Growing hope for all with Rett Syndrome Get involved! Visit us online: Rett Syndrome has been reversed in the lab and could be one of the first childhood neurological diseases to be cured. We are hopeful Rett research could also lead the way to treatments for millions of others suffering from these types of disorders. From the moment I heard about GP2C I knew they were special. The support, the inspiration, the knowledge they have and share has been amazing. I have made wonderful friends who I know will always be there for my daughter and our family. My journey as a parent to a child with Rett Syndrome was forever changed and made easier just by being a small part of this wonderful organization’s family. I am most impressed by the way Girl Power 2 Cure has responded to the need to give Rett children powerful access to learning and experiences long held unattainable. Girl Power 2 Cure stays on the cutting edge. This is what makes the charity unique and outstanding. Aleksandra Djukic, MD, PhD. Director, Tri-State Rett Syndrome Center Associate Professor of Neurology and Pediatrics Montefiore Medical Center - Albert Einstein College of Medicine Dawn - Rett Syndrome parent Donor Resources, materials and activities for: • Rett families and their children • Therapists and Educators • Raising funds Visit our website to learn about supporting GP2C as a donor, volunteer, event host, or community outreach organizer! We need YOUR POWER to help those battling Rett Syndrome! Girl Power 2 Cure, Inc. 1417 Sadler Road #122 Fernandina Beach, FL 32034 904.277.2628 our websites: gp2c.org rettgirl.org rettuniversity.org GIRL POWER 2 CURE, INC IS A 501 (C)(3) NONPROFIT ORGANIZATION TAX ID 20-8011668
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Growing hopefor all with
Rett Syndrome
Get involved!
Visit us online:
Rett Syndrome has been reversed in the lab andcould be one of the �rst childhood neurologicaldiseases to be cured. We are hopeful Rett researchcould also lead the way to treatments for millions of others su�ering from these types of disorders.
From the moment I heard about GP2C I knew theywere special. The support, the inspiration, theknowledge they have and share has been amazing.I have made wonderful friends who I know willalways be there for my daughter and our family. My journey as a parent to a child with Rett Syndrome was forever changed and made easier just by being a small part of this wonderful organization’s family.
I am most impressed by the way Girl Power 2 Curehas responded to the need to give Rett childrenpowerful access to learning and experiences longheld unattainable. Girl Power 2 Cure stays on thecutting edge. This is what makes the charity unique and outstanding.
Aleksandra Djukic, MD, PhD.Director, Tri-State Rett Syndrome Center
Associate Professor of Neurology and PediatricsMontefiore Medical Center - Albert Einstein College of Medicine
Dawn - Rett Syndrome parent
Donor
Resources, materials and activities for:• Rett families and their children• Therapists and Educators• Raising funds
Visit our website to learn about supporting GP2C as a donor, volunteer, event host, or community outreach organizer! We need YOUR POWER to help those battling Rett Syndrome!
Girl Power 2 Cure, Inc.1417 Sadler Road #122
Fernandina Beach, FL 32034904.277.2628
our websites:gp2c.org rettgirl.orgrettuniversity.org
GIRL POWER 2 CURE, INC IS A 501 (C)(3) NONPROFIT ORGANIZATIONTAX ID 20-8011668
We educate and raise awareness because those with Rett Syndrome have the right to be heard.
Through webinars, events, and awareness campaigns, we have inspired a movement of thousands, and need thousands more.
We support families because they are the heroes, tirelessly caring for their children, siblings and grandchildren.
We open our arms to every family, meet them where they are and provide them with the resources and support they need to �ght for their children and for a cure. From helpful product reviews and hands-on training to fundraising e�orts, we walk with them on the journey that many of us have made ourselves.
We fund researchbecause the world needs these children.
They are brave, they are bright, and they are strong. We cannot rest knowing Rett Syndrome is curable. We are determined to see all those who are su�ering live better lives. Through a strong partnership with the Rett Syndrome Research Trust, we fund research that is crucial to developing treatments and a cure.
We inspire actionbecause change starts with a simple belief - that children losing the ability to walk, speak or use their hands for a lifetime is unacceptable.
www.gp2c.org
#GP2C #RiseAboveRett #HopeInAction #UntilTheyCan
Debilitating neurological disorder that primarily
a�ects females but can a�ect males.
The leading genetic cause of severe
neurological impairment in girls - most cannot
speak, walk or use their hands.
As prevalent as Cystic Fibrosis, ALS a
Huntington’s Disease.
Another child is born with Rett Syndrome
every 90 minutes.
Caused by a random X-chromosone mutation
that can strike any family, anywhere.
There are close to half a million children and
adults su�ering worldwide.
About Rett Syndrome· Rett Syndrome will be the �rst reversible
neurological disorder.
· In the unlimited potential for Rett children.
· In empowering Rett Syndrome families.
· Empathy, dignity and respect are imperative.
· Collaboration makes us better.
· In being good stewards of our resources.
· Rett Syndrome will be the �rst reversible
neurological disorder.
· In the unlimited potential for Rett children.
· In empowering Rett Syndrome families.
· Empathy, dignity and respect are imperative.
· Collaboration makes us better.
· In being good stewards of our resources.
...In living fulfilled lives today and a life without
Rett Syndrome tomorrow
We believe...
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