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Miles

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Hello Group,

This is the first time I have written. My son Miles is 15 and diagnosed with

ACM and SM on June 13. We moved very quickly since summer was just beginning

and I am a teacher, and his decompression surgery was done on June 19. He is

now 3 weeks post-op and doing well. He does not have as much energy as he

did before surgery, but the neck pain he was suffering from is gone. He

still complains about the muscles in his neck hurting, which I assume is

from the surgery, and an occasional headache, but nothing like before.

We return to the NSG on July 26 for an MRI to see about the SM since the

surgery. Of course we are all hopeful it will have dissapated, but are

waiting to see. I am interested in others who have SM and the outcomes of

procedures you have been through.

Thanks for being there,

Debbie

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