• Private Grantmaking Foundations

• 208.

Jain Foundation Inc

The Jain Foundation's mission is to identify treatments for Dysferlinopathy also known as LGMD2B/R2 or Miyoshi Myopathy ORCHESTRATING A CURE FOR DYSFERLINOPATHY The Jain Foundation is singularly focused on finding a cure for dysferlinopathy also referred to as LGMD2B LGMDR2 Miyoshi Myopathy 1 ORCHESTRATINGA CURE FORDYSFERLINOPATHY The Jain Foundation is singularly focused on finding a cure for dysferlinopathy also referred to as LGMD2B LGMDR2 Miyoshi Myopathy 1 WHAT IS DYSFERLINOPATHY.

PROPIONIC ACIDEMIA FOUNDATION

Finding better treatments and a cure for Propionic Acidemia since 2003 The Propionic Acidemia Foundation is a 501(c)3 non-profit organization dedicated to finding improved treatments and a cure for Propionic Acidemia by funding research and providing information and support to families and medical professionals.

• Alliance/Advocacy Organizations

• 210.

Trpm3 Foundation

Patient advocacy and support for those affected by #TRPM3 #ionchannel related disorders.

• Public Health Programs

• 211.

Energy and Living Inc

Our mission is to help people with chronic fatigue syndrome , known as ME/CFS, make lifestyle changes, recover and re-integrate into the society.

• Adult, Continuing Ed

• 212.

Society for Muscle Biology Inc

Society for Muscle Biology official twitter account.

• Fund Raising and/or Fund Distribution

• 213.

Save the Mommies Inc

Early DiagnosisSaves Lives Prevention of Peripartum Cardiomyopathy Project.

• Medical Specialty Research

• 214.

Curemapk8Ip3 Foundation

Family support network for patients and their families affected by a gene mutation in MAPK8IP3 Page for individuals and families with gene variant MAPK8IP3 Improve the lives of patients and families affected by a MAPK8IP3 gene mutation by performing the following activities: raising community awareness of MAPK8IP3-Related Neurodevelopmental Disorder; facilitating research of MAPK8IP3-Related Neurodevelopmental and related Disorders; collecting and disseminating information and resources relating to MAPK8IP3-Related Neurodevelopmental and related Disorders; supporting those affected by MAPK8IP3-Related Neurodevelopmental and related Disorders; and any other charitable educational or scientific activities that are in furtherance of the Corporation's purposes.

• Nerve, Muscle, and Bone Research

• 215.

THE MPN RESEARCH FOUNDATION

We’re a global research foundation stimulating research in pursuit of new treatments, & eventually a cure, for PV, ET, & MF.

• Nerve, Muscle, and Bone Research

• 216.

GIVING STRENGTH INC

Every dollar raised and donation made will make a major impact on future research for congenital muscular dystrophy subtype, SELENON.