The Chronically Awesome© Foundation is a philanthropic organization whose mission it is to cultivate and support the Chronically Awesome Community through artistic programs including but not limited to blogging, photography, painting, and crafting; as well as to provide support programs both in a group or peer-to-peer settings. The Chronically Awesome Foundation strives to educate and raise awareness about the needs of the Chronically Awesome. We provide comfort to those in need and give back to The Chronically Awesome Community in creative and uplifting ways. Find out more.
The programs of The Chronically Awesome Foundation are based on support, acceptance, diversity and peer inspiration. We help one another set and achieve goals with our chat groups, podcast, and social communities. Click on one of the programs below for more information.
Get Inspired by The Blogs Of Our Members.
Chronically Awesome is Grateful All of us at Chronically Awesome are for your support. Happy Thanksgiving.
My Life With Chronic Pain After Being Misdiagnosed With Addiction By Patti A. I am writing this article from the perspective of being a patient who has a Chronic Pain Condition as well as having an unwarranted, Doctor imposed label of “Addiction”. What no one seems to really understand is that my Chronic Pain Condition is[…]
The Chronically Awesome Foundation was founded, in part, on the basic concept that writing heals. We believe that on the whole, art heals and that writing is one very powerful part of that. Everyone has a story to tell. We do not have to be great writers. We do not have to know how to spell[…]
Gifts I Didn’t Ask For (This blog by Ellie turned into a gift that I was not expecting. When you get to the end, her words will inspire you to look at your life as its Chronically Awesome gifts.) I meet the awesomely cool Jules Shapiro, founder and executive director of the Chronically Awesome Foundation[…]
I Just Want To Be Seen A Guest Blog by Ellie I Googled invisible illness. I know what they are. I live with them every day, but I wanted to see what the internet had to say about them. The internet offers up a basic and obvious definition – a chronic health condition with no[…]
This week the theme of Invisible Illness Week is SeeThe Invisible. Here are 30 Things You May Not Know About My Invisible Illness 1. The illnesses I live with are: Bipolar Disorder and it’s associated drawbacks, EDS and the degrading joint and tissue disorders that occur over time with the disease, PTSD, I am a nearly[…]
Thank you to United Advocacy Australia for sharing your Invisible Illness Week “30 Things” Meme with The Chronically Awesome Foundation. Read the original post here. 1.The illness‘ I live with are: Rheumatoid Arthritis, Fibromyalgia, Polymyalgia Rheumatica, General Anxiety Disorder, Agoraphobia, Social Anxiety Disorder, Migraines, Temporomandibular joint Disorder, I also have Hypertension and GERD 2.I was[…]
5 Sleep Tips To Help People With Chronic Illness Sleep Better And Ease Pain A guest post by Jennifer Scott of SpiritFinder.org 5 Tips To Help People With Chronic Illness Sleep Better And Ease Pain By Jennifer Scott of SpiritFinder.org People with chronic illness and those who experience chronic pain, which can be directly associated with[…]
A guest post by Adriel New Life Outlook Visit New Life Outlook Family Connections Having fibromyalgia can easily lead to feelings of loneliness. The pain and fatigue we experience make going out and socializing rather difficult. Even worse than that is the feeling that none of your family or friends understand your suffering. Your loved ones[…]
Big Questions From The Archives of Rebecca’s Blog. Do you remember when you were first diagnosed? The questions you had? The decisions you had to make? The way your life changed? AUGUST 31, 2011 ~ Rebecca R. Big Questions Because, Fibromyalgia Today I found myself being asked big questions by forces unseen; what was most[…]