International Trigeminal Neuralgia Awareness Day October 7th!
5,071 Comments
S
Sharon Goins
11 years ago
This is devastating disease..I've lost years of my life, in doctor's office's...It's real, it hurts, and it debilitating ...TN is for real!!!!!!
J
jennifer citak
11 years ago
because no one should go through this horrific condition alone- we all need one another and all possible help,information and support available ...
S
sandra frechette
11 years ago
Because every disease is worth finding a cure !
M
michael keehan
11 years ago
for maddy..
M
Melanie DeDecker Johnson
11 years ago
I support TN sufferers and push for WHO to add TN to lists of diseases for study.
R
Ruth Ann Hennick
11 years ago
Iam have TN since feb 2, 2014 it hit on my 54 birthday what birthday gift. y pain is in my lower jaw on both sides. cold & breezes hurts my jaw. m i take Gabapentin 300 mg 3 x a day /. the pain makes me cry alot.Ruth Ann ps i want blue ribbion. send to me 532cdaisy drive taneytown, maryland, 22787
A
amy thiboutot
11 years ago
Good luck!!!!!!!
C
Cheryl Nielsen
11 years ago
I am currently a victim of this illness. We need a cure!!!
Y
yakub Karim
11 years ago
This disease should be classified as a Disability.
Y
yakub Karim
11 years ago
This disease should be classified as a Disability.
L
Lawrence Cuttler
11 years ago
I suffer from TN. It returned after 20 years. Cannot take Medications that have terrible side effects.
E
Elvira Buck
11 years ago
I have suffered from this terrible disease for 4 yrs. I had surgery 2 yrs ago with no results.
Thanks
L
Louise Ferrazzano
11 years ago
Please help those who also have TN type 2. We have been classified as atypical because our symptoms are unusual .We need more awareness on this "atypical" type.
R
Ronald Streich
11 years ago
It took years of doctor exams to receive my diagnosis of Type 2 TN. Reporting on TN therapies including pharmacological and neurosurgery has been abysmal and the internet reporting by patients is only beginning to show the large affected population numbers. EEG diagnosis has been the only consistent diagnostic tool but it is seldom done because it takes more than 15 minutes and is not highly profitable.
C
Connie Needler
11 years ago
I suffer from this daily.
R
Rose Arnerich
11 years ago
please help us to cure this terrible disease.
A
Amy
11 years ago
Please help us spread awareness and find a much needed cure for Trigeminal Neuralgia.
Thank you,
Amy
J
Jane Whittaker
11 years ago
please help, people are struggling all over the world with this horrible disorder
J
jeritta lawrence
11 years ago
we really need help to get this petition pushed through. This disease has definitely earned its nickname of "the suicide disease" I know from my experience I have thought of it when the pain has been at its worst. W
Please let's get more awareness and help.
G
Gail Norris
11 years ago
I suffer from TN and urge you to take action on this disease.
This is devastating disease..I've lost years of my life, in doctor's office's...It's real, it hurts, and it debilitating ...TN is for real!!!!!!
because no one should go through this horrific condition alone- we all need one another and all possible help,information and support available ...
Because every disease is worth finding a cure !
for maddy..
I support TN sufferers and push for WHO to add TN to lists of diseases for study.
Iam have TN since feb 2, 2014 it hit on my 54 birthday what birthday gift. y pain is in my lower jaw on both sides. cold & breezes hurts my jaw. m i take Gabapentin 300 mg 3 x a day /. the pain makes me cry alot.Ruth Ann ps i want blue ribbion. send to me 532cdaisy drive taneytown, maryland, 22787
Good luck!!!!!!!
I am currently a victim of this illness. We need a cure!!!
This disease should be classified as a Disability.
This disease should be classified as a Disability.
I suffer from TN. It returned after 20 years. Cannot take Medications that have terrible side effects.
I have suffered from this terrible disease for 4 yrs. I had surgery 2 yrs ago with no results. Thanks
Please help those who also have TN type 2. We have been classified as atypical because our symptoms are unusual .We need more awareness on this "atypical" type.
It took years of doctor exams to receive my diagnosis of Type 2 TN. Reporting on TN therapies including pharmacological and neurosurgery has been abysmal and the internet reporting by patients is only beginning to show the large affected population numbers. EEG diagnosis has been the only consistent diagnostic tool but it is seldom done because it takes more than 15 minutes and is not highly profitable.
I suffer from this daily.
please help us to cure this terrible disease.
Please help us spread awareness and find a much needed cure for Trigeminal Neuralgia. Thank you, Amy
please help, people are struggling all over the world with this horrible disorder
we really need help to get this petition pushed through. This disease has definitely earned its nickname of "the suicide disease" I know from my experience I have thought of it when the pain has been at its worst. W Please let's get more awareness and help.
I suffer from TN and urge you to take action on this disease.