International Trigeminal Neuralgia Awareness Day October 7th!
5,071 Comments
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Susan Wiffill
9 years ago
Please accept that trigeminal neuralgia is a very real painful condition.even children an some animals can develop it.all we ask is for this horrendous pain is recognised by the world health organisation.please help us who suffer with this.if it is recognised by you,more research can be done,and hopefully there will be less suffering for all people and children .thank you
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Laura K Cunningham
9 years ago
This disease needs more attention. Please pay attention to this petition.
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Bonnie Swart
9 years ago
Disabled by TN for 15+ years.
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Anonymous
9 years ago
I'm TN patient. Medicine was helping for last 3 years. Pain comes back. Balloon compression is recommended. I'm open for other options.
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Cody Hubbard
9 years ago
My wife has TN, and she is an amazing Mother of 3 young boys who doesn't complain , but I know she is in extreme pain. Remember, God is good in the good times and bad.
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Michelle Celiz
9 years ago
I hate living like this.
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Marija Sijan
9 years ago
Research 4 a CURE
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Laylee Downing
9 years ago
Until this affected my immediate family, I had no idea it was so prevalent.
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Kay Laroche
9 years ago
Lost hope, seven years and counting......:(
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Lawrencia Hicks Forbes
9 years ago
I have Trigeminal Neuralgia.
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Yvonne Charles
9 years ago
I suffer with this disease every day. I'm tired of being in pain & being told that they are not sure what to do. We need a cute!
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Stacie L McConnell
9 years ago
Help us find relief
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NIPA DEY
9 years ago
Please try to find a cure
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Matt Stanford
9 years ago
Suffered for 15 years, it doesn't get easier, all my defenses are worn out. please help
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Edna Tutton
9 years ago
Let's get more research!!!
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Debra Ford
9 years ago
Please add this to your list of topics, this sounds too horrific to not do this!!
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Kim svoboda
9 years ago
I have suffered with TN and AD for 14 years. Please give us the research and time that this horrible disease deserves. Our lives are being taken away. I have to make decisions every day about what will give me quality of life and what will not. Everything is important so these decisions are never easy..
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Susan Wiffill
9 years ago
Please accept that this condition exists, WHO,So many people live their lives ruled by this pain. Medical workers know it exists,and if this is recognised by the WHO ,it will be so much more worthwhile. And those who suffer horrendous pain,will not just be dismissed so easily, when they are begging for help to stop the endless pain.it is not called the suicide disease for no reason. Seems more people find this pain unbearable to live with. Please help. Thankyou.
K
Kat
9 years ago
I have had TN since my 20's, it should be on the list.
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Rafael Marrero
9 years ago
MY WIFE HAS TN AND IVE NEVER SEEN SOMEONE IN SO MUCH PAIN
Please accept that trigeminal neuralgia is a very real painful condition.even children an some animals can develop it.all we ask is for this horrendous pain is recognised by the world health organisation.please help us who suffer with this.if it is recognised by you,more research can be done,and hopefully there will be less suffering for all people and children .thank you
This disease needs more attention. Please pay attention to this petition.
Disabled by TN for 15+ years.
I'm TN patient. Medicine was helping for last 3 years. Pain comes back. Balloon compression is recommended. I'm open for other options.
My wife has TN, and she is an amazing Mother of 3 young boys who doesn't complain , but I know she is in extreme pain. Remember, God is good in the good times and bad.
I hate living like this.
Research 4 a CURE
Until this affected my immediate family, I had no idea it was so prevalent.
Lost hope, seven years and counting......:(
I have Trigeminal Neuralgia.
I suffer with this disease every day. I'm tired of being in pain & being told that they are not sure what to do. We need a cute!
Help us find relief
Please try to find a cure
Suffered for 15 years, it doesn't get easier, all my defenses are worn out. please help
Let's get more research!!!
Please add this to your list of topics, this sounds too horrific to not do this!!
I have suffered with TN and AD for 14 years. Please give us the research and time that this horrible disease deserves. Our lives are being taken away. I have to make decisions every day about what will give me quality of life and what will not. Everything is important so these decisions are never easy..
Please accept that this condition exists, WHO,So many people live their lives ruled by this pain. Medical workers know it exists,and if this is recognised by the WHO ,it will be so much more worthwhile. And those who suffer horrendous pain,will not just be dismissed so easily, when they are begging for help to stop the endless pain.it is not called the suicide disease for no reason. Seems more people find this pain unbearable to live with. Please help. Thankyou.
I have had TN since my 20's, it should be on the list.
MY WIFE HAS TN AND IVE NEVER SEEN SOMEONE IN SO MUCH PAIN