This group is associated with the "Meningioma Support and Information" web site. I have not kept the links in it up-to-date, but it can be a starting point to research more information on meningiomas.
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". If you are familiar with the MSN style group and would prefer that format, visit "MSN group Meningioma".
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. Let me know if you have any suggestions or comments about this group. May God be with each of you.
My "M" right infra tempra fossa 2 CM could have been there for years. It was not causing any symptoms and would not have been found if I didnt have a cat scan
Hey Judy! Welcome! Just take a deep breath and relax. Don't panic. That makes the whole nervous system work overtime and your body reacts with twitches and
Well to start with with You are in the right place. There is no need to panic at this stage. The people in this room will give an honest information. My "M"
Hi all, I am new to this group and just was diagnoesed with a 6mm meningioma on my 5th cranial nerve it started with a twitch in my lip my GP said it was
Hello Annette, Â Â 6 years is a terribly long time to be in so much pain! What have your doctors done to try to find a cause for it? I was having severe pain