This post is part of the Epilepsy Blog Relay™ which will run from March 1 to March 31, 2018. Follow along!
Emma’s blog, Little Mama Murphy, shares stories from a family living with the ‘medical mystery’, of an undiagnosed child. Stories include stressing about coming to terms with the lack of a diagnosis to videos showcasing recent successes. Emma jokes, “I’m basically using the Internet as free counselling! So far it seems to be working as I haven’t had a nervous breakdown. Yet!”
Emma Murphy’s 7 year old son Hugh has complex, drug resistant epilepsy and life threatening seizures as a result of his recently diagnosed genetic condition FOX G1 Syndrome. She blogs about their journey towards a diagnosis and their triumphs and challenges with epilepsy at Little Mama Murphy.
TWITTER CHAT: And don’t miss your chance to connect with bloggers on the #LivingWellChat on April 2 at 7PM ET.
Founder and CEO
Jessica brings a unique perspective to this leading epilepsy blog as she was diagnosed with epilepsy as a teen. She also brings 20+ years experience in marketing.