Posts by author:

Heather

Using Social Media to Boost Support for the LTA

September 16, 2019

  Are you on social media?   We have accounts on Facebook, Twitter, and Instagram where we share these newsletters and more. You can help us amplify our reach by liking and sharing our messages.   Last week, our newsletter listed every member of Congress not yet cosponsoring the LTA, along with phone numbers and […]

Read the full article →

Congress is back in session – these are the members who still haven’t cosponsored!

September 9, 2019

Congress returns from their long summer recess today. The members listed below have not cosponsored the LTA yet, so let’s get their phones ringing this week! Phone numbers and a call script are below. Be polite but persistent – the squeaky wheel gets the grease. Thank you for your advocacy! Heather Ferguson Founder & Executive […]

Read the full article →

Do you plan to be in or near Washington, DC this fall?

September 1, 2019

  Do you have personal or business plans to be in or near Washington, DC this fall? Or do you live nearby? If so, why not meet with your members of Congress about the Lymphedema Treatment Act while you are there! We can schedule your meeting(s), provide you with materials to bring, and coach you […]

Read the full article →

Join your Lymphedema Advocacy State Team today – it’s FREE!

August 24, 2019

Are you frustrated because one or more of your members of Congress hasn’t cosponored the LTA yet? (see list below) If so, I hope you will consider joining your state’s advocacy team if you have not already done so! As a team member you will receive additional materials and guidance to contact your members of […]

Read the full article →

Share Your Lymphedema Story to Make a Difference!

August 18, 2019

  Over the last few years we have collected over 600 patient and caregiver stories through our My Lymphedema Story campaign, but we still need more! Please consider submitting your story if you haven’t already done so. These stories are shared with members of Congress and their staff. They play a vital role in helping […]

Read the full article →

Educational and Awareness Materials Available

August 10, 2019

  All of our educational and awareness materials are available for order or free download on our website.   These materials are perfect for sharing with doctors, therapists, support groups, garment fitters and suppliers, friends, family and colleagues. Due to overwhelming demand, we are no longer able to provide the information cards completely free of […]

Read the full article →

Attend a Town Hall or District Meeting in Support of the LTA!

August 3, 2019

  Both the House and Senate are now in recess until after Labor Day. During this time, Town Halls and District Meetings are great opportunities to speak to your members of Congress directly! All of the members listed below have NOT cosponored the LTA yet. DISTRICT MEETINGS: everything you need to schedule, prepare for, and […]

Read the full article →

The 38 SENATORS who HAVE NOT COSPONSORED

July 30, 2019

  This is the last week the Senate is in session until after Labor Day. If one or both of your Senators are among the 38 who are not yet cosponsoring the LTA please contact their offices this week!   ACTION STEPS: 1.) Call his or her office using the phone number and call script […]

Read the full article →

Important Progress Update

July 27, 2019

  On Wednesday of this week the Senate Finance Committee put forth the Prescription Drug Pricing Act of 2019. The Lymphedema Treatment Act was one of a number of other provisions then added as amendments! On Thursday, some of the amendments, particularly those not related to drug pricing, were withdrawn by the sponsors of those […]

Read the full article →

Our House bill tops 300 Cosponsors!!!

July 22, 2019

Our House bill now has 302 cosponsors! Check the list below to see if your Representative is a cosponsor. If he or she is not, please use the phone number and call script provided to contact his or her office this week. This is the final week the House is in session before the long […]

Read the full article →

The 60 House Members who Cosponsored Last Year but Haven’t Yet This Year

July 15, 2019

Is your Representative on the list below? If so, he or she is among the 60 House members who cosponsored the LTA in the last Congress but have not signed back on yet this session. Please take a moment to call his or her office using the phone number and script provided below my signature. […]

Read the full article →

The 39 SENATORS who HAVE NOT COSPONSORED

July 8, 2019

  If one or both of your Senators are among the 39 who are not yet cosponsoring the LTA please contact their offices this week! ACTION STEPS: 1.) Call his or her office using the phone number and call script here – this has the most impact! 2.) Send an email using this form 3.) […]

Read the full article →

We all know someone who is at risk for Lymphedema

July 1, 2019

  Although primary lymphedema like my son was born with is rare, secondary lymphedema, particularly consequent to cancer treatment, is not. Cancer survivors have a lifetime risk of developing lymphedema. In honor of July’s Sarcoma Awareness Month, we are proud to share our board member Bill McCann’s survivorship story. Sarcoma has a 30% lymphedema incidence […]

Read the full article →

Members of Congress are home again next week!

June 27, 2019

  Next week is a recess week for Congress, meaning that members will be home in their states and districts. Some will be attending July 4th celebrations and others will be holding Town Hall meetings.   Here are three ways you can find out about these events, which are often announced with very little notice: […]

Read the full article →

Welcome to the Lymphedema Treatment Act Blog!

June 18, 2019

On this blog we are featuring stories that have been submitted through our website as part of the My Lymphedema Story campaign.  We hope you are as moved and inspired by these stories as we have been. If you would like to share your story, please click on the “Share your lymphedema story” tab on the left […]

Read the full article →

Karissa’s Story

June 18, 2019

  The challenge here is to bring years of lymphedema struggles into a compressed version, so that you can comprehend my journey as a lymphedema patient. How can I explain it? I’ll start at the beginning, when I was 16 years old. After an allergic reaction complete with full body swelling, not all of the […]

Read the full article →

61% Congressional Support!

June 17, 2019

  61% of the members of Congress have already cosponsored the LTA, but 39 Senators and 167 House members have not signed on yet. Persistence is the key to getting their support! Over 7,000 bills have already been introduced in this Congress. Over 600 of them are healthcare bills. Each congressional aide typically handles several […]

Read the full article →

More Opportunities to Connect, Learn, and Advocate!

June 9, 2019

Could you or someone you know use a little LTA 101? We have a brief presentation available as a document or Power Point slides that includes all of the basic, essential information. If you have primary lymphedema you are invited to participate in Rare Across America with the Rare Disease Legislative Advocates group. This is an […]

Read the full article →

The 40 SENATORS who HAVE NOT COSPONSORED

June 3, 2019

If one or both of your Senators are among the 40 who are not yet cosponsoring the LTA please contact their offices this week! ACTION STEPS: 1.) Call his or her office using the phone number and call script here 2.) Send an email using this form 3.) Forward this email and ask others to […]

Read the full article →

Help Raise Awareness

May 30, 2019

This Sunday, June 2nd, is National Cancer Survivors Day. Two-thirds of all cases of lymphedema are cancer-related, and all cancer survivors have a lifelong risk of developing lymphedema. Even if you are not a cancer survivor, you can help raise awareness about lymphedema by writing a letter to the editor about the connection between cancer […]

Read the full article →