Spread the word & distribute this flier
HELP US GET THE WORD OUT!
This is an entirely patient-driven, grassroots cause. We have no paid lobbyists and are not represented by any special interest group. Our continued progress depends on the involvement of more people just like you.
Please help increase awareness of the bill in the following ways:
- By verbally sharing information about the bill with your doctors, therapists, support groups, family members and anyone interested in this legislation – encourage them to visit this website for more information.
- By posting information about the bill and this website on social media networks and blog sites you visit.
- By printing and distributing this one-page informational flier (for Spanish version click here) to patients with or at risk for lymphedema, and at your doctors, therapist and compression garment fitter’s offices. Ask these care providers to display copies in their offices or make copies available for patients to take. Alternatively, if you are unable to print this flier yourself, we can mail you information cards (seen below) to hand out. Just contact us with your request and the number of information cards you need.
- By placing the Lymphedema Treatment Act Logo and/or this Lymphedema Treatment Act Information Card (below) on your website as a link to this website. If you would like either of these images emailed to you directly please Contact Us.
