An IPPF News Site

  • Advocacy in Action

    You may be aware of the IPPF’s advocacy efforts. Now, we need you to advocate, too. Your story is important and shows that rare disease not only affects Americans, but Americans in your district. Your story proves to congressional members that their decisions have a great impact on human life and well-being.

  • Advocating for Dental Research

    The IPPF had the pleasure of interviewing Lindsey Horan, AADR’s Assistant Director of Government Affairs about their 2018 Advocacy Day and important legislative issues.

  • In-District Lobby Days

    For the past four years, I have joined IPPF patients and others in the rare disease community across the country in advocating to congressional members in my district. The IPPF is joining forces again this year with Rare Disease Legislative Advocates (RDLA) for In-District Lobby Days from August 7, 2017 through September 6, 2017.

  • Rare Disease Day 2017

    Rare Disease Day is a day of unity for us patients with rare diseases. I can’t speak for you, but I felt very alone and isolated when I found out I had pemphigus vulgaris. Then I found community in the IPPF. It was very comforting to know there were others out there who had gone ...

  • Rare Disease Patients Need 21st Century Cures Now

    Although there has been a huge public outcry over the cost of prescription drugs, there has been little public discussion about the need for innovation for patients who don’t yet have an effective therapy. It is estimated that 1 in 10 Americans suffer from a rare disease, and only 5% of rare diseases have a ...

  • Rally for Medical Research

    In addition to our general request for NIH funding, I stressed the importance of cutting edge research on rare diseases and emphasized the significance of the Open Act, which incentivizes pharmaceutical companies to make treatments available off-label.

  • Why Advocacy?

    Since its inception, the IPPF has had a strong commitment to advocacy. Our goal has been to promote favorable government policies to create awareness and accelerate the pace of scientific discovery for pemphigus and pemphigoid.

  • Join the IPPF to Ensure the Rare Disease Community is Heard This Summer

    During the summer recess, Congress returns to their home states to hear from constituents and attend community events. Meeting with them during this time is a critical opportunity for rare disease advocates to build relationships, educate them on key legislative needs, and follow-up on requests made during Rare Disease Week on Capitol Hill or phone ...

  • Speak Up, Stand Up, Write Up, and Talk Up

    When there was an opportunity to be an advocate, Marc suggested that I attend Rare Disease Week in Washington, DC. My first reaction was FEAR. The walking, my body aching, standing were just a few of my worries. EXCITEMENT was the next emotion. There would be stories that I could relate to and new people ...

  • Advocating for Change: Home Infusion Therapy

    As we shared our stories on behalf of the entire P/P community, I could see that many of the legislators’ offices we visited began to understand the dilemma. However, it was clear this issue would take an effort by the entire P/P community for our voices to be heard.