Chiari Malformation - Online Support Group
We are patients and survivors of Chiari (types I-IV), here for your support.
I noticed that there were no groups at all on our site. I also realized recently that I would personally benefit from chatting with other Chiarians that are local for me. I am still looking for a NS, and interested in hearing about local providers that you may have seen. When I searched to see who is in CA on the site, there were several. A couple even pretty close to me!
Join me in forming a Californian Chiarian Group so that we can share information specific to our State! Send me a friend request if you would like an invite!!!
Thank you,
Lisa
Started by Lisa. Last reply by Sandy May 5. 18 Replies 0 Likes
Hi There! I am starting to compile a list of Neurologists and Neurosurgeons I have found so far in California that have at least some level of 'expertise' in ACM. Please note that the only Dr. on…Continue
Started by Lisa Jan 20, 2011. 0 Replies 0 Likes
Conquer Chiari WebsiteConquer Chiari recommends that anyone diagnosed with Chiari be evaluated by a…Continue
Started by Lisa Jan 17, 2011. 0 Replies 0 Likes
WACMA Site List of Dr. QuestionsThings to discuss with your doctor BEFORE surgery 1. How many ADULT ACM Patients have you seen? (change this to…Continue
Started by Lisa. Last reply by Lisa Jan 17, 2011. 2 Replies 0 Likes
I have found some other Chiari 'experts' (I use that term loosely as this condition is still not that well understood), that are relatively nearby to California but would require travel out of…Continue
Comment
Comment by Sheila on April 5, 2012 at 11:00pm
Comment by Jenny Foulk on March 30, 2012 at 11:07am Hey everyone! I will be hosting the first ever Nor Cal CCWAA here in Sacramento this September! I would love to meet anyone in the area and hope to have your support in the walk! Also, I don't know a single person with Chiari in "real life" so I hope to meet some of you Sacramento-area people!
Comment by Sheila on March 25, 2012 at 10:13pm I live in Redding but I was in Sacramento for few years. I travel back every month as my family still lives there. I would love to meet you and your daughter. I hope to be back in Sac in the next few weeks, let me know what works best for you. I was diagnosed in 2008 but have suffered for more than 25 years.
Comment by Megan's Mom on March 25, 2012 at 3:03pm Is there anyone up in the Sacramento valley. My daughter is looking to meet more people who have Chiari.
Comment by Megan's Mom on February 23, 2012 at 2:33pm I am up here in Sacramento. The NS that my daughter has is a very good NS. He is very good at what he does, he helps you understand what is going on.
Comment by hartnsoull on February 10, 2012 at 7:40pm Hi. Im from Hanford California. Is there anyone remotely close to hanford? Is fibromyalgia common diagnosis with any of you guys?
Hello all, I am new to the group and glad to found this sub-group. I live in San Gabriel Valley, would love to learn others in southern california on which NS you see.
Comment by Jennifer Dorkin on April 26, 2011 at 11:26pm UPDATE! I was approved as the Southern California Rep for CCWAA and the walk will be held in September, in Irvine! Please join us! Tell everyone you know, get people to sponsor you! Use it as a chance to raise awareness with your friends, family and acquaintances. Come walk with us, volunteer if you can, donate or ask others to donate to this awesome cause that supports patient education and research into Conquering Chiari!
Click below to register today!
Comment by Jennifer Dorkin on February 19, 2011 at 1:30am Hello! Where in California do all of you live? I am in Orange County. I am interested in organizing a Conquering Chiari Walk Across America here in Southern California this year. I have also been trying to get a local meet-up going for people in our area with Chiari. If you are interested in helping with either one, please let me know! :)
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