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Susannah Fox

I help people navigate health and technology.

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A thank you note to Jordan Grumet, MD

April 10, 2015 By Susannah Fox 1 Comment

I Am Your Doctor, by Jordan Grumet, MD

Dear Jordan, You begin your book with a beautiful description of your public writing as a love letter to your patients and to your father, who died suddenly when you were seven years old. My heart opened at that moment and I saw you in a new light. I’ve read your blog and followed your story […]

Filed Under: key people, net-friendly docs

What I’ve been working on

April 9, 2015 By Susannah Fox 1 Comment

It’s been a busy few weeks and I’d love to share a few items in one post: I served as the emcee at the Robert Wood Johnson Foundation‘s Data for Health report release event. I attempted to capture the spirit of the event in this Storify. Here’s a post I wrote about the Data for Health initiative: Imagining […]

Filed Under: e-patient stories, key people Tagged With: cystic fibrosis, Erin Moore, Robert Wood Johnson Foundation, Smart Patients

Cystic Fibrosis For One Day

March 29, 2015 By Susannah Fox Leave a Comment

Boy wearing nebulizer mask and his mom

I shadowed a mom and her 5-year-old with CF from afar for 24 hours. It taught me more than I could have imagined about living with a life-shortening disease — and about myself. This “empathy exercise” was organized by Smart Patients, an online community where patients and caregivers learn from each other.

Filed Under: e-patient stories, key people Tagged With: cystic fibrosis, empathy, Smart Patients

Disconnectedness kills, connectedness heals

March 23, 2015 By Susannah Fox 4 Comments

If you crave inspiration, tune in to the Robert Wood Johnson’s Pioneering Ideas podcast by subscribing to the iTunes feed or listening on Soundcloud: https://soundcloud.com/rwjf-podcasts/final-cut-episode-8/s-q4foj

Filed Under: key people, research issues, trends & principles Tagged With: #RWJFpodcast, Robert Wood Johnson Foundation

Speak up: The network is our superpower

March 13, 2015 By Susannah Fox 5 Comments

I have a new post up on Medium, illustrated with this gem from a 2012 post: An excerpt: We can’t let misinformation—or worse—go by without comment. I think it’s time for more people to speak up in health care. More pediatricians should express their measles outrage. More people should chronicle the reality of living with chronic conditions.

Filed Under: ethics, research issues, trends & principles, understanding statistics Tagged With: Pew Research Center, Stanford Medicine X

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Recent Comments

  • Carrie Kimmell on Case study: Trevor’s disease: “Hi Jill – currently Brandon is walking without a limp (he is almost 15 now). He was going to undergo…” Jun 5, 14:07
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