• Specifically Named Diseases

• 1.

HEMOCHROMATOSIS INFORMATION SOCIETY

The Hemochromatosis Information Society is a nonprofit organization providing valuable information to patients and physicians concerning hereditary hemochromatosis.

• Single Organization Support

• 2.

M-CM NETWORK

Improving the lives of individuals with macrocephaly-capillary malformation syndrome.

• Specifically Named Diseases Research

• 3.

GRACE SCIENCE FOUNDATION

We are changing how scientific research is done.

Foxg1 Research Foundation

FOXG1 syndrome is a childhood neurological genetic disorder and is a key to understanding many brain disorders.

• Birth Defects, Genetic Diseases

• 5.

The PolG Foundation

The mission of The POLG Foundation is to support and accelerate research to find effective treatments and a cure for PolG mitochondrial disorders.

• Fund Raising and/or Fund Distribution

• 6.

LOVE LIKE CRAZY FOUNDATION

Love Like Crazy Foundation loves families, shares knowledge about and supports research of mitochondrial disease, especially Pearson Syndrome.

• Specifically Named Diseases

• 7.

Smith-Kingsmore Syndrome Foundation

Smith-Kingsmore Syndrome is a rare genetic disease.

• Birth Defects, Genetic Diseases

• 8.

Mitchell and Friends Foundation

To raise awareness of Mitchell Syndrome and support research into possible treatments and cures Raising awareness of Mitchell Syndrome and supporting families and children with this rare neurological disease.

• Fund Raising and/or Fund Distribution

• 9.

THE CHAMP FOUNDATION

Mission The Champ Foundation supports research toward better treatment and a cure for single largescale mitochondrial deletion syndromes SLSMDS like Pearson syndrome.