Membership

B3come A Life Without A Fork Member Today! |

Life Without A Fork’s Advocacy for Idiopathic Angioedema, “#The80Percent,” Is Making History in A Big, Big Way! Join Our Movement And B3come A Member Today! |

 

With 2021 coming in, and our incomparable world’s future weirdly and, somehow unsurprisingly already looking gazillions of light-years ahead in exploratory and oft times beyond conceivable medical breakthroughs with space-medicine, we are super excited about our company’s visionaries’ abilities to be in the now with medicine, technology and media while still maintaining the bedside manner many of our fans, supporters and #SwellCommunity have come to know, appreciate and love! We are doing big things, going to far reaching places in health, advocacy and we want to offer many new great opportunities with you!

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To b3come 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! We are excited to have each and everyone of you as part of our important movement to raise awareness for survivors and fatalities of people and families with idiopathic angioedema, and all forms of angioedema, anaphylaxis, urticaria and mast cell activation disorders!

 

 

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B3come A Life Without A Fork Member Today! |

Benefits to Being A Member:

  • Reduced rates for 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 Portal

  • Free subscription to the ever evolving, Activated Manuals for Successfully Treating And Living With Idiopathic Angioedema And Mast Cell Activation Syndromes

  • Free subscription to the ever evolving, Life Without A Fork’s IAE Guide to Living An Immortal Life

  • *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.

Please indicate your area(s) of interest:

  • Joining a support group in my area
  • Leading a support group in my area
  • Idiopathic angioedema
  • Hereditary angioedema
  • Bradykinin mediated angioedema
  • Urticaria
  • Anaphylaxis
  • Mast Cell Activation Syndrome, adult (all forms)
  • Mast Cell Activation Syndrome, children (all forms)

*LWAF does not share member names or contact information with outside agencies, companies or anyone else without your express permission.

 

Please allow 2-4 weeks for processing on all membership payments. Thank you so much.


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To help keep our global outreach efforts free we ask that you donate to our ongoing funding campaigns 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 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. Life Without A Fork, 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.