Trigeminal Neuralgia and Facial Pain Disorders Support
Resources for support and information below
A Big Thank You and Blessing to the Author of this page Lorraine Burgess [Trigeminal Neuralgia NL]
Trigeminal Neuralgia Support Newfoundland & Labrador
Trigeminal Neuralgia Support Newfoundland & Labrador
Every day I see new people joining support groups and coming to support and information pages.
Many of you tell us how happy you are to find someone who understands what you are going through and that you are no longer alone.
I also see posts asking about how to raise awareness for trigeminal neuralgia and facial pain.
Some of you don't know yet about all the dedicated people around the world who are working hard to make sure that fellow TNers, the newly diagnosed, and everyone who suffers from facial pain are not alone in their struggle.
There are some very dedicated and hard working groups and individuals who are working to let the world know about this disease Trigeminal Neuralgia and other facial pains.
There are people who create private support groups so you can have a safe and private place to share your stories and learn from each other. There are too many to list here, but you will find a list of international support sites on our support page.
Support Links:
Kentucky Trigeminal Neuralgia Support Group Facebook
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
Ireland Support Group
Teens with Trigeminal Neuralgia
Alaska Trigeminal Neuralgia
Many of you tell us how happy you are to find someone who understands what you are going through and that you are no longer alone.
I also see posts asking about how to raise awareness for trigeminal neuralgia and facial pain.
Some of you don't know yet about all the dedicated people around the world who are working hard to make sure that fellow TNers, the newly diagnosed, and everyone who suffers from facial pain are not alone in their struggle.
There are some very dedicated and hard working groups and individuals who are working to let the world know about this disease Trigeminal Neuralgia and other facial pains.
There are people who create private support groups so you can have a safe and private place to share your stories and learn from each other. There are too many to list here, but you will find a list of international support sites on our support page.
Support Links:
Kentucky Trigeminal Neuralgia Support Group Facebook
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
Ireland Support Group
Teens with Trigeminal Neuralgia
Alaska Trigeminal Neuralgia
They post to Newspapers, TV programs, send emails to Governments, Health Professionals, and anyone or anywhere else they can, to raise awareness with the public about TN and Facial pain. See Our TN Stories
There is an official TN awareness ribbon that brings awareness and donations to the Facial Pain Research Foundations.
On October 7th our International Trigeminal Neuralgia Awareness Day, there will be bridges, monuments and buildings around the world lighting up Teal.
Fellow TNers who write blogs, do interviews with newspapers, television programs, on YouTube and other social media. By telling their personal stories, these courageous, but normally very private people, have shown the world what it is like to live with this horrific, painful, debilitating disease.
You are no longer alone.
Many of these people are like yourselves, living with the pain every day or watching their loved ones suffer from the pain.
Even If they are pain-free now, they still share the same fear that the pain will return.
They all work hard to do this, but they cannot do it alone.
They need each and every one of you to do whatever you can to raise awareness of trigeminal neuralgia and facial pain.
Write letters to your local newspapers, TV stations, radio stations, politician and share everything you can about TN on your Facebook pages to educate your family and friends about this horrific disease.
Every time you tell your story about living with TN, write a letter, send an email, share a post, brings us one step closer to raising awareness of trigeminal neuralgia / facial pain and ending the pain.
What everyone wants and needs is a cure. The truth is that even with all this hard work, educating the public and each other, it will not happen unless this can translate into funding for research. There are clinical trials for new and better drugs, research into new ways to see inside the brain and new surgery's. All this is good, but it is not research to find a cure.
The only organization, that we know about, who is doing research to find a cure is the Facial Pain Research Foundation. Finding a cure for trigeminal neuralgia, the most painful disorder known to humans, is the mission of The Facial Pain Research Foundation. Its founders aim to reach the goal within the decade of 2011-2020 while also developing therapies to permanently stop other nerve-generated facial pains and diseases. They need our help to raise the money to fund this research.
I realize that money is very limited for most TN sufferers because of the health cost and loss of income for many people but every little bit helps. We are encouraged to see posts where TN sufferers are telling their friends and family that instead of giving gifts for birthdays, weddings, Christmas, etc., they are asking for donations to be made to the foundation to help find a cure. This is where my donations go, not only for my family but for everyone who suffers from TN and Facial Pain. Finding a cure will restore pain-free life not just for this generation but for future generations, to millions of men, women and children around the world. I don't expect everyone to do this, but I would like you to consider donating a small portion of your gift-giving budgets in your family's name or make it a gift to yourself. What better gift can you give yourself, or others, than the gift of hope for a cure
If you decide to donate this is the link to the donation page. This website will also tell you where and how your money is used to fund research for a cure. http://www.facingfacialpain.org/
Thank you
Lorraine Burgess [Trigeminal Neuralgia NL]
Trigeminal Neuralgia Support Newfoundland & LabradorContact Info:
I can't thank Lorraine enough for all the work and time she has put into words to make sure everyone knows we're working together to raise awareness for Trigeminal Neuralgia and Facial Pain Disorders! Toni Saunders...aka..TNnME
Bring awareness to our TNA/FPA Associations and Support Groups.
