Guest guest Posted July 12, 1999 Report Share Posted July 12, 1999 Hi everyone. As some of you may remember, my daughter had decompression surgery January 1999 with Dr Frim. Most of her symptoms,which started during infancy (she's 6 years of age next week), disappeared after her surgery. She's still doing remarkably well with the exception of her bladder and bowel control problems, which we are trying to follow-up on. We were denied out-of-country surgery costs by OHIP (Ontario Health Insurance Plan) because Posterior Fossa Decompression surgery is a medical procedure which is insured here in Ontario (i.e., they know how to do that here). However, 3 pediatric NSGs didn't agree with the Chiari Malformation I diagnosis obtained by Drs Milhorat and Frim because Katerina showed no tonsillar herniation. However, Milhorat and Frim noticed lack of CSF flow and other anomalies. The NSGs here also had no idea what the problem was and offered nothing to help her. We are appealing the decision. I would dearly love to get e-mails from those of you who've had posterior fossa decompression surgery for ACM who had tonsillar herniation of LESS than 5mm. If you could briefly describe your pre-op symptoms, your diagnosis and any success post-op, I would be very grateful. We are appealing in writing and must submit all relevant documentation to back our case. Thanks very much. Eurico ------------------------------------------------------------------------ eGroups.com home: /group/chiari - Simplifying group communications Quote Link to comment Share on other sites More sharing options...
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