Skip to content

LOVE THE LYMPHEDEMA TREATMENT ACT- VALENTINES WALK 2017

Team Member: Julie Hanson

Julie's Photo
Julie's Photo
Julie's Photo
Julie's Photo
Julie's Photo
Julie's Photo
Julie's Photo
Julie's Photo
Julie's Photo
Julie's Photo
Julie's Photo
Julie's Photo

EVENT DATE Feb 14, 2017

THE STORY:

Hi. My name is Julie Hanson and I'm a board member at the Lymphedema Advocacy Group. I've been passionate about lymphedema since it became an unwelcome guest in our home five years ago when our daughter Sophia was diagnosed. As a physician and mother I'm well aware that compression is the cornerstone of treatment for people suffering with lymphedema. Our daughter is fortunate enough to have access to compression garments and supplies but I can't imagine what her life would be like without this vital treatment. So many families are not so fortunate. Please support the Lymphedema Treatment Act and the millions suffering by sponsoring my walk this Valentines Day and by writing and calling your representatives to insist on their support for our bill

I pledge to walk 5 K on Valentines! 

Won’t you support me with a donation? 

-------------

Why Are We Fundraising?

Because passage of the Lymphedema Treatment Act is critical! You can read about why here

Every two years, The Lymphedema Treatment Act (like all other bills awaiting passage) enters a new Congress and must begin again to renew and broaden its Congressional cosponsorhships. A big part of that process involves around one hundred volunteers from across the country traveling directly to Washington for an event known as "Lymphedema Lobby Days". You can read more about Lobby Days here. Lobby Days has traditionally garnered dozens of critical cosponsors for the LTA, however, the event is not without expense. This is where you come in! 

How can you help? There are two options to chose From: 

1) Donate: Just click the "DONATE" button to make a secure online donation. 

Note: If you’d feel more comfortable donating by check, you can make checks payable to The Lymphedema Advocacy Group and mail them to: The Lymphedema Advocacy Group, PO Box 1682, Carrboro, NC 27510.

OR...

2) Join “The Team”: If you are feeling even just a little adventurous, you could click the “Fundraise for This Campaign” button and walk in your hometown. When you join, you can "edit" your walk page to personalize it like Sophia's below. You can watch a brief "how to" video we've prepared by here. 

You can then easily share the fundraiser links via social media (such as Facebook, Twitter, or email) with friends and family. Let them know that you have joined the walk and ask if they might support you and your cause with a donation. We just ask that you spread the word, walk on February 14th, and donate! 

As far as the walk, you can walk 10 feet or 10 miles! You can walk on your own or bring friends! You can walk indoors or out! Whatever you like and whatever works for you!

Other great stuff:

  • You can download a flyer to print and handout or a flyer for use as an email attachment by clicking here
  • If you’d like some LTA swag (like t-shirts and bags) you can pick them up by here!   
  • Send us a pic of you on the walk and we’ll upload it to our Facebook page! 

IMPORTANT: Our walk waiver can be found here and by signing up to join the team you are acknowledging that you have read and understood the waiver. 

Note: Contributions or gifts to the Lymphedema Advocacy Group are not tax deductible. As a 501(c)(4) nonprofit organization, the Lymphedema Advocacy Group engages in lobbying activity, in keeping with its mission, for passage of the Lymphedema Treatment Act. 

$550

 

110% Raised of $500 Goal

  •  
  •  
  •  
  •  
  •  
  •  
  •  
  •  
  •  
  • Wayne & Sharon Fesler

     

  • Charlene Behrends

     

  • Renee & Gregory Cole

     

  • Julie & Randy Olberding

     

  • Doug Olk

     

  • Anonymous

     

  • Beth Bonner

     

  • Best Sister Ever

     

  • Greg and Peggy Miller

     

  •  
  •  
  •  
Organized by

Lymphedema Advocacy Group Board

This is a direct to organizer fundraiser.

Fundraise for this Campaign

The Team: $23,486 TOTAL RAISED SO FAR

JOIN THE TEAM
Fundraiser Title

Elaine Eigeman

Amount Raised

$7,834

 

392% Raised of $2,000 Goal

Fundraiser Title

Lymphedema Advocacy Group Board

Amount Raised

$5,828

 

29% Raised of $20,000 Goal

Fundraiser Title

Becky Sharp

Amount Raised

$1,600

 

320% Raised of $500 Goal

Fundraiser Title

Bill McCann

Amount Raised

$1,196

 

239% Raised of $500 Goal

Fundraiser Title

Sophia Hanson

Amount Raised

$1,180

 

118% Raised of $1,000 Goal

Fundraiser Title

Barbara Coyle

Amount Raised

$825

 

165% Raised of $500 Goal

Fundraiser Title

Cindy Cronick

Amount Raised

$728

 

146% Raised of $500 Goal

Fundraiser Title

Jill Ryan

Amount Raised

$650

 

43% Raised of $1,500 Goal

Donor Comments

Greg and Peggy Miller

Greg and Peggy Miller

Compression hugs :) 8 months ago

Best Sister Ever

Best Sister Ever

9 months ago

Beth Bonner

Beth Bonner

9 months ago

Anonymous

ANONYMOUS

9 months ago

Doug Olk

Doug Olk

9 months ago

Julie & Randy Olberding

Julie & Randy Olberding

For you! 9 months ago

Renee & Gregory Cole

Renee & Gregory Cole

9 months ago

Charlene Behrends

Charlene Behrends

9 months ago

Wayne & Sharon Fesler

Wayne & Sharon Fesler

9 months ago

Report this page — Let Us Know if you think this page is breaking the law or the CrowdRise Terms