Best Team Performance Nominees

The directory does not include all nominees. Only nominees who have created a directory profile are shown. If you have been nominated for an award and have not received an email to be included in the directory please email awards@wegohealth.com

The Frey Life

We are daily vloggers on YouTube showing the ups and downs of everyday life with Cystic Fibrosis! Encouraging…

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Barby Ingle

Barby is an advocate for PTs w 150+ Chronic & Rare Diseases | Pres. International Pain Foundation (vol…

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jaimelynmoy

My story begins, not with me, but with my son, Andy. At age 4 he was diagnosed with psoriasis and a year…

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BA Andrews

The Riland Changing the Face of Lupus scholarship is available at both ClaIflin and SC State Universities…

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Young's People Chronic Illnesses

Young People, Chronic Illnesses is an Instagram page that was started in 2015. It is run by a group of…

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Boldlipsforsicklecell

I am one half of the team @boldlipsforsicklecell Jew-EL Darbone I'm 27yr old black female with sickle…

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International Autoimmune Encephalitis Society

International Autoimmune Encephalitis Society (IAES) is a Family/Patient centered non-profit that assists…

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Paul

A passionate care giver who wanted to do more to raise the profile of and give overdue recognition for…

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Jimmy

I feel i am very blessed in that i am able to give back to EVERY COPD patient who wants to learn and…

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Central Pain Nerve Center

We, Becky Brandt, RN & Lisa Davis Budzinski, started the CPNC to share comprehensive medical information…

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Sue L. Hall, MD

I am a neonatologist,; before medical school I was a master's level social worker. My passion involves…

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Sherri Holdren

I am 58 years old with stage 4 COPD I for the longest time didn't understand what's COPD was and I further…

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Brain Energy Support Team (BEST)

The Brain Energy Support Team is a 501c3 nonprofit organization founded in 2008. BEST provides peer support…

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Critical Mass: The Young Adult Cancer Alliance

Critical Mass: The Young Adult Cancer Alliance is a community-powered 501(c)3 advocacy organization that…

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Alexa Chronister

After I was diagnosed with Ehlers Danlos Syndrome & Dysautonomia in 2016, I desperately sought to derive…

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AME - Amigos Múltiplos pela Esclerose

AME was born to make people with MS have a better life. Since then, abides by the principle that #InformationIsTheBestMedicine.…

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Dysautonomia Support Network Volunteer Team

Dysautonomia Support Network is a US based 501 (c) 3 organization that provides support, resources, education…

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Jen Lee Reeves

I am the co-founder of Born Just Right, a nonprofit organization focused on giving kids with disabilities…

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Jo Grey (Association for Multiple Endocrine Neoplasia Disorders)

I've been involved with AMEND since shortly after being diagnosed with MEN2A in 2000 after narrowly surviving…

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