
PMD Foundation
#Research #Awareness #Advocacy & #FamilySupport for those with #PelizaeusMerzbacherDisease #PMD #newbornscreening #raredisease #leukodystrophy #myelin The PMD Foundation is a 501(c)3 non-profit organization formed to serve three distinct interest groups as they relate to Pelizaeus-Merzbacher Disease: The Children and Families, the General Public, the Researchers and Clinicians.
522336287
EIN
Marlton, NJ 08053 USA
Address
pmdfoundation.org
Web
_pmdfoundation
Twitter (116)
ThePmdFoundation
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Were collecting stories of families and people living with PMD PMLD. The PMD Foundation serves those affected by PMD through education research service and advocacy. Access our resources for families Share your story join our community view helpful information and much more. Were on the cutting edge of research Governments associations and scientists regularly access our repository of research.
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