International Trigeminal Neuralgia Awareness Day October 7th!

for Olivia

FIND A CURE

Find a way to cure their pain.

Please put this disease as high priority, as it is known as the suicide disease, and my sister in law died this past Aug with it. I saw first hand what this does to a person, as I cared for her until she died.

I have TN and it is a terrible thing. I am trusting to have surgery soon I will help as much as I can

There needs to be a cure an patients need to easily get access to Drs and treatments

We need the cure

I am 30 years old and I have suffered from trigeminal neuralgia for 9 years now. It is destroying my life. Each day is a battle.

My name is Adriean and I suffer from Trigeminal Neuralgia. I am signing this petition because, as anyone with an invisible illness will tell you, global awareness and knowledge of the illness can make all the difference in the world. It can open up the opportunity for scientific studies, medical trials, and the development of new medications to help calm the effects of attacks. Please add TN to your topics list, we need help!

Additional research would be great help.

People need to be aware & educated of this awful illness.

Doing this for my beautiful cousin who has been so strong throughout dealing with trigeminal neuralgia

I have this disease and it is horrible! I don't understand how people with social anxiety get recognized but not Trigeminal Neuralgia.

I was diagnosed with TN a month ago after a dental injection in Jan 2017.

Thank you to the WHO for your help and support for those of us who suffer!

Trigeminal Neuralgia is a living hell!

My boss has this and I never realized how bad the pain is. What a brave and strong lady!

Awareness is key to treatment or even cure

Please help all of us who are suffering... please this just as important as any other disease out there except this one we have no cure or too much help with it. Please we beg you as a suffer myself. Christina Bell

I have Trigeminal Neuralgia and have a rare bilateral form of it. I have found that after 11 neurologist I have only been able to find one that has even seen a patient like me. And 9 of the 11 knew less about the disease then myself. We need more awareness, information, and education out there not only for support but for the medical community as well. One admitted they were only taught about bilateral patients in 2 paragraphs during their schooling. That is no where near enough concidering the neurologist is our primary care provider for this disease. Adding TN to your list will open more doors all the way around.