Yet Another Bulletin Board

Welcome, Guest. Please Login or Register.
Nov 23rd, 2024, 8:13am

Home Home Help Help Search Search Members Members Member Map Member Map Login Login Register Register
Clusterheadaches.com Message Board « Chiari Malformation - Firsthand experience/Insight »


   Clusterheadaches.com Message Board
   Cluster Headache Help and Support
   Cluster Headache Specific
(Moderator: DJ)
   Chiari Malformation - Firsthand experience/Insight
« Previous topic | Next topic »
Pages: 1  Reply Reply Notify of replies Notify of replies Send Topic Send Topic Print Print
   Author  Topic: Chiari Malformation - Firsthand experience/Insight  (Read 759 times)
Mikella
New Board Newbie
Canada 
*




I love YaBB 1G - SP1!

   


Gender: female
Posts: 50
Chiari Malformation - Firsthand experience/Insight
« on: Oct 22nd, 2007, 12:23pm »
Quote Quote Modify Modify

Just as the title says, I'm wondering if anybody here has/had a chiari malformation. Putting it out there, then I'll ask questions. Anybody have experience with them? Somehow know a lot about them? Because I have scoliosis (my spine is a backwards "S", luckily you can't really tell......) and have had severe severe neck problems, this is a real possibility......... (not going to get into all of the symptoms, no need). There is something (scary) structurally wrong with my neck I've been told (and know), but nobody has figured it out yet. If this is the case, it would explain the mind-blowing pressure in my head (it would be the build-up of cerebrospinal fluid) and all the other chiari malformation/cluster symptoms etcetcetc (some different, some the same). I'm also losing use of half of my right hand, which is the same side as the root of all my neck problems, the base of my skull on the right side. Not sure if this would be causing the "cluster" pain/symptoms, or if I may have both (which I think may be the most likely whereas I don't THINK a chiari malformation would explain the autonomic symptoms etc). This definitely makes sense, so I'm just looking for real insight. I don't know what to do until my appointments...... my next neuro appt. isn't until Dec. 4th.. I NEED an MRI. I've never had one for any of this. It feels like if I put a needle into my head, it would just pop.  Shocked
 
Thanks for any info <3
 
IP Logged

"Know how sublime a thing it is.. to suffer and be strong" HWL
Pages: 1  Reply Reply Notify of replies Notify of replies Send Topic Send Topic Print Print

« Previous topic | Next topic »


Clusterheadaches.com Message Board » Powered by YaBB 1 Gold - SP 1.3.1!
YaBB © 2000-2003. All Rights Reserved.


©1998-2010 Web Vision Enterprises All rights reserved. All information on this site is protected by international copyright laws. You may not re-distribute any information from this site without written permission from Web Vision Enterprises and the webmaster of this site. Violators will be prosecuted.
You may view our privacy policy and financial disclosure statement here

test rss