Translate This Page With Yahoo Babel Fish
<p>Donate To FNMS</p>
The Foundation for Nager and Miller Syndromes

Welcome to FNMS Online

The Foundation for Nager & Miller Syndromes

Founded in 1989 by Margaret Hogan as a self-help/support group & network of families affected by either Nager or Miller Syndromes, Margaret’s mission continues today to help FNMS members go from surviving to thriving through the sharing of experiences and information!  If you or a loved one has either of these syndromes and would like to join us as an FNMS Family or Individual Member, contact us via our contact page.
Nager And Miller Syndromes
Photo Gallery
Blog
Calendar of Events
Multi Media
Nager And Miller Syndromes
  • <p>FNMS Image 1</p>
  • <p>FNMS Image 2</p>
  • <p>FNMS Image 3</p>
  • <p>FNMS Image 4</p>
  • <p>FNMS Image 5</p>
  • <p>FNMS Image 6</p>
  • <p>FNMS Image 7</p>
  • <p>FNMS Image 8</p>
  • <p>FNMS Image 9</p>
  • <p>FNMS Image 10</p>
  • <p>FNMS Image 11</p>
  • <p>FNMS Image 13</p>
Nager And Miller Syndromes Nager And Miller Syndromes

Winter 2022

Newsletter

is now online!

/uploads/pdf/winter2022webversionfnmsnewsletter.pdf

2023 FNMS Family Conference Colorado Springs, CO

Our Conference Date has moved!  The 2023 FNMS Conference will be held August 3 - 6, in Colorado Springs, Colorado.  The registration form and current details will be emailed out to all FNMS Member families this week!   




 
news
Oct 23		 FNMS Angel Gabriel Revis
Heaven has gained yet another FNMS Angel. We are truly heartbroken to announce the passing of Gabriel Revis. Gabriel was for a brief time, an Angel here on Earth. His smile could light up an entire building and he touched hundreds, perhaps thousands o read more
 

Newsletter Sign Up

Sign up to recieve our newsletter!