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.
Mine was Dr. Phillip Theodosopoulos at the Mayfield clinic - Cincinnati is not quite the midwest yet but it's fairly close. He and his team were excellent.
Does anyone have a really good Neurosurgeon they can recommend? Preferably in the midwest? Was diagnosed with meningioma in Sept. MRI showed 2". Doc wants
Hello-- I've been a member of this group for several years, but have not read posts most of that time. I'm resurfacing now because the meningioma continues to
Have any of you visited this site? http://www.braintumor.org/upload/contents/330/GuideFINAL2007.pdf My neurosurgeon suggests having a MRA to look at my