This is a place to share our stories, our hopes, our questions, our triumphs, and our frustrations about meningioma brain tumors. Isolation can be as hard to deal with as the tumor itself. This site is here to help ease the effects of isolation, and to help people get on with their life after diagnosis. Please let us hear from you. You will need to join the group to post a message. Any message you post will be sent to all the members who have elected to receive them. A copy of each message is available here at the web site. If you prefer a bulletin board format for a discussion, visit "Meningioma Talk". Commercial solicitations, flaming, or other disrespect of anyone on or off this list is not allowed. Please do not post chain letters or other forwarded messages that ask you to "send this to ten other people". Except for occasional on-topic forwarded announcements, posts should be original questions, comments or responses from members of the group. PLEASE REMEMBER; even though you must be a member to post, this is a public group. There are over 600 members and anyone can look at posts. If you want to keep something private, correspond privately with that person, not through postings. Let me know if you have any suggestions or comments about this group. May God be with each of you.