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Amanda Boston

Type of Porphyria

Amanda%20Tshirt.jpgI first saw the opportunity to participate in research studies on the American Porphyria Foundation (APF) Facebook Page.   As soon I as I saw the post I knew I would love to volunteer!  As a young woman in my twenties, I have a vested interest in the race for a cure, and the development of new treatments.  Research studies even help document treatment options that are tried and true in some areas of the country but not others, which is a important in getting insurance companies to consider the treatments normal and standard and therefore a covered expense.  This too is crucial in getting patients treatment.  

I participated in three studies in 2014, the Longitudinal study, the Panhematin Study and the Anylam Study.  The Longitudinal Study required no travel, just some lab work coordinated through my personal physician.  The Panhematin Study involved traveling to the University of Texas Medical Branch (UTMB) in Galveston, TX.   I stayed there five days participated in a double blind study to prove the effectiveness of the IV drug Panhematin.  I already have this treatment available in my area and take it on a routine basis.  However others are not so fortunate and the results of this study will help more people get the treatment prescribed and then covered by insurance.   Then just last week, I went back to UTMB to begin participating in a study for a new drug through Alnylam.   The study involved a physical exam and some lab work, which will be repeated twice more at six months intervals.

All my experiences at UTMB have been positive.  Last week was no exception.  I traveled that morning and arrived at 11am to meet Dr. Anderson, Dr. Ede, and Dr. Hallberg.  Dr. Anderson is very knowledgeable and friendly and I was at ease instantly.  I met him for the first time during the Panhematin study, and he knew what I needed from the moment I walked in.  He had obviously read my medical records and understood Porphyria and understood the symptoms I was experiencing.   He was quick to give me a Panhematin treatment at the onset of an attack and never put my health in jeopardy.  This time I had a simple exam where they took my blood pressure, pulse, temperature, weight and height and then I gave a blood and urine sample.  I flew home the next day, so it was a very small time commitment.

After the research was completed, I met with Desiree Lyon.  She is one of the nicest people I have ever met.  When she speaks about the foundation and research projects, you can truly feel the dedication and commitment.  I admire her strength to cope with Acute Intermittent Porphyria herself while working so hard to help others.    I met some other staff members as well who were friendly and took me out for dinner and made me feel at home and welcome.  The next morning I had asked if I could see more of the work they do at the foundation, and I had the privilege of observing all morning until my flight that afternoon.  I was impressed by the dedication and compassion of the staff!

I know that many people may hesitate to participate in research studies.  I had reservations at first myself, and my fears were quickly put to ease.  The time commitments have been small and the process has been all positive.  I hope this article encourages you to become more involved and participate in finding a cure for Porphyria.

Panhematin Story

Amanda%20Boston(1).jpgI had the most amazing privilege participating in the “7203: A double-blind, randomized, placebo-controlled, parallel group trial on the efficacy and safety of Panhematin® in the treatment of acute attacks of porphyria” research study. I met two amazing Doctors that I had only spoken with through email and telephone: Dr. Karl Anderson and Dr. Akshata Moghe.

The research was performed in Galveston, TX at the UTMB. I was flown into Houston and transported to Galveston. I stayed at the Harbor Hotel until I developed symptoms of an attack, which occurred two days after I arrived, as my attacks are very frequent. For the research, I was blindfolded, the drapes were drawn and foil wrap was put on the cords, so that I wouldn't know if I were getting a placebo or Panhematin™, but my body knows the difference. I was started on the research, but my headaches and abdominal pain was only getting worse. I was about to start an attack. So the rescue treatment, which is Panhematin™, was brought in and administered to me. I felt better the next day. I stand by Panhematin™, and I truly believe that it is an effective treatment for Porphyria.

My whole reason for doing this research was to help others and to show that Panhematin does work. When I first got to the UTMB for the research, I found out that I was the first research patient on this particular study. That is a wonderful privilege. I feel a great sense of accomplishment by participating in the Panhematin research study. I feel that I really accomplished my goal, because I was given the opportunity to help others. I thank the APF for helping me to make my goal a reality. Dr. Anderson is the one who developed and oversaw the research. He is an amazing Doctor and Porphyria expert. He knew exactly what I needed from the moment I walked into the research clinic.   I've never met a Doctor that was so educated on Porphyria and so devoted to the research and helping one’s suffering from Porphyria. Also, he is the nicest person you will ever meet. If anyone with Porphyria has the chance and is thinking about being on a research study, I would suggest that you take that opportunity. It is the greatest privilege you will ever have.