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Epilepsy Blog Relay: Emma shares the family’s VNS story

March 10

This post is part of the Epilepsy Blog Relay™ which will run from March 1 to March 31, 2018. Follow along!

Emma’s Story

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.

Check out Emma’s Post





NEXT UP: Be sure to check out the next post by Naomi at https://www.ethansstars.com/. For the full schedule of bloggers visit livingwellwithepilepsy.com.

TWITTER CHAT: And don’t miss your chance to connect with bloggers on the #LivingWellChat on April 2 at 7PM ET.

Follow Jessica K. Smith:


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.

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