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LOVE THE LYMPHEDEMA TREATMENT ACT- VALENTINES WALK 2017

Team Member: Michelle Ferranti

Michelle's Photo
Michelle's Photo
Michelle's Photo
Michelle's Photo
Michelle's Photo
Michelle's Photo
Michelle's Photo
Michelle's Photo
Michelle's Photo
Michelle's Photo
Michelle's Photo
Michelle's Photo
 

We did it!
February 15, 2017

Thank you so much for helping me exceed both my fundraising and mileage goals!!  Together we raised $70 and I walked 3.7 miles today.  On behalf See More

EVENT DATE Feb 14, 2017

THE STORY:

Hi Friends!  I was thrilled when my sister, Heather Ferguson, invited me to be her 'plus one' for the Love the Lymphedema Treatment Act Valentines Walk 2017!!  Thank you for visiting my page!

As many of you know, I adore my twin nephews more than words can express, and I love them extra-extra-special because of how the entire Ferguson family has worked together to tackle Dylan's diagnosis of Primary Congenital Lymphedema as a team!  Lymphedema can be scary because we know there is no cure (yet!), but the passage of the Lymphedema Treatment Act (LTA) will ensure that patients receive the care they need until that day comes.  Can you imagine that Dylan's private insurance used a loophole to repeatedly deny coverage for his treatment!?!  My sister took Dylan's fight for coverage all the way to the North Carolina legislature and a state mandate was enacted ensuring coverage for lympadema patients in North Carolina.   Now, there is a national bill - The Lymphadema Treatment Act - that would help patients all over the U.S. 

I'll be walking solo in Boston (I'll be there for work), and I ask you to support my efforts in one of two ways!  The first method costs nothing but a few minutes of your time.  Please visit http://lymphedematreatmentact.org/ and send an email to congress urging them to pass the LTA!  This is cost-neutral, life-saving legislation!  If you want to show further support, you can sponsor me for a few dollars as I walk to achieve my goal of raising $50 to support the 3-5 million Americans living with Lymphedema. 

Thanks and Love,

Michelle

Lymphedema Advocacy Group Board wrote -

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 “Join the Team” 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. 

$70

 

140% Raised of $50 Goal

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  • Janessa and Ed

    $10

  • Anonymous

    $25

  • Sara

    $10

  • Jeanette and Jeff

    $25

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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

Jeanette and Jeff

Jeanette and Jeff

DONATION: $25

6 months ago

Sara

Sara

DONATION: $10

7 months ago

Anonymous

ANONYMOUS

DONATION: $25

7 months ago

Janessa and Ed

Janessa and Ed

DONATION: $10

Go Michelle! We are happy to support this cause for your family! 7 months ago

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