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.
Congrads on that new baby .He will make you feel a lot better. Good luck with the blood mess. i thought brain surgery is the littlest blood loss of all
Hey Mrio, I have that memory loss thing also, but I tell folks it's oldtimers syndrome. The thing that bothers me most is the random phantom smells...I smell
Bless you all!! I am home but I have to go Monday for blood work so they can try to type my blood.AGAIN!! Apparently, the blood I was given for my brain