Doing #WhateverItTakes to Treat Rare Diseases
Doing #WhateverItTakes to fight Childhood Cancer & Sickle Cell Disease
Doing #WhateverItTakes for Anthony
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When Madisen was almost 2 years old, she told her mother she had a “boo-boo.” Little did her mother know, the “boo-boo” was actually a tumor the size of a grapefruit—engulfing her kidney.
#ChildhoodCancerAwarenessMonth #ChildhoodCancer #CCAM #WhateverItTakes
“Research is crucial to understanding rare disease,” says rare-disease expert Gyula Acsadi, MD, PhD, division head of Connecticut Children’s Division of Neurology. “When you understand the disease, you then have the knowledge to design treatments for the disease.” Dr. Acsadi joins our blog to share how Connecticut Children’s is treating and researching rare neurological disorders: bit.ly/DrAcsadiQA
#SpinalMuscularAtrophy #CharcotMarieTooth #MuscularDystrophy #DuchenneMuscularDystrophy #RareDisease
When Madisen was almost 2 years old, she told her mother she had a “boo-boo.” Little did her mother know, the “boo-boo” was actually a tumor the size of a grapefruit—engulfing her kidney. https://t.co/IdY3dgETJM
#ChildhoodCancerAwarenessMonth #CCAM #WhateverItTakes
Thank you for joining us for Connecticut Children’s Adolescent #BariatricSurgery Program’s takeover of Twitter. For questions or more information please see https://t.co/SxtEQRvNiQ or email us at obesity@connecticutchildrens.org #CTChildrensBariatrics
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