Introducing the Official “The Spoon Theory/ I am a Spoonie” Video by Christine Miserandino

Introducing the Official “The Spoon Theory/ I am a Spoonie” Video by Christine Miserandino

A slide show movie of my life, how "the spoon theory" started, and how this HUGE internet community has been formed around the world to give support, encouragement and information by using and #spoonie to connect. This has been an incredible ride! THANK YOU! PLEASE share th

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Facebook, Twitter, and MySpace Oh My! on the web!

Facebook, Twitter, and MySpace Oh My! on the web!

We love being connected with our readers! Since we have added those "handy dandy" features at the bottom of every article, we have noticed our readers have shared our articles, posted them on their personal profiles and more. We can not thank you enough for sharing this site with your friends and fa

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Television: Keeping Kids Healthy: Lupus A Medical Mystery – Featuring Christine Miserandino

May is Lupus Awareness Month! How Will You Spread Awareness? See Christine's television appearance focusing on living life with lupus.. Keeping Kids Healthy (PBS and American Public Television) Nationally Syndicated Won a 2005 New York Emmy Award EPISODE 401 - Lupus: A Medical Mystery *Check your l

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New Slogans, New Gifts and More at the store!

May is Lupus Awareness Month! How Will You Spread Awareness? Contemplating what you should give a loved-one or close friend, suffering from a chronic illness for a get well gift?How about a Tee-shirt that reads ‘Lupus Sucks’ or ‘Fibromyalgia Sucks' ? Or "Bad Flare Day!".  Look n

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About The Author

About The Author

Christine Miserandino is a writer, blogger, speaker and patient advocate from NY. She is someone living life with Lupus. Her award winning writing has been featured in numerous newspapers, magazines, medical newsletters and television media. From the age of fifteen, Christine Miserandino has been

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Protected: A Husband’s Perspective – Lupus Advocacy Day – Washington, DC

I am proud of my wife, Christine. I am proud of the work she does for the Lupus Alliance, this website, and for our family. I am proud of her passion to help others, and the impact she has had on so many people through her speaking engagements, and of course, through I had

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Christine is being honored at the Lupus Alliance Lupus Gala Brunch

Save the Date! I am extremely proud to announce that my family and I will be honored at this year's Lupus Gala Brunch! We are so excited and hope to see everyone there. The Lupus Alliance is a wonderful organization that is very close to our hearts. We try and support the Lupus Alliance as much as p

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Christine has been interviewed for today’s “empowered patient” column.

Empowered Patient, a regular feature from CNN Medical News correspondent Elizabeth Cohen, helps put you in the driver's seat when it comes to health care. This week's topic asks the question, "Are you an obnoxious patient?". Christine was quoted in tips # 3, 4 and 5! Ms. Cohen was easy to speak with

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We are always working hard to make our website the best it can be. Now we are better then before! You have been asking for some of these new features, and we have been listening! We are very proud to announce new upgrades and site features! If you have not been to our website lately - please come to

[ 4 comments ] | [ read more ] Disclosure Policy

This policy is valid from 28 November 2007 This blog is a personal blog written and edited by me. I do have guest writers, but all submissions are approved and edited by me. For questions about this blog, please contact christine at butyoudontlooksick dot com. This blog does accept cash advertisi

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