I have to be health-conscious because of my current medical issues attributed to my craniofacial disorder. However, I still love my sweets. This #vegan eggnog recipe contains raw Cashews, Dates, and Banana. It is delicious, nutritious and super easy to make! 😋 http://bit.ly/2lhXKpf
Cynthia is a Graduate Student and Craniofacial Awareness Advocate born with Treacher Collins Syndrome. She currently works as a health and wellness activist with her husband through their FREE charity app Assuaged. The Murphys are passionately seeking to bridge the gap between healthcare and self-care to meet the needs of healthy living as a method for longevity. They are going beyond charity and unifying people through love and compassion.
Friday, December 29, 2017
Forest Born With Charge Syndrome Has Spent His Entire Life in Hospitals. Now His Parents Need Help Bringing Him Home
One-year-old Forest Kanode has spent the entire first year of his life in a hospital. He had surgery at 7 days old and then he had a second heart surgery at 2 months old.
Forest’s heart problems were just part of what he’s dealt with. He was also diagnosed with CHARGE syndrome, a #craniofacial disorder that can affect a child’s eyes; heart; sinuses, esophagus and trachea; development; genitals and ears. http://bit.ly/2BRhoyG
Thursday, December 28, 2017
Craniofacial Conditions: Apply to Win a Cochlear Baha Advanced Hearing Aid Processor
Vegan Eating Set to Be 2018’s ‘Mega-Trend’ as Plant-Based Sales Triple in One Year
Plant-based #veganism is the new #health food trend of 2018! This is so exciting! :100: http://bit.ly/2BMJGdN
Casting Call for Young Girls with Disabilities
Calling all #craniofacial parents! Check out this amazing modeling opportunity provided by Changing the Face of Beauty! http://bit.ly/2zFrKzH
Wednesday, December 27, 2017
Raising Awareness for Facial Differences One Smile at a Time
Friday, December 22, 2017
The Multiple Benefits and Uses of Yarrow
Wednesday, December 20, 2017
Media News: The Love Story Behind Assuaged
The Assuaged owners Thane Murphy (Disabled USMC Veteran) and Cynthia Murphy (Treacher Collins Syndrome) have a unique 'rags-to-riches' love story that made its way across the media news!
Follow the link to watch the video by Barcroft Media! http://bit.ly/2Ba9zUC
Daily Mail Reports: Woman told she was too ugly to #love and spent her childhood being beaten and #bullied has finally accepted her severe facial deformity because to her husband she is ‘the most #beautiful woman in the world.’
Monday, December 18, 2017
Singapore Street Noodles Recipe—Nutritious Healthy Comfort Food
Looking Passed the Face to the Person Within
Jennifer Wallace reflects on her journey and the documentary she was inspired to create. Her first surgery at 22 months old and continued through more than 16 additional surgeries to correct facial damage caused by a #craniofacial #hemangioma, a benign growth of blood vessels. Story published by Wells Fargo Stories. http://bit.ly/2CvLxDx
Wednesday, December 13, 2017
A Plant-Based Lifestyle with No Judgment, No Remorse
Couple With Rare Disorder Meet, Get Engaged
A beautiful love story that begins in 2013. Erin, from Linwood, has Moebius syndrome, a rare #craniofacial disorder that causes facial paralysis. According to the United States National Library of Medicine, the condition affects 1 in 50,000 to 1 in 500,000 newborns. http://bit.ly/2z7gqzr
Tuesday, December 12, 2017
The Link Between the Rising Costs of Human Health Care and Pet Health Care
Consider a plant-based diet to help reverse disease today!
Saturday, December 9, 2017
Anthony was born with Craniosynostosis
Anthony was born with #craniosynostosis, a common #craniofacial disorder. His skull was fused together, preventing growth. But doctors noticed something amazing. http://bit.ly/2yRElms
Craniofacial Doctor Andrew Wexler Retirement Gathering
The farewell gathering for Dr. Andrew Wexler was an amazing turnout. They even pulled my patient chart and had it out on the table. It was funny but so meaningful! 💖
Many patients didn't show because of the wildfires in Los Angeles, but several of his colleagues attended, I lost count! I'm so thankful for Dr. Francis helping me to arrange the occasion.
I met some incredible people on The Kaiser West LA #craniofacial team. These are amazing people who truly care to make a difference in our lives. Without their delicate care all these years, I wouldn't be here today. I'm forever grateful.
Dr. Wexler thank you for making such a positive impact on my life! You will be deeply missed by all!
Wednesday, December 6, 2017
Dr. Francis Smith, Treacher Collins Syndrome
Francis was born with Treacher Collins Syndrome and works as a scientist. He is also an accomplished classical pianist and violinist. We've spent quality time together at every retreat. He's like the brother I never had.
Francis you are a remarkable man. I'm so grateful to have you in my life! We can't wait until our next adventure at the CCA retreat! The girls and I are already talking and planning!
http://cbsloc.al/2Au8Xf0
Monday, December 4, 2017
Cassidy and Sophie, Treacher Collins Syndrome
Cassidy and Sophie treat each other more like sisters, despite having only met recently. The two girls were born with Treacher Collins Syndrome, a rare genetic disorder that results in facial abnormalities of varying degrees. http://bit.ly/2A0Rhsa
Saturday, December 2, 2017
Chocolate Chunk Maple Glazed Pumpkin Loaf Recipe
This Chocolate Chunk Maple Glazed Pumpkin Loaf recipe is delicious and easy to make! Browse more healthy #recipes on our FREE Assuaged iOS App!
Enjoy conveniently linking within the app and discover dual-certified USDA Organic and Non-GMO Project Verified products to buy in BULK and SINGLE for CHEAP!
Find plant-based recipes for #health conditions, body essentials products, DIY #beauty, mapquest to stores and MORE! https://itunes.apple.com/us/app/assuaged/id1300506711?mt=8
Adapt to an #organic #vegan blue-zone lifestyle for #wellness and #vitality today!
Friday, December 1, 2017
Zoey Tidwell, Battles Complications from Rare Craniofacial Condition
Adorable Zoey Tidwell from Saucier in Mississippi, USA, battles many complications caused by severely undergrown facial bones, including difficulties breathing and feeding. Zoey has an ultra-rare #craniofacial syndrome. She starts her marathon surgery list to fix her face and help her to lead a normal life. http://bit.ly/2khXs4k