International Trigeminal Neuralgia Awareness Day October 7th!
5,071 Comments
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Nancy Bayer
11 years ago
This disease has ruined my life in every aspect. I have no ability to work, no resources for help, and have such intense symtoms even TN suffered cannot understand. Experimental procedures are getting a 1 inch hole drilled in our head and having someone play with our brain stem with very little chance at a cure but yes I signed up for that only to wait another year in constant pain in addition to the las 7 months.
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Nancy Bayer
11 years ago
This disease has ruined my life in every aspect. I have no ability to work, no resources for help, and have such intense symtoms even TN suffered cannot understand. Experimental procedures are getting a 1 inch hole drilled in our head and having someone play with our brain stem with very little chance at a cure but yes I signed up for that only to wait another year in constant pain in addition to the las 7 months.
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Marie bradshaw
11 years ago
I have TN and it affects not only myself but my children are now my carers. . We need help ..
M
Marie bradshaw
11 years ago
I have TN and it affects not only myself but my children are now my carers. . We need help ..
L
Linéa Marketos
11 years ago
Although relatively small in number, TN sufferers are near the top of the painful condition list. No one should have to suffer so, especially with a condition that isn't even on WHO's Health Topics List
L
Linéa Marketos
11 years ago
Although relatively small in number, TN sufferers are near the top of the painful condition list. No one should have to suffer so, especially with a condition that isn't even on WHO's Health Topics List
M
mario acevedo
11 years ago
I am a father of a lovely young daughter
That fight evry day with the trigeminal neuralgia and still fighting for 11 years.my support and solidarity with all parents and all patients that suffer , blessings for all....
M
mario acevedo
11 years ago
I am a father of a lovely young daughter
That fight evry day with the trigeminal neuralgia and still fighting for 11 years.my support and solidarity with all parents and all patients that suffer , blessings for all....
J
Jennifer Chambers
11 years ago
Hoping for the possibility of more awareness which can hopefully lead to research towards a cure.
J
Jennifer Chambers
11 years ago
Hoping for the possibility of more awareness which can hopefully lead to research towards a cure.
S
Shelly Stroud
11 years ago
Team Cheryl
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Shelly Stroud
11 years ago
Team Cheryl
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Carrie Maynard
11 years ago
In support of my friend Cheryl Orlet.
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Carrie Maynard
11 years ago
In support of my friend Cheryl Orlet.
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Robyn
11 years ago
Someone I hold dearly to my heart suffers from trigeminal neuralgia, and it's heartbreaking to watch her suffer. although she is strong and holds her head up she has 3 kids she tries to be strong for and this disease sometimes keeps her from playing and interacting with them. It keeps her up at night and she has gone through surgery, multiple shots, and medications to try to help the pain and nothing has helped.
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Robyn
11 years ago
Someone I hold dearly to my heart suffers from trigeminal neuralgia, and it's heartbreaking to watch her suffer. although she is strong and holds her head up she has 3 kids she tries to be strong for and this disease sometimes keeps her from playing and interacting with them. It keeps her up at night and she has gone through surgery, multiple shots, and medications to try to help the pain and nothing has helped.
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Chasidy Smith
11 years ago
I had never heard of this horrible disease before my sister was diagnosed. More research needs to be done and people need to be aware of this.
C
Chasidy Smith
11 years ago
I had never heard of this horrible disease before my sister was diagnosed. More research needs to be done and people need to be aware of this.
This disease has ruined my life in every aspect. I have no ability to work, no resources for help, and have such intense symtoms even TN suffered cannot understand. Experimental procedures are getting a 1 inch hole drilled in our head and having someone play with our brain stem with very little chance at a cure but yes I signed up for that only to wait another year in constant pain in addition to the las 7 months.
This disease has ruined my life in every aspect. I have no ability to work, no resources for help, and have such intense symtoms even TN suffered cannot understand. Experimental procedures are getting a 1 inch hole drilled in our head and having someone play with our brain stem with very little chance at a cure but yes I signed up for that only to wait another year in constant pain in addition to the las 7 months.
I have TN and it affects not only myself but my children are now my carers. . We need help ..
I have TN and it affects not only myself but my children are now my carers. . We need help ..
Although relatively small in number, TN sufferers are near the top of the painful condition list. No one should have to suffer so, especially with a condition that isn't even on WHO's Health Topics List
Although relatively small in number, TN sufferers are near the top of the painful condition list. No one should have to suffer so, especially with a condition that isn't even on WHO's Health Topics List
I am a father of a lovely young daughter That fight evry day with the trigeminal neuralgia and still fighting for 11 years.my support and solidarity with all parents and all patients that suffer , blessings for all....
I am a father of a lovely young daughter That fight evry day with the trigeminal neuralgia and still fighting for 11 years.my support and solidarity with all parents and all patients that suffer , blessings for all....
Hoping for the possibility of more awareness which can hopefully lead to research towards a cure.
Hoping for the possibility of more awareness which can hopefully lead to research towards a cure.
Team Cheryl
Team Cheryl
In support of my friend Cheryl Orlet.
In support of my friend Cheryl Orlet.
Someone I hold dearly to my heart suffers from trigeminal neuralgia, and it's heartbreaking to watch her suffer. although she is strong and holds her head up she has 3 kids she tries to be strong for and this disease sometimes keeps her from playing and interacting with them. It keeps her up at night and she has gone through surgery, multiple shots, and medications to try to help the pain and nothing has helped.
Someone I hold dearly to my heart suffers from trigeminal neuralgia, and it's heartbreaking to watch her suffer. although she is strong and holds her head up she has 3 kids she tries to be strong for and this disease sometimes keeps her from playing and interacting with them. It keeps her up at night and she has gone through surgery, multiple shots, and medications to try to help the pain and nothing has helped.
I had never heard of this horrible disease before my sister was diagnosed. More research needs to be done and people need to be aware of this.
I had never heard of this horrible disease before my sister was diagnosed. More research needs to be done and people need to be aware of this.
For Cheryl Orlet and Debbie Murphy
For Cheryl Orlet and Debbie Murphy