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meningioma · Meningioma Support and Information

Group Information

  • Members: 580
  • Category: Support
  • Founded: Sep 12, 2001
  • Language: English
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Activity within 7 days:

2 New Members - 4 New Messages - New Questions

Description

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.

Most Recent Messages

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Re: I was just diagnosed with a 6mm meingiom on my 5th cranial nerve
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
Posted - Sat Nov 21, 2009 1:29 am
sylvano CERNIGLIA
straycatvano
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Re: I was just diagnosed with a 6mm meingiom on my 5th cranial nerve
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
Posted - Sat Nov 21, 2009 12:18 am
Norma Stephens
wvmtlady
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Re: I was just diagnosed with a 6mm meingiom on my 5th cranial nerve
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"
Posted - Fri Nov 20, 2009 9:54 pm
sylvano CERNIGLIA
straycatvano
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I was just diagnosed with a 6mm meingiom on my 5th cranial nerve.
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
Posted - Fri Nov 20, 2009 8:59 pm
Judy Houbre
judyhoubre
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Re: Trigeminal Neuropathy
Hello Annette,    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
Posted - Mon Nov 9, 2009 6:30 pm
Meg Kolodick
meg_kolodick
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Message History

Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec
2009 75 224 55 94 131 66 43 58 67 30 11
2008 50 74 104 37 138 111 33 100 80 102 43 87
2007 91 81 62 69 33 53 25 21 61 86 104 15
2006 70 135 152 95 60 136 261 155 213 63 150 36
2005 82 43 94 57 140 78 122 179 122 167 182 157
2004 41 70 64 20 20 23 31 30 19 38 53 75
2003 111 77 116 111 39 67 30 47 69 74 91 127
2002 1 3 15 8 15 21 8 58 67 72 44
2001 4 1 6
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