Life Without A Fork

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IAE Dreams Come True

 

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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.

 

 

 

 

 

 


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Melissa Jane | Life Without A Fork Collectible Doll

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Laura | Life Without A Fork Collectible Doll

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Narubi | Life Without A Fork Collectible Doll


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Emily | Life Without A Fork Collectible Doll


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Dennis | Life Without A Fork Collectible Doll


T’IS THE SEASON FOR GRATITUDE, GIVING, FORGIVING, COMPASSION, GREAT HEALTH AND PROSPERITY!

PLEASE SHARE YOUR RESOURCES WITH OUR COMMUNITY. WE NEED YOUR HELP TO HELP MAKE A DIFFERENCE IN THE LIVES OF SO MANY OTHERS. 


 

We are grateful because we know that the recognition, that firm tap on the shoulder for universal support is finally here for us! For you! We’re excited because we know you all continue to play such an enriching and unique part in making great things happen in the #Angioedema, #urticaria, and #MastCellActivationDisorders worlds!

Our goals:
~To secure a minimal of ten major TV news and talk show appearances for leading #IdiopathicAngioedema advocate, #VanessaWilliams–will you do your part in making this happen?!
~Corporate Social Responsibility
~ Continue to share #LifeWithoutAForkDocumentary!

Over the years and like the foundation of the Brooklyn Bridge (an awesome study which she helped an architectural intern complete once upon a job-time) Vanessa has, unremittingly and firmly, laid the groundwork for our beyond important advocacy efforts. Alas, like her Master’s degree, it can not be rescinded! It is can not be undone. We are here!

In fact, there are many amongst this chronically ill group who are all kinds of, “degree’d-up,” and are now amongst the disabled. One of #LifeWithoutAFork‘s newest friends, Jennifer Harrison, holds a PhD and yet spends most of her time dealing with idiopathic anaphylaxis, sometimes 2-3 episodes per day. Her speech is impaired, this bothers her, immensely, she has trouble typing, and she wants so much to do more for our community of sufferers.

Like the outreach work itself, time is of the essence so hoping like Jennifer, you all will continue to survive your illness, help how and where you can, as well as check-in today and let us know you are still here how you are doing.

Katya Williams

Thanks for sharing in our gallery’s posts, events, and overall advocacy efforts.

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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.


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.

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