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Hey Ginger and group!

I hate when I see statistics like that 20%.Sure it's

scary!I have a syrinx.I was told by 3 nsg's it was

gone.Now Dr.Paschall says it is very much there.It's

shriveled.So does that put me in that % thing?Probably

not.

I was born with acm and it went undetected until I

was 41.I was a clumsy kid.I remember crying in pain

and Mom saying it was growing pains.I stunk at sports.

Cody was detected and treated early.That's a

plus.From what you write about him he's a tough kid.I

live each day to the fullest.One just never knows.

Sometimes when I read some of the posts I wonder

should I stay ignorant to my disease.Not!Some things

are disturbing.What we have is real!We also have each

other.That's the miracle.

I have been looking into syringomylia,not finding

much on shriveled syrinx though.Any info would be

appreciated.Much love to all!

Hugs,

Lee

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