The Facial Pain Association
The Facial Pain Research Foundation
Trigeminal Neuralgia Association of Canada TNAC
Trigeminal Neuralgia Association UK (TNA UK)
Canadian TN Association CaTNA
Trigeminal Neuralgia Association Australia
Ireland Support Group
Teens with Trigeminal Neuralgia_
Alaska Trigeminal Neuralgia Support Group Facebook Page
International Resources:
USA: Working Together
Brazil
Finland
United Kingdom
Netherlands
Canada
There is an official TN awareness ribbon that brings awareness and donations to the Facial Pain Research Foundations.
On October 7th our International Trigeminal Neuralgia Awareness Day, there will be bridges, monuments and buildings around the world lighting up Teal.
Fellow TNers who write blogs, do interviews with newspapers, television programs, on YouTube and other social media. By telling their personal stories, these courageous, but normally very private people, have shown the world what it is like to live with this horrific, painful, debilitating disease.
You are no longer alone.
Many of these people are like yourselves, living with the pain every day or watching their loved ones suffer from the pain.
Even If they are pain-free now, they still share the same fear that the pain will return.
They all work hard to do this, but they cannot do it alone.
They need each and every one of you to do whatever you can to raise awareness of trigeminal neuralgia and facial pain.
Write letters to your local newspapers, TV stations, radio stations, politician and share everything you can about TN on your Facebook pages to educate your family and friends about this horrific disease.
Every time you tell your story about living with TN, write a letter, send an email, share a post, brings us one step closer to raising awareness of trigeminal neuralgia / facial pain and ending the pain.
What everyone wants and needs is a cure. The truth is that even with all this hard work, educating the public and each other, it will not happen unless this can translate into funding for research. There are clinical trials for new and better drugs, research into new ways to see inside the brain and new surgery's. All this is good, but it is not research to find a cure.
The only organization, that we know about, who is doing research to find a cure is the Facial Pain Research Foundation. Finding a cure for trigeminal neuralgia, the most painful disorder known to humans, is the mission of The Facial Pain Research Foundation. Its founders aim to reach the goal within the decade of 2011-2020 while also developing therapies to permanently stop other nerve-generated facial pains and diseases. They need our help to raise the money to fund this research.
I realize that money is very limited for most TN sufferers because of the health cost and loss of income for many people but every little bit helps. We are encouraged to see posts where TN sufferers are telling their friends and family that instead of giving gifts for birthdays, weddings, Christmas, etc., they are asking for donations to be made to the foundation to help find a cure. This is where my donations go, not only for my family but for everyone who suffers from TN and Facial Pain. Finding a cure will restore pain-free life not just for this generation but for future generations, to millions of men, women and children around the world. I don't expect everyone to do this, but I would like you to consider donating a small portion of your gift-giving budgets in your family's name or make it a gift to yourself. What better gift can you give yourself, or others, than the gift of hope for a cure
If you decide to donate this is the link to the donation page. This website will also tell you where and how your money is used to fund research for a cure. http://www.facingfacialpain.org/
Thank you
Lorraine Burgess [Trigeminal Neuralgia NL]
Trigeminal Neuralgia Support Newfoundland & LabradorContact Info:
I can't thank Lorraine enough for all the work and time she has put into words to make sure everyone knows we're working together to raise awareness for Trigeminal Neuralgia and Facial Pain Disorders! Toni Saunders...aka..TNnME
Bring awareness to our TNA/FPA Associations and Support Groups.
The Facial Pain Association
The Facial Pain Research Foundation
Trigeminal Neuralgia Association of Canada TNAC
Trigeminal Neuralgia Association UK (TNA UK)
Canadian TN Association CaTNA
Trigeminal Neuralgia Association Australia
Ireland Support Group
Teens with Trigeminal Neuralgia_
Alaska Trigeminal Neuralgia Support Group Facebook Page
International Resources:
USA: Working Together
Brazil
Finland
United Kingdom
Netherlands
Canada
Disclaimer:
All information contained on TNnME web site is for informational purposes only and at no time should any content on TNNME be considered medical or legal advice or imply any action should be taken. It is in no way intended to be used as a replacement for professional medical treatment. TNnME makes no claims as to the scientific/clinical validity of the information on this site OR to that of the information linked to and from this site. All information taken from the internet should be discussed with a medical professional!
All information contained on TNnME web site is for informational purposes only and at no time should any content on TNNME be considered medical or legal advice or imply any action should be taken. It is in no way intended to be used as a replacement for professional medical treatment. TNnME makes no claims as to the scientific/clinical validity of the information on this site OR to that of the information linked to and from this site. All information taken from the internet should be discussed with a medical professional!
Photos used under Creative Commons from JoanDragonfly homegets.com
