International Trigeminal Neuralgia Awareness Day October 7th!

Please help all of us

Have a very good friend who is blighted by this dreadful disorder.

Diagnosed in 2012. Please find a cure!

More research for better diagnoses and a cure are needed.

There needs to be more funding to find a cure or better treatments. This disease is poorly treated in ERs and i have watched my love one for 16 yrs in agony debilitated and cannot even get disability. Its devastating and absolutely horrible to watch and cant imagine being the one having to endure the pain. Raise awareness. We need a cure for this horrid disease!!

Please be an advocate for all of us TN sufferers. Thank you!

I have TN and the impact it has had on my quality of life and ability to work is unbelievable. There is no support or help available from centrelink or Dhs, there is no cure and it can take years to find the right treatment mix to be able to cope with daily challenges. Please sign this petition to have TN recognised

Cure is badly needed.

I've been in extreme pain since 2003 as a result of a mva. Brachial plexus nerve avulsion and spinal cord injury is the root of my pain and if TN is cosidered worst pain known to man WHO must have no option but to put TN on their Health Topics list.

It is high time TN cure research was properly funded - too many people are suffering. TN is affecting many young people despite all the available guidance saying it is mostly common in over 50s. There are more cases of bilateral TN despite current information stating TN is rarely bilateral. Basically, the available information is outdated. There has to be more that can be done in this day and age! Our pets would not be allowed/expected to live with that level of pain. We simply can no longer accept status quo!

Please!

We need your help. Urgently. Thanks

Please help find a cure for this severely painful and frightening difficult condition. Thank you.

We need your help, please.

Please add to list

I have Trigeminal Neualgia for the past 10 years.

Please help!

My mom has TN. We are from South Africa...and the treatment here fot TN is even less then the rest of the world. My mom realy has a very difficult time with this desease. But she is the breavest person i know. More awerness for TN is needed word wide!!!!

Please add this painful condition. We need to find solutions to cure this. It should not be dependent on the number of people who suffer but the degree to which we suffer. We need help

I have it on both sides with no support. Please make this a national health awareness.