This week, we kick off Rare Disease month, by connecting with Marissa Bishop whose son Gregory has CDKL5 Deficiency Disorder (CDD). Her passion for creating awareness for the disease was infectious. As Gregory&#39;s mom and #1 cheerleader, Marissa&#39;s a powerhouse advocate for rare disease support.
 
#CDKL5

S1:E5 Ali Lofton (parent)

An exploration of the profound journey of loss, from the enduring power of love, to the unexpected moments of laughter, and everything in between. Join us for candid conversations, led by a child-loss mom and the incredible community that has supported her since day one. We’ll delve deep into the unique perspective and heartfelt advice of caregivers, friends, family, and the child-loss community. Together, we unlock the raw and complex experience of loss through the shared stories of resilience, love, and the healing strength that emerges.