Caden and his family’s journey with Children’s Miracle Network and Dance Marathon began when Caden was just four weeks old. At four weeks, Caden was diagnosed with Hemophilia A, which means that if Caden fell or got a cut, unlike our bodies, Caden’s body isn’t able to produce a fibrin clot and stop the bleeding. November 2017 brought a lot of changes for the Buth family, as Caden stopped taking his immune suppression drugs and a new weekly subcutaneous Hemophilia therapy was approved by the FDA. Caden’s family is happy and ecstatic to report Caden hasn’t experienced a single bleed and his quality of life has increased by leaps and bounds. No more missed school or play dates, no more worrying if he falls or plays outside too much. Although Caden’s treatment is still regulated by various specialists at Shands, many of the complications Caden and his family once endured has been alleviated as a result of the funds raised by DM at FSU.