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News
Genomic Medicine, Physician Dedication Give Family Answers About Teen’s Rare Disease
Through whole exome sequencing performed in 2020 at the Steve and Cindy Rasmussen Institute for Genomic Medicine at Nationwide Children’s, one family was finally able to put a real name to their adolescent's rare disease.
Article
Well-Baby Visits: 12 Months
Welcome to the 12-month visit! Your baby is now 1 year old. Learn what to expect at this visit.
News
Tickets for Butterfly Guild’s Production of Cinderella on Sale November 26
For its 64th annual production, Butterfly Guild of Nationwide Children’s Hospital is pleased to announce Rodgers & Hammerstein’s Cinderella will take place on March 4, 5 & 6, 2022 at the historic Palace Theatre located at 34 W. Broad St. This family-friendly, Broadway-quality production benefits the Hospice and Palliative Care Programs at Nationwide Children’s Hospital, the only programs of its kind in central Ohio.
News
Nationwide Children’s Hospital Joins New NORD Rare Disease Centers of Excellence Network, Committed to Improving Access and Care for Rare Disease Patients
Nationwide Children’s Hospital has been selected as a Rare Disease Center of Excellence by the National Organization for Rare Disorders (NORD), a nonprofit patient advocacy organization committed to the identification, treatment and cure of rare disorders through education, research and patient services
News
CareSource Donates More than $350,000 to Nationwide Children’s Hospital’s Center for Healthy Weight and Nutrition
COLUMBUS, Ohio – CareSource, a nationally recognized nonprofit health plan, announced today a $361,000 gift to Nationwide Children’s Hospital’s Center for Healthy Weight and Nutrition.
News
Early Phase Gene Therapy Study for SMARD1/CMT2S Disease Now Enrolling
Nationwide Children's Hospital has launched a new Phase I/IIa gene replacement clinical study to evaluate the safety of a gene therapy for IGHMBP2-related diseases, specifically spinal muscular atrophy with respiratory distress type 1 (SMARD1) and Charcot Marie Tooth disease type 2S (CMT2S). SMARD1 and CMT2S are rare inherited conditions that are both caused by mutations in the IGHMBP2 gene, of which more than 60 have been found to date. SMARD1 is the most severe form of these diseases and causes muscle weakness and respiratory failure in infancy.
News
Nationwide Childrens Hospital Staff and Kids Star in Fashion Show Hosted and Styled by Designer Christian Siriano
Lane Bryant, the nation's leading women's specialty size apparel brand, and Columbus-based Nationwide Children’s Hospital partnered to present an exclusive fashion show last night, aligning with the brand’s Give. Share. Love.
News
New Study Finds Exercise Treadmills Significant Cause of Hand Burns in Children
In recent years, home exercise equipment has become increasingly common, and treadmills have continued to be the largest selling exercise category by a large margin.
Article
Coping with Medicines
Children or teens may need medicine to manage their disease. Some medicines may have side effects, like unwanted changes in their mood or how they look.
Blog
Car Seat Rules Are Changing-What You Need To Know
There is nothing more overwhelming to a newly pregnant woman than walking into a baby super store. I like shopping, but I was on the verge of a full- blown panic attack when I went to register for my first child and the woman behind the counter handed me a folder of everything you