What does RSRT mean in SYNDROMES
Rett Syndrome Research Trust (RSRT) is a charitable organization dedicated to the research, diagnosis and treatment of Rett syndrome. Established in 2004, this non-profit has helped advance the field of Rett syndrome research and provided invaluable resources to families affected by the disorder. Through their generous support, they are working towards improving quality of life for individuals with Rett syndrome and their families. By raising awareness, educating medical professionals and providing financial support, RSRT is making a significant difference and paving the way for life-changing breakthroughs in testing, treatments and cures.
RSRT meaning in Syndromes in Medical
RSRT mostly used in an acronym Syndromes in Category Medical that means Rett Syndrome Research Trust
Shorthand: RSRT,
Full Form: Rett Syndrome Research Trust
For more information of "Rett Syndrome Research Trust", see the section below.
What is Rett Syndrome
Rett Syndrome (RTT) is a rare neurodevelopmental disorder that primarily affects girls and is characterized by progressive loss of muscle control, communication difficulties, intellectual disability, seizures, motor deficits and sensory problems. The majority of children diagnosed with RTT experience a period of developmental regression between ages 6 months to 1 year where they lose language skills they had previously acquired as well as other abilities including purposeful use of hands. They may also exhibit autistic behaviors such as repetitive hand movements. Currently there is no known cure or effective treatment for RTT; however early diagnosis increases chances of better outcomes.
The Role of RSRT
The mission of RSRT is to fund innovative research programs that will help unlock potential treatments for RTT in hopes for a brighter future for individuals with the disorder. In addition to funding cutting-edge research from all over the word, they provide educational tools, emotional support services and family grants that further their commitment to supporting those affected by RTT. Thanks to the work done through the organization's website, newsletter and social media channels they have been creating awareness about RTT which can lead to earlier detection giving them an even greater opportunity at improving quality of life. Through their philanthropy efforts with both monetary donations as well as volunteerism; meaningful progress continues in finding treatments or ultimately discovering a cure for RTT.
Essential Questions and Answers on Rett Syndrome Research Trust in "MEDICAL»SYNDROMES"
What is the Rett Syndrome Research Trust?
The Rett Syndrome Research Trust (RSRT) is a non-profit organization dedicated to finding treatments, and ultimately a cure, for Rett syndrome through research. Since 2007, RSRT has contributed more than $36 million in grants to researchers around the world working on studies that explore the biology of Rett syndrome, develop and test potential treatments, and further our understanding of this disorder.
How does the Rett Syndrome Research Trust fund research?
The RSRT funds research through two primary initiative areas: Innovative Research Grants program and Scientific Collaboratives program. Through these programs, qualified researchers can submit applications requesting funding for specific projects related to improving the lives of individuals with Rett syndrome. All applications are carefully reviewed by our scientific review committee made up of experts in the field of Rett syndrome before any grants are awarded.
Is there any other way I can support the work of the Rett Syndrome Research Trust?
Yes! You can make donations directly to us or become a fundraising ambassador to help raise awareness and funds for our initiatives. Additionally, you can also join one of our community events such as virtual educational seminars and online donation drives. Any support you can provide will go a long way towards helping us reach our goals.
How much money has been raised by the RSRT since it began?
The RSST has raised over $36 million since it began in 2007. These funds have been used to support multiple types of research projects related to improving outcomes for individuals living with Rett syndrome.
What types of research projects is RSST funding?
We fund a variety of different types of research projects ranging from basic scientific studies exploring biological mechanisms underlying disease symptoms, preclinical testing to determine safety and efficacy of potential treatments, clinical trials assessing whether new therapies are safe and effective for use in people with this condition, epidemiology studies aimed at better understanding prevalence and patterns among affected individuals, as well as educational webinars helping families better understand their diagnosis.
Who reviews grant applications submitted to RSST?
Applications are carefully reviewed by experts from scientific review committee made up medical professionals who have experience with or knowledge about this disorder before any grants are awarded. This ensures that all applications get fair consideration for funding.
Does RSST only provide financial support or do they offer other forms of assistance?
In addition to providing financial assistance through grant programs, we also offer additional resources such as professional advice from specialized physicians/experts in this field as well as informational materials such as patient/ family guides designed to help those affected by this condition better manage their everyday lives.