For information and/or questions about Advocacy and Public policy please contact:
Bill Murphy, Director, Advocacy and Public Policy

(617) 851-7585
wmurphy@epilepsynewengland.org

ADVOCACY

Epilepsy Foundation New England is committed to protecting the rights of people with epilepsy and ensuring that they have access to needed treatments and services. We do this by helping individuals and also by advocating with our elected officials, community leaders and policymakers. To make sure you stay up to date on our activities, and lend your voice, we invite you to join our Speak Up Speak Out network of advocates.

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HAPPENING SOON

DID YOU KNOW… health insurance plans are often switching or not covering the medications of many patients with complex, chronic conditions (including epilepsy) for non-medical reasons. This is known as “non-medical switching” and it can lead to a serious, even fatal, situation if folks don’t get the medications they need. Has your medication been switched without your and/ or your doctor’s permission?  Have you had problems because of it? If so, we would like to hear from you and invite you to join us for an important meeting of the Massachusetts’ Commission to Study Switching Medications:

Listening Session
Monday, November 13, 2017
5-7 PM
Health Policy Commission
50 Milk Street 8th Floor
Boston, MA

EFNE played an important role in encouraging the state to look at this important issue and to create the Massachusetts’ Commission to Study Switching Medications. Now, it is crucial that the Commission members hear from patients. If you would like to participate and/or share your story please contact Bill Murphy at wmurphy@epilepsynewengland.org  

 Visit here for more information on the Commission and this special meeting.

 

HOT TOPICS!   TAKE ACTION NOW!

SIGN THE PETITION TO REFORM STEP THERAPY:  Step Therapy, also known as Fail First, happens when a health insurance company forces a patient to try and fail on medications other than what their doctor prescribed, before they will cover the cost of the original prescription.   Delays in care can have serious medical consequences, adds extra visits to the doctor's office and ultimately can drive up overall health care costs.  Doctors know what to prescribe and know their patients best.   Their medical expertise should not be overturned by insurance companies looking to save money while jeopardizing the health of patients. Has this happened to you?  We currently have important bills before the Massachusetts Legislature to make sure people get the medications they need.  You can help us tell legislators how important this is by taking this survey and  by telling  your legislator you want to reform this discriminatory practice!

 

STAY INFORMED

Find out what’s happening in your state:  Maine  Massachusetts  New Hampshire  Rhode Island

Visit this page for the latest advocacy news from the national Epilepsy Foundation.

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For information and/or questions about Advocacy and Public policy please contact:
Bill Murphy,
Director, Advocacy and Public Policy
Phone: 617 (506) 6041 x 104
wmurphy@epilepsynewengland.org