrible disorder. My pain never stops.
I have a friend who suffers from this.
There is no cure
I'm newly diagnosed!☹️
I know some one who has it I cant even imagin the pain she suffers.
Trigeminal neuralgia sucks
Had ATN now for 4 years I don't go a day without pain.
Please work to find a cure and medication for this awful disorder.
It is of VITAL importance that WE- the people living with this horrendous pain, be validated in the form of WHO taking action..
For all those suffering and to make this awareness world wide!
My wife struck down with this awful painfully dibilitating condition to which vastly more money & research should be de
My daughter is suffering from this horrific condition, it took along time to diagnosis because of ignorance. Please spread awareness with this special day.
Heart breaking to see someone in so much pain!!
I've had TN for 6 years. We need help! We need a cute! We need relief!
I have MS related TN.
Trigeminal Neuralgia needs funding and research. Please do the right thing!
Hope to grant this so WHO get to know those are suffering with this kind of desease. God bless
I have this dreaded TN!
TN sufferers need to have people understand the disease, suffering, and frustrations they endure. Health professionals especially need to be aware do the patients can be clearly and correctly diagnosed.
I have TN. The doctors where I live has no idea and aren't willing to help because the don't anything about TN.