I really have to praise all the people who have carried the basic topics on this Forum from the old forum. When you were all together you left a trail of information that has allowed others to read, study and look at their spine problems from multiple prospectives. I congratulate you.
Carol, in one of your posts you were speaking to "Vic". The subject was Spondy.
You stated "I forgot to mention that I too heard that the spine institutes generally don't touch cases of spondy...so I did ask LSI representative, his response was that the doctors @ LSI and the MRI results both did not indicate spondy and if my neurosurgical consult and second opinions did, it was probably to as a cautionary/scare disclaimer to cover bases and confirm their reason for their recommendation of fusion."
Did none of your surgical consults not take and X-Ray to confirm your spondy?
I did not have spondy according to my MRI. It was not until 7 months later after Pain Management injections and my first surgical consult that I learned of having spondy. The orthopedic surgeon took an X-Ray for confirmation. That is what he showed to me.
Later, talking to my PM, I was told an MRI evaluates soft tissues and not bone tissue. Only X-Ray determines the state of the vertebrae. His opinion was that it (the spondy)was not severe enough to cause pain, but he did refer me to another surgeon.
From your post, I am assuming when you sent "stuff" to the Spine Institutes in Florida, no X-Ray or written report on that X-Ray was sent to them.
Is my understanding of your experience correct?
I know when I was told that I had spondy, I was ticked, expecially when the MRI specifically stated, "No spondy seen."
I think what holds us backfrom spinal surgery might not just be $$$$ but our concern about spondy. What does it hold for us now and in the future; that is the big question.
DMB