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04-12-2007, 07:43 PM | #1 | ||
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New Member
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Hi Everyone,
I'm Beth from the Outer Banks in NC and I have been dealing with RSD in my left foot since Dec. 06 from a MVA. I've been lurking around a few boards learning a lot about RSD and making sure I am getting the treatment I need. I just found out Monday about the Chiari I Malformation so I have been doing quite a bit of surfing the net. If anyone has any info to share that would be great. I wish all of you as pain free days as possible. Take Care, Beth Radigan |
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04-12-2007, 07:59 PM | #2 | |||
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Hello welcome to NT.
Another combo dx - so sorry about that. I hope you are able to find and get good treatment for both.
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05-19-2007, 09:07 PM | #3 | ||
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05-20-2007, 08:18 AM | #4 | ||
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Hey, Beth.
I just wrote Angela about this. Check out these sites: www.wacma.com www.ASAP.org www.chiarione.org www.conquerchiari.org Also, make sure to find a good, experienced neurosurgeon so you'll know whether you're a surgery candidate or not. A neurologist will be of no help whatsoever. Good luck! LIZARD |
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01-03-2010, 11:57 AM | #5 | ||
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I, too, am dealing with RSD like symptoms that I suffered with right after my failed surgery and now came up randomly after 8 years. I am trying to get doctors help to do an MRI because I don't know if it is the RSD itself or if something has changed in my neck to cause compression.. How can I tell??
Good luck to you and I wish you all the best! Attend conferences thru the Chiari orgs. and be informed.. NEVER have surgery unless you have done a lot of research and are fully confident in your doctors knowledge of this condition.. Believe me.. I learned the hard way!! Good luck.. ( I can't type as finger's are numb now!!) |
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