Home of Addi & Cassi Hempel, twins with the rare and fatal disease call Niemann Pick Type-C sometimes referred to as "Childhood Alzheimer's". The most exhaustive collection of information and resources about research into this deadly c
The Quinn Madeleine Foundation's mission is to promote and support research on treatments and a cure for Niemann-Pick Disease, Type A, and to facilitate memorable experiences for young children with life-limiting illness and their families.
Home of Addi & Cassi Hempel, twins with the rare and fatal disease call Niemann Pick Type-C sometimes referred to as "Childhood Alzheimer's". The most exhaustive collection of information and resources about research into this deadly c
Home of Addi & Cassi Hempel, twins with the rare and fatal disease call Niemann Pick Type-C sometimes referred to as "Childhood Alzheimer's". The most exhaustive collection of information and resources about research into this deadly c
Home of Addi & Cassi Hempel, twins with the rare and fatal disease call Niemann Pick Type-C sometimes referred to as "Childhood Alzheimer's". The most exhaustive collection of information and resources about research into this deadly c
Niemann-Pick Type C Disease (NPC) simply put is FATAL. It is a genetic , neurodegenerative disorder storing cholesterol within the brain, liver, and spleen.
Niemann-Pick Type C Disease (NPC) simply put is FATAL. It is a genetic , neurodegenerative disorder storing cholesterol within the brain, liver, and spleen.
The Quinn Madeleine Foundation's mission is to promote and support research on treatments and a cure for Niemann-Pick Disease, Type A, and to facilitate memorable experiences for young children with life-limiting illness and their families.
The Quinn Madeleine Foundation's mission is to promote and support research on treatments and a cure for Niemann-Pick Disease, Type A, and to facilitate memorable experiences for young children with life-limiting illness and their families.
The Quinn Madeleine Foundation's mission is to promote and support research on treatments and a cure for Niemann-Pick Disease, Type A, and to facilitate memorable experiences for young children with life-limiting illness and their families.
Niemann-Pick Childrens Fund, Inc. was organized in December of 2008 in order to raise awareness of Niemann-Pick Disease Type C and its affect on families in
The Quinn Madeleine Foundation's mission is to promote and support research on treatments and a cure for Niemann-Pick Disease, Type A, and to facilitate memorable experiences for young children with life-limiting illness and their families.
The Quinn Madeleine Foundation's mission is to promote and support research on treatments and a cure for Niemann-Pick Disease, Type A, and to facilitate memorable experiences for young children with life-limiting illness and their families.
Trent and Julie Smith started the BReaK Thru Fund in honor of their three children diagnosed with Niemann-Pick Disease Type C. The funds raised will go to research for a cure.
The International Niemann-Pick rare disease registry (INPDR) is a desperately needed collaboration between clinicians, scientists, researchers and patient associations to collect clinical, genetic, diagnostic and outcome data on patients with NPD type A,
Michael G. Stults is a leader, manager, and most importantly a team builder. He has realized that his success in his personal and business life has been
Niemann-Pick disease is an inherited condition involving lipid metabolism, which is the breakdown, transport, and use of fats and cholesterol in the body. In
Michael G. Stults is a leader, manager, and most importantly a team builder. He has realized that his success in his personal and business life has been