Sitting Craniocervical MRI results

[Jules]

You might find this article interesting:

Red Lawhern, PhD's Advocacy Editorial

This was posted on the main moderator site, and I would like to share it with you. Red joined Ben's Friends to support his wife who suffers from TN (Trigeminal Neuralgia) he has become a moderator for that site, and an advocate for his wife and others who suffer this disease, he also often forwards new research info to our group on FMS, and hopes to expand his research into many other of our rare diseases! Thank you Red, and Thanks to Scott for posting it! http://www.mayoclinic.com/health/…

And these discussions might be helpful:

My Eagle Journey and Surgery

As reading other people’s stories has been so helpful to me, I thought I should share my story as well. In the spring of 2008, I had dental x-rays taken at my 6-month cleaning. The dentist noticed a long stick-like shadow on each side of my neck. As this perplexed him, he wanted a second opinion, so he sent me to another dentist for a Panoramic x-ray. Both of the long, stick-like shadows were even more visible and essentially identical. After much discussion, they concluded the structures i…

Long road, referred back to ENT for eagles

It seems you have run into the most deaf group of butchers who happen to have the MD after their name. who are these people?-even in AA if you take meds as prescribed its fine. Pain management is a whole profession un to itself and I was in it for 12 years and didn't ever have anybody question taking what was prescribed to me by one doctor. there is no need to judge you for taking meds as instructed. My pain management doctor finally agreed with me and told the medical board that it wasn't go…

There are a lot about TN, not necessarily just the maxillary branch. You can have a search of more if you need more info using the magnifying glass icon…I get the aching, constant pain, but in all 3 branches. It’s improved a lot since surgery, but not gone completely. Also Ben’s Friends have Chiari & Facial Pain groups if you want specific info on those, here’s the links if you’ve not seen these groups:
https://www.livingwithfacialpain.org/
https://www.bing.com/videos/search?q=bens+friends+chiari+malformation+group&docid=608048265157806659&mid=5D0C85A7D826322B00A95D0C85A7D826322B00A9&view=detail&FORM=VIRE
Hope this helps!