Glossopharyngeal Neuralgia (GPN) - Online Support Group

We are patients living with glossopharyngeal neuralgia, here for your support.

About Us

What is LivingWithGPN.org?

LivingWithGPN.org is a dedicated patient-to-patient support community for families affected by Glossopharyngeal Neuralgia. LivingWithGPN.org is powered by BensFriends.org, patient support communities for rare diseases, and is run by volunteer moderators who have been affected with Glossopharyngeal Neuralgia.

 

Who can join LivingWithGPN.org?

 

If your family has been affected by Glossopharyngeal Neuralgia, consider LivingWithGPN.org your second home. LivingWithGPN.org, as well as the rest of BensFriends.org’s patient communities, is free for members to join.

 

What is Glossopharyngeal Neuralgia?

Glossopharyngeal Neuralgia is “chronic pain syndrome that causes intense, shooting pains in the back of the tongue and throat, tonsillar areas, and middle ear.”

 

You can learn more about Fibromyalgia at HealthLine.

 

What is BensFriends.org?

In 2007, Ben Muñoz suffered a rare form of stroke caused by an AVM. He was unable to find the support he needed during the most difficult time, so he created an online support community AVMSurvivors.org to connect with others like him. AVMSurvivors.org led to the founding of BensFriends.org, driven to provide patient-to-patient support communities for people living with rare diseases.

 

BensFriends.org is a network of patient communities for people living with rare diseases. Launched in November 2007, BensFriends.org provides valuable patient support by creating and running compassionate, responsive communities. BensFriends.org maintains dozens of patient communities and has changed thousands of lives.

 

You can learn more about BensFriends.org at http://www.bensfriends.org or watch one of our videos at http://www.youtube.com/BensFriendsVideos.

Please Like Us On Facebook and Follow Ben's Friends on Tumblr and Twitter

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Blog Posts

May 2012 LivingwithGPN Community Newsletter

Posted by Ben Munoz on May 26, 2012 at 6:42am 0 Comments

Dear Friends and Family of LivingWithGPN,

We are so excited we cannot wait to tell you about how our organization is growing, so we’ll go straight at it. We are please to tell you that collectively our patient communities…

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No Eagles Syndrome

Posted by Denise on May 23, 2012 at 11:05pm 0 Comments

My styloid process and tonsils have been removed and no relief from the pain.  It is actually worse. Unfortunately, it doesn't seem as though it was Eagles Syndrome.  Back to my GPN diagnosis.  UGH!  I am starting a stronger pain medicine this…

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