International Trigeminal Neuralgia Awareness Day October 7th!
5,071 Comments
W
William Sweeney
12 years ago
We need this done asap
G
Greg Masters
12 years ago
TN SUFFERER , we need a CURE
R
Robert Coveno
12 years ago
For Wendy...
N
Naomi di Gavriel Gertner
12 years ago
Ladies and Gentlemen of WHO,
Recognition and faster remedy for TN sufferers is PARAMOUNT.
Not helping is equal to condemning these patients to life in a torture chamber....which is a Primal Fear of everyone on Earth.
Please add Trigeminal Neuralgia to the Health Topics list. It is about being humane and civilized.
Respectfully,
Naomi di Gavriel Gertner
A
Albert pena
12 years ago
Supporting the ones I love
A
Anonymous
12 years ago
I am supporting LeeLeeBot who suffers from this terrible condition.
L
Lianne Keiller
12 years ago
This disease is slowly, but surely, taking whatever quality of life I had away. Praying for relief.
A
Andrea Mearls
12 years ago
Please find cause and cure.
J
JP Bosman
12 years ago
I have a colleague who is suffering from this condition. Please find a way for TN to be cured.
P
pamela doyle
12 years ago
Unbelievable that something like this can exist. Horrible. Hope they find a cure!!!!!
A
Anonymous
12 years ago
Please help stop the pain.
S
Susan Ranstead
12 years ago
Please help raise awareness, help with research funding, help us get our lives back.
P
Patrick Steele
12 years ago
7 yrs now and 2 surgeries later. Still on Meds and told there isn't really anything they can do at this point because there just isn't alot of research out there to know how to fix it.
M
Mary Dinet-Phillips
12 years ago
This is for you JEN!
H
Heather Smith
12 years ago
I have bilateral TN1 &TN2
H
Helen Cowan
12 years ago
For TN sufferers the process of referral to treatment takes longer than it should... from onset to treatment is not much better either!! This is accross all nations, we wait longer, in agony, which results in suicide. There is no let up either we are in pain or feel like zombies. We take antiepilespy medication, the best bet there is, but still we get pain as we have no specific medication for our condition
Please help us!!
B
betty webb
12 years ago
hope is our only hope
A
Alli McCarthy
12 years ago
HELP US FIND A CURE!!! I have TN on the right side of my face
and it affects all branches.
E
Elizabeth Hurley
12 years ago
Let's get this on everyone's radar, so the necessary research can be done to find a cure. It must be horrible. I have a friend who suffers from it, so I am signing this to support her.
B
Belinda McNulty
12 years ago
I am one of the many people who suffer from this very painful condition and would much like to find a perminate cure for it.
We need this done asap
TN SUFFERER , we need a CURE
For Wendy...
Ladies and Gentlemen of WHO, Recognition and faster remedy for TN sufferers is PARAMOUNT. Not helping is equal to condemning these patients to life in a torture chamber....which is a Primal Fear of everyone on Earth. Please add Trigeminal Neuralgia to the Health Topics list. It is about being humane and civilized. Respectfully, Naomi di Gavriel Gertner
Supporting the ones I love
I am supporting LeeLeeBot who suffers from this terrible condition.
This disease is slowly, but surely, taking whatever quality of life I had away. Praying for relief.
Please find cause and cure.
I have a colleague who is suffering from this condition. Please find a way for TN to be cured.
Unbelievable that something like this can exist. Horrible. Hope they find a cure!!!!!
Please help stop the pain.
Please help raise awareness, help with research funding, help us get our lives back.
7 yrs now and 2 surgeries later. Still on Meds and told there isn't really anything they can do at this point because there just isn't alot of research out there to know how to fix it.
This is for you JEN!
I have bilateral TN1 &TN2
For TN sufferers the process of referral to treatment takes longer than it should... from onset to treatment is not much better either!! This is accross all nations, we wait longer, in agony, which results in suicide. There is no let up either we are in pain or feel like zombies. We take antiepilespy medication, the best bet there is, but still we get pain as we have no specific medication for our condition Please help us!!
hope is our only hope
HELP US FIND A CURE!!! I have TN on the right side of my face and it affects all branches.
Let's get this on everyone's radar, so the necessary research can be done to find a cure. It must be horrible. I have a friend who suffers from it, so I am signing this to support her.
I am one of the many people who suffer from this very painful condition and would much like to find a perminate cure for it.