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Mitzie

I am sorry for your pain and suffering, my son is 10 and has chiari...it is a

long hard fight as everyone on this group knows. My son is 4-5 mm which isnt

really considered chiari to a neruologist or a regular pcp that doesnt know

anything about chiari. but my son has had problems since the age of about 3.

finally his grandmother found out she had chiari and then thats when we began

wondering and after test and fights with dr's all three of my kids have it as

well as my husband. my son is the only one that has gone for surgery so far

other then his grandmother. and just know that you are going to a wonderful dr.

he did her surgery and did a wonderful job.

his partner who is Dr. Jimenez did kylers and he is such a wonderful dr also. I

will keep you in my prayers and wish you luck!! I feel that you will get answers

when you see Dr. Oro

hugs and prayers

angie

mitziekennedy wrote: Hi! My name is Mitzie and I am

28. I found out a month or so ago

that I have chiari. I live outside Oklahoma City. The neurosurgen

told me they couldn't do anything for me at this time. He told me to

go back to my neurologist, neurologist said he couldn't do anything

and told me to goto my family doctor for pain meds (he can say chiari

he just spells it to me). I have been sick for about 10 years. None

of my doctors have told me anything chiari. What I have learned has

been from the web. I just got a copy of my MRI and report today. I

am 5mm on right side and 2mm on the left. Ok to my question... Is

5mm bad? I can't seem to find out what is an okay range. The report

says I am only borderline chiari. What is borderline and what is

not? Thank you for any help. I will be attending the conferance

this weekend. I have an appointment to see Dr. Oro in November. I

hope this weekend I can get some questions answered because no doctor

in Oklahoma seems to know anything.

Thank You,

Mitzie in OK

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