Life Without A Fork

IAE News

About

Life Without A Fork was founded by Vanessa Williams in 2009 initially as a documentary film project to bring awareness to the rare, potentially fatal condition from which she was diagnosed in 2006, idiopathic angioedema. Since then, her efforts have grown to her becoming, inarguably, the world’s leading advocate for Recurring Idiopathic Angioedema (RIA) and creating the Idiopathic Angioedema Global Advocacy GroupExecutive Producer of the feature length film which started this movement, Life Without A Fork also does ongoing research and outreach for Bradykinin Mediated Angioedema (BMA)Mast Cell Activation Disorders (MCAD)idiopathic anaphylaxis (IA)urticaria(hives), mental health diseases–“Dis-ease of the mind causes disease in the body,” her mom, Katie Tucker often told her–as well as other, seemingly overlapping conditions.

We hope you get the answers to your many questions about idiopathic angioedema–particularly those of which, ‘you do not know, you do not know’ as they are often the toughest to ask, yes? and gain the support of a global community of fellow-sufferers who understands the many extremities of your ongoing, ever challenging, and far too frequently changing circumstances.

May our outreach efforts, Idiopathic Angioedema Global Advocacy Group, feature length film, Life Without A Fork, documentary, {see trailer with the film’s starsVanessa Williams and Leading Angioedema SpecialistDr. Marc Riedlof US HAEA Angioedema Center–UCSD}, and abundance of many other resources–yes, we’ve been doing this long time, help be your roadmaps in finding guidance as to why, how, and where to seek the best and most current in qualitative medical treatments the world over as well as help find the reassurances you may need in knowing that, although absolutely, ofttimes relentlessly, bizzaro and potentially fatal, with proper care, these conditions can be manageable and usually survivable.


Help get the word out! We need A-list celebrities and media attention around this cause and like, yesterday–Oprah, come find us! Tell everyone you know what, Life Without A Fork is doing to raise awareness around angioedema and save lives! Tell us who and what you know! Donate whatever you can! Let us know how you feel you may best assist!


The Life Without A Fork Team:

Top to bottom/left to right:

| Vanessa Williams | Founder and CEO | Leading Angioedema Global Advocate | Producer | Master of Arts | Educational Theory & Practice | Secondary English

| Katya Williams | President | Director |Producer | Actress | Professional Music Entertainer | The Russian Katya

| Chill Will | Director | Professional Music Entertainer | The Get Fresh Crew | Producer

| Kelly Hilaire | Director | Sports Marketing & Management | Producer

| Marcus Anderson | Director | Fine Arts Artist | Humanities

 


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

Life Without A Fork Is A Not-for-Profit Corporation

“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

           

Source: About

Membership

To become a member of The Life Without A Fork – Idiopathic Angioedema Global Advocacy Group and get exclusive access to “member only” content on our site, follow the link below and complete steps for registration.

Benefits to Being A Member:

  • Reduced rates for 2017 Annual #SwellnessExpo!
  • No fees for articles published in Life Without A Fork
  • Discounts for purchases for, “Life Without A Fork,” documentary.
  • Access to the members-only Web Porta
  • Free subscription to Life Without A Fork publications
  • Policy resources and representation in advocacy efforts
  • Access to the Life Without A Fork Trainee Forum on various social media sites.
  • Leadership opportunities: members may be elected to serve as formal ambassadors for and represent Life Without A Fork in community activities.

Click Here And Join Us Today!

#TheLifeWithoutAForkIdiopathicAngioedemaAdvocacyGroup | #MayYourSwellsForeverBeMinimalatMost | #VanessaWilliams | #KatyaWilliams | #ChillWill | #KellyHilaire

Source: Membership

IAE Dream Dolls

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, Global Angioedema Advocate, Vanessa Williams, met with and gifted the Life Without A Fork Collectible Doll, Kelsey, to beautiful 18-year-old #hereditaryangioedema #survivor, Victoria Inamagua, in #Hollywood, California!

Per #VanessaWilliams recommendation, Victoria had successfully travelled from Mineappolis, MN to San Diego, CA to see leading angioedema specialist, #DrMarcRiedl. 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…”

12.18.16 | Beautiful Kelsey, a Life Without A Fork Collectible Doll has lovingly been gifted to hereditary angioedema survivor, Victoria Inamagua! | Happy holidays, Vikki, from Vanessa Williams and The Life Without A Fork Advocacy Group!

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, Chrohn’s and any other chronic invisible disability.

 


#TheLifeWithoutAForkIdiopathicAngioedemaAdvocacyGroup | #MayYourSwellsForeverBeMinimalatMost |                                                   #VanessaWilliams | #KatyaWilliams | #ChillWill | #KellyHilaire

Narubi

Source: IAE Dream Dolls

Documentary

IAE Dream Dolls

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, 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 pysicall, 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, Chrohn’s and any other chronic invisible disability.

#TheLifeWithoutAForkIdiopathicAngioedemaAdvocacyGroup | #MayYourSwellsForeverBeMinimalatMost | #VanessaWilliams | #KatyaWilliams | #ChillWill | #KellyHilaire

 

Laura | Life Without A Fork Collectible Doll

Source: IAE Dream Dolls

Love Gifts | Vanessa And Katya <3

Join in the celebration and appreciation of, Life Without A Fork‘s, Founder, Executive Producer and Director, Vanessa Williams, along with the company’s President, Her Heart, daughter, best friend (these two go everywhere together!) and Supervising Producer, Katya Williams!

They’ve got a “well-deserved to be spoiled,” wish list (these two women have given daily, tirelessly, without fail and without pay for over seven years) and are registered at the links below. Feel free to join The Life Without A Fork Advocacy Group, The Idiopathic Angioedema Advocacy Group, Cali Girl Entertainment, #MuseLLC and Film You! Productions in celebrating these wonderful women in recognition of their most compassionate advocacy, and filmmaking efforts!

Also, we are working with a local promoter now to try to do something big for them in Hollywood so stay tuned for the details and thanks everyone, as always, for the support!

 

Source: Love Gifts | Vanessa And Katya ❤

#TheSwellLife

Join our advocacy group’s efforts and become a Life Without A Fork #IA Ambassador today if you too are living #TheSwellLife! 😉
EXCLUSIVE OPPORTUNITY

Receive personal consultations with Life Without A Fork’s Founder and Leading Global Advocate for #IA, Vanessa Williams!

Prices and links below. Visit our contact page now and send a request for your preferred consult!

Phone consultation | 30 minutes | $145.00

Phone consultation | 60 minutes | $245.00

Webchat consultation | 30 minutes | 245.00

Webchat consultation | 60 minutes | $375.00

#TheLifeWithoutAForkIdiopathicAngioedemaAdvocacyGroup | #MayYourSwellsForeverBeMinimalatMost | #VanessaWilliams | #KatyaWilliams | #ChillWill | #KellyHilaire

Source: #TheSwellLife

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