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Daughter's nsg apt.-LONG

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Hi everyone.I've been reading the postings for a few weeks now and

finally decided to write you about my daughter. Her name is Cassy and

she has had multiple medical problems since birth. She is now 16 and ACM

is just the latest in this long story.She was first diagnosed with ACMI

in November of 1995 when an MRI was done because she was having

headaches.The doctor didn't propose that anything be done at that time.

Since last fall she's been having headaches every morning and the

headaches started increasing in December along with a host of other

symptoms.She has dizziness,nausea,fatigue,neck and head pain,etc.etc.

Most recently she has had difficulty swallowing and has had numbness and

tingling in her right arm along with some decreased pain sensation in

her hands. She went to see a neurologist on Jan.27 and I felt like he

pretty much blew us off.He said Chiari I was usually asymptomatic and

that her neurological exam was normal.I was referred to him by my

daughter's orthopedist since she had been seeing him for another

problem. He was quite concerned when he saw she had been diagnosed with

ACMI and got us in to see the neurologist within a week so I was

surprised at the neurologist's reaction. She had another MRI done

however and this showed that a syrinx has developed.She is scheduled to

see a neurosurgeon on Feb.22 and I'm hoping this guy has a different

attitude.My question is can you guys give me some advice on what to ask

the nsg and how likely do you think it is that they will operate based

on her condition now? Sorry this is so long.

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