New Comic Book Penned by Teens Urges Kids with Tourette Syndrome to View the Disorder as a Strength
source: pixabay.com

New Comic Book Penned by Teens Urges Kids with Tourette Syndrome to View the Disorder as a Strength

By Caitlin Seida from In The Cloud Copy If you asked Sarah Baldwin, age 19 and a sophomore at Syracuse University, about the success of the comic book she helped…

Continue Reading New Comic Book Penned by Teens Urges Kids with Tourette Syndrome to View the Disorder as a Strength
Scientists Find That Rubella and Certain Cancers Have the Same Mutation Mechanisms
source: pixabay.com

Scientists Find That Rubella and Certain Cancers Have the Same Mutation Mechanisms

By Danielle Bradshaw from In The Cloud Copy Scientific teams at the Centers for Disease Control (CDC), the National Institute of Environmental Health Sciences (NIEHS), and other research centers have…

Continue Reading Scientists Find That Rubella and Certain Cancers Have the Same Mutation Mechanisms
Service Dogs Can Make a Difference in the Lives of Those with Addison’s Disease
source: pixabay.com

Service Dogs Can Make a Difference in the Lives of Those with Addison’s Disease

By Caitlin Seida from In The Cloud Copy Medical alert dogs can give their companions a newfound sense of independence and freedom. Enter Bill, a golden retriever owned by Laura…

Continue Reading Service Dogs Can Make a Difference in the Lives of Those with Addison’s Disease

Press Release: Rare Disease Community Calls on Congress & FDA to Enact Life-Saving Public Policy Solutions

Contact: Britta Vander Linden [email protected] 917.604.6518 30 million Americans need more treatment and diagnostic opportunities https://everylifefoundation.org/rare-disease-community-calls-on-congress-fda-to-enact-life-saving-public-policy-solutions/ (Washington, D.C., December 4, 2019) Hundreds of rare disease advocates from around the country were brought to Washington,…

Continue Reading Press Release: Rare Disease Community Calls on Congress & FDA to Enact Life-Saving Public Policy Solutions
“We Don’t Know Anything:” a Mitochondrial Encephalomyopathy Story From the Czech Republic
source: pixabay.com

“We Don’t Know Anything:” a Mitochondrial Encephalomyopathy Story From the Czech Republic

When Lucinka was born, it seemed like everything was all right. But it wasn’t. Lucinka wasn’t doing well, and a whirlwind of examinations began. First, a diagnosis couldn’t be made.…

Continue Reading “We Don’t Know Anything:” a Mitochondrial Encephalomyopathy Story From the Czech Republic