Tonight, the United Multiple Sulfatase Deficiency Foundation put on a fundraiser at the Ohr-O’Keefe Art Museum in Biloxi. The funds raised through tonight’s fundraiser will go towards research, spreading awareness and finding a cure for MSD, the rare disease that…
Tonight, the United Multiple Sulfatase Deficiency Foundation is putting on a fundraiser at the Ohr-O’Keefe Museum to raise funds for the rare, fatal, and inherited disease. News 25’s Veronica Bayona has the details.
A little girl with a rare and fatal disease needs support from the community and this week is your chance to help out. Four-year-old Willow from Ocean Springs has multiple sulfatase deficiency, or MSD, and Warriors for Willow is a…
While many people are wishing for presents this Christmas, one Ocean Springs family is praying for a miracle. That is to save a special little girl from a deadly disease that has taken a severe downturn since last year. From…
An Ocean Springs family is rallying around their little girl as she fights for her life against a rare disease. They are now calling on the community for support. A band of warriors is answering that call to help three-year-old…
News 25's Bryan Kennedy interviews Jeremy London and Jason Edwards about Monsters Anonymous movie creation and premiere this Saturday, Sept 24th Beacon Theater.
This weekend, two events will be taking place to help benefit a few Mississippi residents. If you're a runner or walker and want to give back to the community, there is an event for you this weekend. The sixth annual…
One Coast family’s three-year-old is fighting for her life and they need your help. Willow Cannan is the daughter of Amber Olsen and Tom Cannan. She suffers from a rare genetic disease affecting less than 50 children in the world.…