IOCDF Virtual Voices for Mental Health: An Online Day of Action
Virtual Voices for Mental Health program 2021 ASPIRE is again partnering with IOCDF on Virtual Voices for Mental Health program in which we call on our community to contact their...
Getting involved in advocacy is easier than you may think, but it is a critical advocacy effort. We need your help!
Start here: How to Assist with PANS/PANDAS Legislation for lots of fantastic information on getting started, including how to talk to your Legislators and ask for their support. See below for State Pages and additional PANS PANDAS Legislative Resources from ASPIRE. Email the Public Policy Committee today for more information on advocacy efforts in your state!
PANS and PANDAS are severe yet treatable neuroimmune disorders. Despite effective treatments like IVIG and antibiotics, many sufferers are denied care due to the lack of insurance coverage. Families often face an unsurmountable financial strain, leaving some patients without access to appropriate treatment, which can lead to a lifetime of suffering or devastating loss of life. Furthermore, schools absorb a significant financial burden of providing special educational and designated instructional services. Those fortunate enough to receive treatment experience life-changing improvements, as evidenced by survivors who went on to lead successful lives after overcoming PANS. However, the inequity in accessing care persists, leaving most without proper support or understanding. Urgent support is needed to ensure all affected individuals have access to essential medical interventions, enabling them to reclaim their lives and fulfill their potential.
We know that you, the State Leads, are connected to almost everyone in your state, but often, new families find ASPIRE before finding state groups. ASPIRE is here to assist you. We can create State Pages (see below). We will help you share updates and Calls to Action.
For all states working towards passing a bill, ASPIRE has two testimony letters we can update for your state. One is from the Board of Directors, and the other is from the Professional Advisory Board.
What we need from you:
If your state has both a House Bill and a Senate Bill running simultaneously, please let us know how you would like ASPIRE to address the letters with that in mind. Some states want separate letters, while others allow you to include bill numbers and address both House and Senate members in the same letter.
When it comes time to enlist your fellow residents to contact your legislators, we are here to help! We will update Call to Action requests on your state page and help push the information out on our social media.
Virtual Voices for Mental Health program 2021 ASPIRE is again partnering with IOCDF on Virtual Voices for Mental Health program in which we call on our community to contact their...
ASPIRE has signed a letter to Congressman Schrader and Congressman Kinzinger to support the BIOSIM Act. This act would accelerate patient access to new biosimilar treatments by providing a temporary...
WE HAVE A CALL TO ACTION for House Bill #488 that requires insurance coverage for PANDAS/PANS kids in...
Rare Across America Congressional Meetings Make an impact on federal policy from close to your home. Share your rare disease story. Meet other rare disease advocates. ASPIRE joined several...
After you meet with your legislator or one of their staff, please write a brief thank-you note. Make sure to concisely recap your discussion along with what you wish their...
Three laws have been passed to help PANS/PANDAS families with insurance coverage. Named after two of the children of the advocates that drove the legislation, Charlie’s Law of 2017, was...
ASPIRE cosigned the Association for Accessible Medicines’ letter to the FDA urging them to prioritize patient access to more safe, effective, and affordable complex generic medicines in Generic...