International Trigeminal Neuralgia Awareness Day October 7th!

TNnME Intl TN Awareness Fighters
TNnME Intl TN Awareness Fighters Worldwide 4321 Comments
26,127 Signatures Goal: 40,000

Created and Sponsor by TNnME (Trigeminal Neuralgia and Me) and the International TN Awareness Fighters from around the world.

We're asking the World Health Organization (WHO): To take action regards to Trigeminal Neuralgia, ALL Neuralgias, and Facial Pain Disorders by adding Trigeminal Neuralgia to their "Health Topics" list.

This year awareness campaign is dedicated to @WHO we are! @WHO I am and how @WHO (World Health Organization) can help withTrigeminal Neuralgia and Facial Pain Disorders. By adding Trigeminal Neuralgia to your health topic list, this will also open doors for all neuralgia and facial pain disorders! It will create awareness, access to resources and create opportunities for funding & research.

TN is...characterized by episodes of intense pain in the face originating from the Trigeminal Nerve. The pain felt is the most excruciating known to man. This condition is so rare that only 1 in 20,000 people have it as some might say, but that number could be higher due to misdiagnosis. Women are more likely than men to be affected. Usually those older than 50 are diagnosed, but you can have it as young as 3 yrs. old!

People signing this petition are supporting Oct. 7th as the official International Awareness Day for Trigeminal Neuralgia and Facial Pain Disorders and asking (WHO) to add Trigeminal Neuralgia to their “Health Topic List”

We must inform people of what Trigeminal Neuralgia is, it's characteristic, symptoms & treatments. Joining our voices together, we can be heard around the world!

NO $ needed for your signature on this petition just your name, email address, then hit the "Sign Now" button and close out. Support Trigeminal Neuralgia & Facial Disorders by spreading Awareness!

http://www.fpa-support.org/for online facial pain support

The International TN Awareness Ribbon is available for your purchase, with funds going to the above Facial Pain Association and the below Facing Facial Pain Research Foundation to do research for a CURE.

Sponsor

Tnnme.com and Trigeminal Neuralgia Awareness Fighters. contact: tnnme and the awareness fighters at: tnawareness@gmail.com

Links

  • Anonymous
    Anonymous
    Nov 20, 2017
    Nov 20, 2017
    Help us please!
  • Sharon Lidderdale
    Sharon Lidderdale United States, Northfield
    Nov 19, 2017
    Nov 19, 2017
    I have TN and currently get ssd
  • Anonymous
    Anonymous
    Nov 17, 2017
    Nov 17, 2017
    This disease is extremely painful and needs to be on the list.
  • Sandra Carino
    Sandra Carino United States, Port Orchard
    Nov 17, 2017
    Nov 17, 2017
    We are not as RARE as the medical field think. More dollars are need to do my research for a CURE. Thanks
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Signatures

  • 5 days ago
    Mina Tovar United States
    5 days ago
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    Barbara Muldowney United States
    5 days ago
  • 6 days ago
    Sharon Lidderdale United States
    6 days ago
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    Anna Maria cesqui Italy
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    Sandra Carino United States
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    Steve Barnes United States
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    Linda Somma United States
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    Erin M McNeil United States
    2 weeks ago
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    Natalie dePena United States
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    Erin Schulten United States
    3 weeks ago
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    Darren Glase Australia
    3 weeks ago
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    Jenn W United States
    3 weeks ago
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    Lissette Wesby United States
    3 weeks ago
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    Joy Magill United States
    3 weeks ago
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    Catherine Colon United States
    3 weeks ago
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