Hi all, I believe there is a reason for everything and with that I think my purpose is to get the word out about Trigemjnal Neuralgia! I want everyone to know that it's real and folk suffer with it everyday! I would like to start a support group because when you're able to talk you want people to help you and not pity you. Are there any procedures that i need to follow in order to start a group for people living in the Memphis and surrounding areas? People need to know about this disease and what folk diagnosed with it live with each day....any help would be greatly appreciated!
I live in the Memphis area. Please keep me updated.
Michelle…thank you will do! I’m scheduled for hopefully my first and only MVD surgery on December 17th in Nashville so my plan is to get the plan together while recuperating!