International Trigeminal Neuralgia Awareness Ribbon
We share the color teal with awareness for Ovarian Cancer.
October 7th, is the International Awareness Day for Trigeminal Neuralgia and Facial Pain Disorders
Facial Pain Advocacy Alliance Donations from the purchase of the International TN Awareness Ribbon will help us raise funds for research to find a cure for Trigeminal Neuralgia and Facial Pain Disorders at the Facing Facial Pain Research Foundation and at the Facial Pain Association.
To purchase our Intl TN Awareness Ribbon > BUY NOW
We're asking the World Health Organization (WHO) to take action on Trigeminal Neuralgia & Facial Pain Disorders!
WHO, Please add Trigeminal Neuralgia to the "Health Topics" list!
By WHO including TN on their listing of health issues which could broaden awareness, having access to resources and create opportunities with regards to financing as well as researching.
We need to educate individuals associated with trigeminal neuralgia and it's characteristic, signs and symptoms as well as treatment options. Joining each of our voices collectively, we are able to be heard all over the world!
The Facial Pain Association is a 501 (c)(3) non-profit, voluntary health organization, serving patients world-wide who suffer from neuropathic face pain, including trigeminal neuralgia (TN), their families and the physicians, dentists and healthcare providers who treat them. TNA provides one-on-one patient support through it's toll-free telephone lines and its website and helps maintain over 50 local support groups throughout the USA, Canada, Europe and Australia.
Facial Pain Research Foundation aims to turn a page in history by finding a cure for the world's most excruciating pain.
Finding a cure for trigeminal neuralgia, the most painful disorder known to humans, is the mission of The Facial Pain Research Foundation. The Foundation is the brainchild of seven professionals across the United States, who are creating the first international force of scientists to work together to cure an ancient, but poorly understood diseases. Finding a cure will restore pain-free life to millions of men, women and children around the world, who are stricken by repeated lightning-like shocks of facial pain, the hallmark of trigeminal neuralgia.
Trigeminal neuralgia was first identified in the 11th century, yet it remains frequently misdiagnosed and inappropriately treated, in many cases resistant to the best available therapies, and tragically linked to depression, fear, fatigue, and suicide. The pain has a bizarre “hit and run” behavior; it strikes near the eyes, nose, lips, ears or teeth, sometimes disappears for days, months or longer, then returns. The pain seems to come out of nowhere with a stabbing intensity that stops life in its tracks and draws full attention to the need to find relief.
More info on: What is Trigeminal Neuralgia and Facial Pain Disorders
Web-sites and public support pages to educate, raise awareness and share the latest information about TN, information to help you cope with the pain, etc. This information is provided for all to share.
Here are a few links:
EndTN
Facial Pain Advocacy Alliance
Facial Pain Research Foundation FB page
Facial Pain Association FB Page
LivingwithFacialPain Web-site
TNAC Trigeminal Neuralgia Association of Canada
Trigeminal Neuralgia Association UK Facing Pain Together
Trigeminal Neuralgia Association Australia
Trigeminal Neuralgia Support New Zealand
CaTNA Canadian Trigeminal Neuralgia Association
Association Quebecois De La Douleur Chronigue
AFAT (Association Francaise Algies Trigeminal)
Ireland Support Group
Teens with Trigeminal Neuralgia
Alaska Trigeminal Neuralgia
To purchase our Intl TN Awareness Ribbon > BUY NOW
We're asking the World Health Organization (WHO) to take action on Trigeminal Neuralgia & Facial Pain Disorders!
WHO, Please add Trigeminal Neuralgia to the "Health Topics" list!
By WHO including TN on their listing of health issues which could broaden awareness, having access to resources and create opportunities with regards to financing as well as researching.
We need to educate individuals associated with trigeminal neuralgia and it's characteristic, signs and symptoms as well as treatment options. Joining each of our voices collectively, we are able to be heard all over the world!
The Facial Pain Association is a 501 (c)(3) non-profit, voluntary health organization, serving patients world-wide who suffer from neuropathic face pain, including trigeminal neuralgia (TN), their families and the physicians, dentists and healthcare providers who treat them. TNA provides one-on-one patient support through it's toll-free telephone lines and its website and helps maintain over 50 local support groups throughout the USA, Canada, Europe and Australia.
Facial Pain Research Foundation aims to turn a page in history by finding a cure for the world's most excruciating pain.
Finding a cure for trigeminal neuralgia, the most painful disorder known to humans, is the mission of The Facial Pain Research Foundation. The Foundation is the brainchild of seven professionals across the United States, who are creating the first international force of scientists to work together to cure an ancient, but poorly understood diseases. Finding a cure will restore pain-free life to millions of men, women and children around the world, who are stricken by repeated lightning-like shocks of facial pain, the hallmark of trigeminal neuralgia.
Trigeminal neuralgia was first identified in the 11th century, yet it remains frequently misdiagnosed and inappropriately treated, in many cases resistant to the best available therapies, and tragically linked to depression, fear, fatigue, and suicide. The pain has a bizarre “hit and run” behavior; it strikes near the eyes, nose, lips, ears or teeth, sometimes disappears for days, months or longer, then returns. The pain seems to come out of nowhere with a stabbing intensity that stops life in its tracks and draws full attention to the need to find relief.
More info on: What is Trigeminal Neuralgia and Facial Pain Disorders
Web-sites and public support pages to educate, raise awareness and share the latest information about TN, information to help you cope with the pain, etc. This information is provided for all to share.
Here are a few links:
EndTN
Facial Pain Advocacy Alliance
Facial Pain Research Foundation FB page
Facial Pain Association FB Page
LivingwithFacialPain Web-site
TNAC Trigeminal Neuralgia Association of Canada
Trigeminal Neuralgia Association UK Facing Pain Together
Trigeminal Neuralgia Association Australia
Trigeminal Neuralgia Support New Zealand
CaTNA Canadian Trigeminal Neuralgia Association
Association Quebecois De La Douleur Chronigue
AFAT (Association Francaise Algies Trigeminal)
Ireland Support Group
Teens with Trigeminal Neuralgia
Alaska Trigeminal Neuralgia
You can make a tax Deductible Donation right now.
CLICK THE DONATE BUTTON...or
Send Check To:
The Facial Pain Research Foundation
2653 SW 87th Drive, Suite A
Gainesville FL 32608-9313
CLICK THE DONATE BUTTON...or
Send Check To:
The Facial Pain Research Foundation
2653 SW 87th Drive, Suite A
Gainesville FL 32608-9313
Below Links on how YOU can spread awareness for Trigeminal Neuralgia and Facial Pain Disorders
Intl TN Awareness Petition
TN/FP Resource
Intl TN Awareness Ribbon
TN Awareness Products
TN Awareness To Do List
TN/FP Awareness Videos
TN Short Stories by Brian Whitaker
What is Trigeminal Neuralgia?
What is Facial Pain Disorders?
What is the Battle Scars of TN/FP?
How to Donate to the Facial Pain Research Foundation?
Why is Trigeminal Neuralgia classified at G50?
Letter to the World Health Organization
Open Letter to Dentist and Oral Surgeons
Open Letter to Doctors
Open Letter to Emergency Room Doctors
2018 Light Up Teal Locations
How to request “Light Up Teal” for 2018?
Help support Trigeminal Neuralgia and Facial Pain Disorders simply by spreading Awareness!
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