Difference between revisions of "Team:New York City/Integrated Practices"

Revision as of 21:53, 12 October 2018

Integrated Practices

Huntington’s disease (HD) is a rare and deadly inherited disease, so our team was motivated to develop a cure that would attack the root of the problem instead of solely relieving the symptoms. The severity of the symptoms, along with the late onset of the disease, affects victims both mentally and physically. Thus, we wanted to spread awareness of HD and our research to both the public and scientific community. We held information sessions within our respective high schools to educate students on HD as well as our ongoing research. We also participated in New York City and Long Island Teams Hope Walk of HDSA (Huntington’s Disease Society of America) to raise awareness about Huntingtin Diease in public parks along the Hudson River and Long Island park. We also became a member of HDSA National Youth Alliance where we connected with other high school and college students who care about Huntington disease and participated in their 2019 annual fundraising and event organizing committee meetings and conference calls. Through direct outreach to institutions and educational communities such as our schools, the colleges/universities in our city, and affiliated organizations, we hoped to inspire further experimentation and interest in HD.

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-     <p class="lead">Huntington's disease (HD) is a rare and deadly inherited disease, so our team was motivated to
+     <p class="lead">Huntington’s disease (HD) is a rare and deadly inherited disease, so our team was motivated to develop a cure that would attack the root of the problem instead of solely relieving the symptoms. The severity of the symptoms, along with the late onset of the disease, affects victims both mentally and physically. Thus, we wanted to spread awareness of HD and our research to both the public and scientific community. We held information sessions within our respective high schools to educate students on HD as well as our ongoing research. We also participated in New York City and Long Island Teams Hope Walk of HDSA (Huntington’s Disease Society of America) to raise awareness about Huntingtin Diease in public parks along the Hudson River and Long Island park. We also became a member of HDSA National Youth Alliance where we connected with other high school and college students who care about Huntington disease and participated in their 2019 annual fundraising and event organizing committee meetings and conference calls. Through direct outreach to institutions and educational communities such as our schools, the colleges/universities in our city, and affiliated organizations, we hoped to inspire further experimentation and interest in HD.
-        develop a cure that would attack the root of the problem instead of solely relieving the symptoms. The
+</p>
-        severity of the symptoms, along with the late onset of the disease, affects victims both mentally and
-        physically. Thus, we wanted to spread awareness of HD and our research to both the public and scientific
-        community. We held information sessions within our respective high schools to educate students on HD as
-        well as our ongoing research. We also visited organizations like the HDSA (Huntington's Disease Society of
-        America) to present our project and discuss other ongoing research on HD such as Zinc Fingers. Most importantly,
-        we had a rare opportunity to attend an Education Day event at HDSA Center of Excellence at Columbia
-        University Medical Center and NYS Psychiatric Institute where we met Huntington's disease patients,
-        their caregivers and advocates. Through direct outreach to institutions and educational communities
-        such as our schools, the colleges/universities in our city, and affiliated organizations, we hoped to
-        inspire further experimentation and interest in HD.</p>
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