Tuesday, May 7, 2013
Clara Hauke EPP!
Type of Porphyria:
Erythropoietic Protoporphyria (EPP)
I’m 18 years old and have experienced pain after staying in the sun since I was about 2 years old. When I was 2, I was outside and all of the sudden I started crying. Nobody knew why and my parents asked themselves whether or not I was pretending. Slowly they figured it had to do with the sun. We tried so many things and we went from doctor to doctor, but nobody had a clue what exactly my problem was. Several times my eyes were so swollen I couldn’t see anything. In the summer it was horrible. At night I couldn’t sleep, I itched myself until I was bloody – awake or sleeping. The only solution for me was to protect myself and to stay out of the sun. But I didn’t want to be different from my friends and I didn’t want to be a burden for my family. So I often crossed the border, to make it possible for my family to take me with them.
When I was about six or seven, I met a doctor by chance, who guessed what my problem was. She sent me to a university hospital, where my family and I got a diagnosis: Erythropoietic Protoporphyria. Just this fact helped us a lot.
For a long time I thought I was the only one having this stupid problem. But then my mother found a support group for German EPP patients. We went to a meeting and it was so strange hearing people talk about things I experienced as well. My family supports me a lot but they can’t understand me like someone with EPP is able to. Just simply talking with someone so similar was great. I got to know a girl about the same age as I am and we became very good friends. Last year we spent two weeks in Greece. During day we stayed inside or in the shade and in the late afternoon we lay on the beach.
Growing older I got to know my limit. Now being more responsible for myself, I have to measure the fun and the pain I likely will have when I do any outdoor activity. By now I’m so self-comfortable that I don’t feel strange anymore wearing my huge hat and long sleeve. I try to avoid taking pain killers, but sometimes it’s inevitable even though I protect myself.
EPP of course limits me in certain ways, but sometimes I don’t care. Having an awesome day downhill skiing, a class trip to Rome (all day sunny, 42°C the time I was there) or having fun at a bike-tour with friends is worth having any pain.
Remember….. Research is the key to your cure!
Type of Porphyria: Acute Intermittent Porphyria (AIP) Sive Ngalo of Ekasi Hub interviewed Athi Koti. Below is my story ...
Erythropoietic Protoporphyria What is erythropoietic protoporphyria? The word ‘erythropoietic’ means associated with red blood cells (‘...
Happy Thanksgiving everyone 2017
#PAW2018 This year, each day we will bring you a member story of each type, a Medical Fact on each type, Medications approved ...