Amazon icon Audible icon Autographed icon Book Bub icon Booksprout icon Buy Me a Coffee icon Email icon Facebook icon Goodreads icon Instagram icon Mastodon icon Patreon icon Periscope icon Pinterest icon RSS icon Search icon Snapchat icon TikTok icon Tumblr icon Twitter icon Vine icon Youtube icon LinkedIn icon

Tag: nutrition speaker

Come See Elizabeth Yarnell in January 2014

Reader question: I found you on Amazon. Do you have any speaking or demonstrations events scheduled for 2014? None seem to be on the website calendar. ~ Susan A., Evergreen, COYarnell_red_web

Hi Susan. So nice to meet you, and thank you for noticing that I had not yet updated my online calendar to reflect my January engagements.

It has now been done and you’ll see that I have a book-signing at the Bookworm bookstore in Edwards, Colorado (outside of Vail) on January 20th (Martin Luther King Day), as well as a lecture on eating healthily in our toxic world in Denver on January 26th. Both events are open to the public and I would love to see you there!

If any of my readers would like me to come speak at an event, please feel free to contact me directly or suggest my services to the event organizer.  I love speaking to groups of all sizes and demographics as long as they are interested in how they can improve their health through better eating.

And really, who isn’t?

 

NMO is not MS

The 2012 class photo of NMO patients.

This week I was fortunate to be invited to speak at the Guthy-Jackson Foundation’s annual symposium on neuromyelitis optica (NMO). Originally known as Devic’s Disease, NMO is currently an incurable but treatable autoimmune disorder. The body’s immune system attacks its own healthy cells, most commonly in the optic nerves and spinal cord. It can cause temporary or permanent blindness and/or paralysis, and may have periods of remission and relapse.

Me with Victoria Jackson at the NMO Symposium.

Often mis-diagnosed as Multiple Sclerosis, far fewer people have been diagnosed with NMO. So few, in fact, that when Victoria Jackson and her husband Bill Guthy’s daughter was diagnosed with NMO five years ago, there was no information to be found anywhere on the internet about NMO. The Guthy-Jackson Foundation is dedicated to funding basic science research to find answers that will lead to the prevention, clinical treatment programs and a potential cure for Neuromyelitis Optica (NMO) Spectrum Disease. Each year, the foundation brings together doctors, scientists, and researchers to exchange information and knowledge about NMO. On the symposium’s final day, NMO sufferers fly in from all over the USA and from seven other countries to participate in educational sessions and be part of the NMO community.

As with any other disorder, eating healthily can only help the body have more resources with which deal with the effects of a disease process. My general advice for healthy eating is to focus on real, whole foods rather than processed foods, and to eschew chemical additives in any form. These days, my advice includes avoiding GMO foods whenever possible.

I tip my hat to these brave folks fighting this rare disease.