#MakeWellMondays

Hey everybody, it’s #MakeWellMondays and today we’d like to, once again, dedicate our #LifeWithoutAFork #FaceBookPage to a #survivor to champion most all survivors, the beautiful, #AllieBarnett!
 
About a week ago, leading angioedema advocate, #VanessaWilliams, had the pleasure of speaking with Allie on the phone. After a very lovingly and sisterly two-hour conversation between #fellowswellers, Vanessa was able to get a better picture on just how much in crisis our #mastocytocis and #idiopathicangioedema friend is and we welcome you to join in with sending continued love and light Allie’s way today and everyday! It really does take a village and we know that if we can get #thecollective to send positive thoughts, prayers and desires for healing, Allie stands a much better chance in finding some true value-added in her health and overall life and we thank you, beyond measure, for your care!
 
And, of course, we certainly want to know how you all are doing, now, in real time! Let us know you are still here and what’s great or even not so great in your respective worlds!
 
We love you and, knowing that each and everyone one of you are golden links to the chain of our past, current and future good and successes, we ask that you continue to spread the word about the amazing work we are doing here at Life Without A Fork!!! Wishes to all for the healthiest in mind, body, spirit, life, prosperity and love!
 
#RollCall | #TheLifeWithoutAForkIdiopathicAngioedemaAdvocacyGroup | #MayYourSwellsForeverBeMinimalatMost | #VanessaWilliams | #KatyaWilliams | #ChillWill | #KellyHilaire
THE LWAF GOLDEN CERTIFICATE FOR ONGOING #IAE HEALTH AND HEALING IS PRESENTED TO…

Source: #MakeWellMondays

Published by lifewithoutafork

In 2006, I was diagnosed with the rare and potentially fatal condition known as Idiopathic Angioedema, a histamine mediated condition that causes swelling and similar symptoms that can be brought on by little to no reason. Angioedema’s Idiopathic form is different from other forms of Angioedema in that it is not known to be of a hereditary accumulated and any specific genetic tie-ins and causes are generally unknown. A few years following my initial diagnoses I began to put intentional efforts towards advocating for cause and cure for both myself and all others that have been diagnosed with this detrimental condition. For the last eight years I have personally and with very little help, funded our advocacy efforts–in every spectrum, grown and withheld an international community base, spoken at health expos, in local schools and more about this condition, as well as written, filmed, edited, and produced a documentary film known as Life Without A Fork, telling the story of Angioedema. I have even lost my sister and many others from the condition and very recently discovered that, in addition to my nephew who was diagnosed before me, I have a brother, two sisters and an aunt who have all experienced both acute and chronic cases of idiopathic angioedema. In 2014 I coined the phrase, #The80Percent as a means of distinguishing our number and the need for right attention for the largest group of people living with this rare condition, the idiopathics! Our efforts to raise awareness round Idiopathic Angioedema and save lives, are in need of assistance! Supporting this entire advocacy all on my own is no longer an option as I am now disabled. With our 501(c)(3) non- profit organization being newly established, I appreciate any relating assistance that you may be able to provide, even sharing our efforts with your friends and family. Having started in 2009, advocating for this cause and producing a feature film has been a journey and then some! I am ill with the condition, #IdiopathicAngioedema, so it remains extremely challenging for me to forge on with taking this project to the finish line. I have been offered help, countless times and sometimes, it really gets me down when the follow-through doesn’t actually come. Oft times, it gets me to the point that I just want to say, with all the pleasantries I can muster, “no, thank you.” Doors opening and closing as quickly as the turn-style types to be found in mid-town Manhattan’s office buildings, I continue to persevere as I have finally completed, Life Without A Fork, documentary film! This project, while certain to impact audiences around the globe with its rich, vivid, and most certainly, shocking images, along with its bigger than life storylines, will also serve as advocacy to help save lives, yes, mine included, thank you very much! :), by getting some, ‘right attention,’ around #ChronicAngioedema. Absolutely a project that is near and dear to my heart, I work hard to find cause and cure for this potentially life-threatening disease. For my reward, God has not only been steadfast in his willingness to help me make this happen, he continues to remind me that, as per the great words shared by my mom, the late, Katie Tucker, “Every man is a golden link in the chain of my good.” And, although I may be flying without a net, it is through the endless source of support I receive from others, like you who are His angels and are amongst my family, friends, fellow-sufferers, fans, celebrity associates, and overall well-wishers, I fly forever on God’s wings.

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