Our House cosponsor count is now at 92! However, although it is only the beginning of October there is very little work time left in this Congress. To reach our goal of at least 100 cosponsors by years end we cannot let up!
Click HERE and then on “cosponsors” to see if your Representative is a cosponsor. If he/she is not, please click HERE to use our submission form with template letter. Or, if you would like to submit a completely custom letter click HERE for instructions. If you have written before and your Representative still hasn’t cosponsored then a custom letter is a great option!
Contacting your members of Congress and securing their cosponsorship is a priority, but these are other ways you can support passage of the Lymphedema Treatment Act:
* Refer a friend to our website with our easy Tell-A-Friend form
* Add our widget/plugin to your website or blog
* Distribute our flyer or information cards
* Visit our Cafe Press store
* Sign our change.org petition
* Write the Department of HHS
* Share your lymphedema story
* Write the media (contact info provided)
* Donate financial support (PayPal accepted)
* Participate in our next advocacy trip to DC (spring of 2013)
Thanks for your continued support!
Heather Ferguson
Executive Director, Lymphedema Advocacy Group
www.LymphedemaTreatmentAct.org
info@LymphedemaTreatmentAct.org
