#JustLikeJaden

Be ‪#‎JustLikeJaden‬ and support, Life Without A Fork’s, Supervising Producer, Katya Williams’ ongoing funding campaigns to find cure for the rare, life-threatening condition, idiopathic angioedema. That’s right, we would love to have your children take part in saving lives, too! Here’s how it works:

To be #JustLikeJaden, write a short letter introducing yourself and why being an advocate for idiopathic angioedema is important. Aim your letter towards health food stores such as Whole Foods, Trader Joes, Costco’s, other natural foods markets, educational stores like Barnes & Noble, pharmacies such as CVS or health supplements stores like GNC. Pretty much anywhere a person might shop for everyday necessities would be a great place to start.

And don’t think we left you moms and dads out on all the fun. You can partake in this history-making outreach initiative by contacting your own local media outlets, radio and local news organizations to get the word out. Don’t wait–DO IT, NOW!

Ask them to support, Life Without A Fork, and help advocate for idiopathic and all forms of angioedema. The more awareness we have, the farther our message goes. If applicable, be sure to emphasis how chronic angioedema has impacted your life and health as well.

You can also donate at the link below:

https://www.gofundme.com/LifeWithoutAFork

Leading advocates, worldwide, for the rare, life-threatening condition‪#‎IdiopathicAngioedema‬–we are ‪#‎The80Percent‬!

Thanks for sharing in our page’s posts, events, and overall advocacy efforts. Please like and invite your friends to like our page.
Follow us on Instagram: @LifeWithoutAForkDocumentary
Follow us on Twitter: @LifeWithouta4k
We appreciate your ongoing support!


~ Donate Here for Filmography ~

Life Without A Fork Is A Not-for-Profit | 501(c)(3) | Corporation

As always, we appreciate your ongoing support.

Disclaimer: Our page is a community service to our users. The information provided on this site is meant for informational purposes only. LifeWithoutAFork.com, Inc., The Idiopathic Angioedema Global Advocacy Group, and its employees and affiliates are not responsible for the accuracy of any information herein contained. You are encouraged to validate any information we provide with proper professional consultation.

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.

One thought on “#JustLikeJaden

Comments are closed.

<span>%d</span> bloggers like this: