Is it better that I see a well known chiari specialist..for example, like one of the ones on the drs list on this site?
No worries....as for instability....yes, it can be related to Chiari in that Ehlers-Danlos is a related condition and usually the reason for instability as it is a connective tissue disorder....with the tissue that are to hold our joints in place fail, our muscles try to help causing all over joint and muscle pain.....
Do look into EDS and have it ruled out. EDS can cause Headaches, and many of the same symptoms as Chiari....
Thank you so much for your advice..I'm not gonna give up on finding answers..especially since my health is slowly deteriorating right before my eyes...and it is the most scariest thing. I'm glad I could come on here for support. Thank you.
Thank you for your response. I have not been diagnosed with chiari but I have so many similar symptoms to it. Is instability in the C1 and C2 related to chiari at all?
Push for more testing and answers....that is the way to move forward....Many Chiari specialists will offer all sorts of tests in hopes to rule out the related conditions and to help them know the best way to proceed should surgery be an option.
Hang in there.
I have been diagnosed with cranial cervical instability and chiari.. I have had the Flex extension exray only because, I was getting a second opinion and this doctor said i needed to do it, then came to find out that those exray are not for diagnosing CCI.. I also did physical therapy for my neck wich did nothing!! My dizziness is much worse my vision is worse and now I at the point I no longer go out...but I do have a good NS who did diagnos me from the very beginning when he first saw my MRI saw make sure you find a good chiari specialist..I am going to have sugery next moth the decompression and the fusion of myC1&C2... I also did a lot of research and had several second and third opinions..before I made my decision.
Good luck and keep us posted