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solo walks

Julie Milam

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Become a Solo Walker

It’s been 18 months since my shocking diagnosis of a rare brain disorder called Chiari. I had never heard the words Chiari or Syringomyelia before my diagnosis, but I am confident that God never gives us more than we can handle. Here’s to all the warriors facing challenges big and small, especially those no one knows about.

Please help me support the Bobby Jones Chiari & Syringomyelia Foundation by making a donation through my page. The process is fast, easy and secure. Thanks so much for your support... and please don't forget to send this page to any friends you think might be interested in donating!

Bobby Jones CSF Mission

To advance knowledge through research and to educate the medical, allied sciences and lay community about Chiari malformation, syringomyelia and related disorders

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