Thank you Ashbourne an Cicina! I have been patiently letting the doctors assess and they are testing for diseases with MRI and sorting. As Rose suggested, they have, also, sent me to specialists to sort. I'll keep getting treated and see if they find consensus on a diagnosis so that I might recover.
Everyone is here to find out what is wrong with them. We need to find answers so if the doctors cant give us a diagnosis we have to find out other ways. Not everone has medical insurance that they can count on for a diagnosis, I know my HMO is not coming up with answers. What are the next best solutions
Ca2015 said:
Thank you Ashbourne an Cicina! I have been patiently letting the doctors assess and they are testing for diseases with MRI and sorting. As Rose suggested, they have, also, sent me to specialists to sort. I'll keep getting treated and see if they find consensus on a diagnosis so that I might recover.
"Gelu65" totally with you on medical insurance. But if doctors cant find I dont think there is any other way !! I know you might have to spend.
But if we have Ataxia, even after finding it is useless as there is no cure to it , only it will add to our frustration and scare.
Hope you or any one here don't come POSITIVE on this monster.
I was first diagnosed with conversion disorder, but that was changed to cerebellar ataxia. Apparently conversion disorder is very rare.
Yup I hear ya ......I am on neuro #10 ( not a typo) , soon to see #11 and #12 , along with at least a dozen and a half other specialists , therapists , and clinicians . Good luck ......