Girl Power 2 Cure, Inc. is a 501c3 nonprofit organization dedicated to raising awareness and funds for treatments and a cure for Rett Syndrome, a devastating neurological disorder that almost exclusively affects girls.
We are committed to making Rett S
Girl Power 2 Cure, Inc. is a 501c3 nonprofit organization dedicated to raising awareness and funds for treatments and a cure for Rett Syndrome, a devastating neurological disorder that almost exclusively affects girls.
We are committed to making Rett S
Mikyla-Cure is a 501(c)3 non-profit organization that was founded by Robert and Annie Smith. Its goal is to raise funding for research into a cure for Rett Syndrome, a neurodevelopmental disorder that his daughter Mikyla has. Joining the effort is Scott P
The Rett Syndrome Research Trust is a non-profit exclusively devoted to global research on Rett Syndrome and related MECP2 disorders. Our goal is to heal
The Rett Syndrome Research Trust is a non-profit exclusively devoted to global research on Rett Syndrome and related MECP2 disorders. Our goal is to heal
l’Association Française du Syndrome de Rett a pour objectifs de soutenir les familles, faire connaître la maladie, promouvoir la recherche et agir pour la reconnaissance du citoyen polyhandicapé au sein de la collectivité nationale
Girl Power 2 Cure, Inc. is a 501c3 nonprofit organization dedicated to raising awareness and funds for treatments and a cure for Rett Syndrome, a devastating neurological disorder that almost exclusively affects girls.
We are committed to making Rett S
Girl Power 2 Cure, Inc. is a 501c3 nonprofit organization dedicated to raising awareness and funds for treatments and a cure for Rett Syndrome, a devastating neurological disorder that almost exclusively affects girls.
We are committed to making Rett S
The Rett Syndrome Research Trust is a non-profit exclusively devoted to global research on Rett Syndrome and related MECP2 disorders. Our goal is to heal
The Rett Syndrome Research Trust is a non-profit exclusively devoted to global research on Rett Syndrome and related MECP2 disorders. Our goal is to heal
The Rett Syndrome Research Trust is a non-profit exclusively devoted to global research on Rett Syndrome and related MECP2 disorders. Our goal is to heal
The Rett Syndrome Research Trust is a non-profit exclusively devoted to global research on Rett Syndrome and related MECP2 disorders. Our goal is to heal children and adults who will otherwise suffer the effects of these disorders for the rest of their li
curerett.org is a charity created to raise awareness and funds to cure Rett syndrome, a neurological condition that affects girls from 6 months old, affecting every aspect of life; speaking, walking, eating and even breathing.
This is our beautiful daughter Esmé. In October 2013 when she was almost 3.5 years old, we were given the life-changing news that she has a rare neurological condition called Rett Syndrome. We felt completely crushed and devastated by this news. The futur
curerett.org is a charity created to raise awareness and funds to cure Rett syndrome, a neurological condition that affects girls from 6 months old, affecting every aspect of life; speaking, walking, eating and even breathing.
curerett.org is a charity created to raise awareness and funds to cure Rett syndrome, a neurological condition that affects girls from 6 months old, affecting every aspect of life; speaking, walking, eating and even breathing.
curerett.org is a charity created to raise awareness and funds to cure Rett syndrome, a neurological condition that affects girls from 6 months old, affecting every aspect of life; speaking, walking, eating and even breathing.
curerett.org is a charity created to raise awareness and funds to cure Rett syndrome, a neurological condition that affects girls from 6 months old, affecting every aspect of life; speaking, walking, eating and even breathing.
my Dad is running the 2016 Boston Marathon in April to raise money for Rett Syndrome trials going on there now at Boston Childrens Hospital and MIT. Most of you know I have Rett Syndrome. So this is so important that we keep the research moving and at a f
Blue Olive was formed out of a need for supportive merchandise for people with special needs. We are proud of the special needs community and only offer shirts with encouraging messages. Blue Olive also works with missionaries and non-profits to raise f