IAE Dreams Come True

Help make someone’s dreams come true 2017 and beyond with Life Without A Fork’s Precious Collectible Dolls! Absolutely adorable and great feel-good companions for the heart!On 18 December 2016 and just in time for the holiday season, Global Angioedema Advocate, Vanessa Williams, met with and gifted the Life Without A Fork Collectible Doll, Kelsey, to beautiful 18-year-old hereditary angioedema survivor, Victoria Inamagua, in Hollywood, California!

Per Vanessa Williams recommendation, Victoria had successfully travelled from Mineappolis, MN to San Diego, CA to see leading angioedema specialist, Dr. Marc Riedl. It was a great visit overall for Victoria and it took a lot, financially and physically, for her to make both trips, to see Dr. Riedl and to have the opportunity to meet with Vanessa Williams in Hollywood who later received this text from her mom, Nina Riechard, “It was so great to see you! And thank you so much for EVERYTHING!!!! You are officially another mom for Vikki! We will definitely be keeping in touch…”

Your support is vital in enabling us to continue our advocacy efforts! By donating $250 or more you will receive one of our beautiful antique treasures to keep for your personal enjoyment or you may also gift your doll to a charity or child of your choosing who may be living with angioedema, mast cell activation disorders, urticaria, anaphylaxis, Crohn’s and any other chronic invisible disability.

We need media attention around our outreach efforts like, yesterday! Please contact your local news media, churches, and health food chains, as well as your favorite talk show and radio show hosts, bloggers, YouTube personalities, and more, and mention the great work Vanessa Williams has been doing for so very many years as well as the importance of our cause for #AngioedemaCure. It really does take a village!

We appreciate your ongoing support!


#MayYourSwellsForeverBeMinimalatMost | #InSearchofACure | #IdiopathicAngioedema | #The80Percent |  #TheLifeWithoutAForkIdiopathicAngioedemaAdvocacyGroup |#NonProfit |#VanessaWilliams | ‪#‎ExecutiveProducer‬ |‪#‎WorldRenownedAngioedemaAdvocate‬ | ‪#‎Documentarian‬ | ‪#‎Director‬ |‪#‎KatyaWilliams‬ | ‪#‎SupervisingProducer‬ | ‪#‎ChillWill‬ | ‪#‎CoProducer‬ | #KellyHilaire ‪| SportsMedicine | #‎LifeWithoutAForkDocumentary‬ |‪#‎LifeWithoutAFork‬ | ‪#‎FilmYouProductions‬ | ‪#‎Angioedema‬ |‪#‎ChronicRecurringIdiopathicAngioedema‬ |‪ #‎BradykininMediatedAngioedema‬ | ‪#‎HereditaryAngioedema‬ | #FoodAllergies | #RareConditions | OrphansConditions| ‪#‎DrMarcRiedl‬ | ‪#‎LeadingAngioedemaSpecialist‬ |‪#‎USHAEAAngioedemaCenteratUCSD‬ |#MentalHealth | #JumpingOutOfBuildingsDocumentary

Follow us on Instagram: @LifeWithoutAFork
Follow us on Twitter: @LifeWithouta4k


“Co-creators of the universe and futurists in their unique and respective visions, Vanessa Williams and Katya Williams are, “compelled to help grow the collective’s ability to self-develop mentally, physically, emotionally and spiritually, to completely transform as human beings, and initiate what’s new in the now!”


To help keep our global outreach efforts free we ask that you donate to our ongoing https://www.gofundme.com/LifeWithoutAFork campaign below and most sincerely hope that your swells will forever be minimal at most.

“DONATE NOW AND SUPPORT LIFE WITHOUT A FORK’S ONGOING OUTREACH INITIATIVES TO CURE #IDIOPATHICANGIOEDEMA!! MAKE HISTORY WITH US AND HELP CURE IA TODAY! WE TRULY APPRECIATE YOU!” #THE80PERCENT

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

As always, we appreciate your ongoing support.

Laura | Life Without A Fork Collectible Doll

 

Source: IAE Dreams Come True

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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