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    • Home
    • Information
    • Fibrous Dysplasia
    • McCune Albright Syndrome
    • Partners
    • Resources/Links
    • FD/MAS Stories
    • Podcast
  • Home
  • Information
  • Fibrous Dysplasia
  • McCune Albright Syndrome
  • Partners
  • Resources/Links
  • FD/MAS Stories
  • Podcast

FD/MAS Spotlight

Laura Cowell

Laura Cowell

Laura Cowell

As I sat in the neurosurgeons office I could feel my anxiety rising as I saw him bring up google to find out more. Gee, I thought, I can tell him more than google can.

Read Laura's Story

Alicia

Laura Cowell

Laura Cowell

During a heavy snowfall in Orange over 7 years ago, I started to have this constant headache along with vertigo at the time that would not subside

Read Alicia's Story

Haley

Laura Cowell

Summer

Haley is Summer's (who is living with Fibrous Dysplasia/McCune-Albright Syndrome ) sister, is her support and advocate,  

Read Haley's story

Summer

If you would like to have the spotlight on your story please reach out!

Summer

 I was diagnosed with McCune Albright Syndrome in 2014 after a lengthy period of time attending doctors with various ailments. I play social volleyball every Sunday, and this one night I was mid-game and all of a sudden, I just collapsed like my foot had given out on me.  

Read Summer's story

If you would like to have the spotlight on your story please reach out!

If you would like to have the spotlight on your story please reach out!

If you would like to have the spotlight on your story please reach out!

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