My story is all too common for patients with autoimmune disease. It starts with misdiagnosis followed by years of tests, infections, minor surgeries, and numerous visits to multiple doctors. I went from being an avid runner and aerobics instructor to having painful, red, and swollen knuckles, reoccurring fatigue, and unexplained fevers. It was five years before I was tested for an autoimmune disease, referred to a rheumatologist, and ultimately diagnosed with rheumatoid arthritis.
I want to share my story because I have learned that my experience is far from unique. As an arthritis and autoimmune disease advocate, I hear stories similar to mine every day. These stories are simply unacceptable, and I have made it my personal goal to ensure that future patients don’t have to go through the same uncertainty and delayed treatment that I went through. Lawmakers must understand the crucial nature of early and appropriate treatment for patients with arthritis and rheumatic diseases. One way to accomplish this dialogue is through attending the ACR’s Advocates for Arthritis fly-in held each September in Washington, D.C.
Advocates for Arthritis provides an opportunity for rheumatology professionals and patients to meet with legislators to not only share our stories, but to speak with them about current legislative issues involving the rheumatology community and to illustrate the impact health policies are having on physicians and patients in their districts and states.
Make a Difference
The first time I attended Advocates for Arthritis, I was a little worried and wondered, “Could I really make a difference?” But, once I got there and was surrounded by other patients with autoimmune diseases like mine—survivors and fighters just like me—who began to share their stories, along with rheumatology professionals, I realized the power that our united voices would bring to Capitol Hill.
The conference is a two-day event. The first day is spent getting to know one another, discussing the current legislative issues at hand and strategizing how we, as a team, would direct our conversations with lawmakers. The following day, our team of patient advocates and rheumatology professionals met with the congressional delegation from our state. It was a truly empowering experience. Here we were—rheumatologists ready to speak on the issues that affect their practices such as billing issues and the need to keep their clinics accessible to new patients, and patients ready to give a “show and tell” to the lawmakers on what it is really like to live with an autoimmune disease day to day, not only dealing with the illness itself, but with the bureaucratic red tape involved in attempting to obtain necessary medications that are out of our financial grasp.
The first appointment was nerve wracking, but I was amazed at how well received we were at every office where we spoke. I attended my second conference in 2011, and was pleased and excited when a few of the legislative members and their aides actually remembered me. It felt good to have built a rapport with them, and to know that I had made a lasting impression.
During last year’s event, I had the opportunity to share my struggles in accessing affordable, quality care with our keynote speaker, Sen. Johnny Isakson of Georgia. Sen. Isakson was so involved in my story that he asked his aide to collect my contact information. After his speech, he came over to shake my hand, and personally asked me to send him my story in writing so that he could use it as real-life example of the difficulties in gaining access to affordable care to share with his colleagues on the powerful Senate Health, Education, Labor, and Pensions Committee. It was such a humbling experience, and I felt honored and encouraged. Lawmakers do hear us and it is critical to continue to engage in these conversations.
These are the types of experiences we need to see more of: more patients and more rheumatologists telling their stories to lawmakers, letting them know that arthritis and rheumatic diseases are crippling, costly, and life threatening, and that, without access to rheumatologists and appropriate treatment, our nation’s healthcare system will be much worse off.
The time for action is now. To make sure that action happens, I know that I’ll keep coming to Advocates for Arthritis every year, talking to my legislators and telling my story and others’ stories, giving lawmakers the facts they need to understand that the pain, disfigurement, and disability from autoimmune diseases are simply unacceptable. I hope to see many new faces, both rheumatologists and patients, during this year’s Advocates for Arthritis event. The ACR is accepting applications now and I hope many of you will take advantage of this important and personally fulfilling opportunity.
Tami Brown is co-founder of the International Autoimmune Arthritis Movement and a dedicated advocate for the rheumatology community.
Now Accepting Applications for Advocates for Arthritis
Apply today to attend Advocates for Arthritis this year on September 10–11 in Washington, D.C. Don’t miss this opportunity to educate Congress on the impact arthritis and rheumatic diseases have on quality of life, and the importance of care provided by a rheumatology professional. The ACR is also looking for patient advocates, so encourage your patients to apply as well. For applications and more information, go to www.rheumatology.org/advocacy.
Can’t travel to Washington, D.C., in September? Sign up to participate in the ACR’s August fly-out. The ACR will arrange an in-district meeting with your lawmaker. Sign up today by contacting Katie Jones at [email protected] or (404) 633-3777.