The Mighty Logo

I'm Aware That I'm Rare: Danijela Pešić

The most helpful emails in health
Browse our free newsletters

Danijela Pešić is the founder of PH Serbia. She was diagnosed with pulmonary hypertension as a baby over 38 years ago. Danijela is dedicated to raising PH awareness across Serbia and Europe, on behalf of people living with the disease. She works tirelessly to ensure the availability of approved treatments and encourages research for new drugs and therapies. Listen along as she tells her story.


My name is Danijela Pešić and I come from Serbia. We started last year, in 2015. We now have our association less than one year old. It’s a newer association, but we are brave and we want to do many things for patients in Serbia and in the region and every patient in the world.

I am a patient. I have had PH for 38 years, almost all my life. When I was a little baby they told to my parents that I have PH and that it is difficult and I would not survive, but I am long-term survivor. So, I am glad.

My motto is simple. We don’t have any drugs in Serbia, just one in the last two years, and before that, nothing. Many people have PH. Many people die with PH. Nobody is helping us to change something, so we must do that alone. That is the reason for our association. We met the incredible Gerry Fisher. He is a man who has a lot of ideas. We started to learn from him and went to PHA Europe and we are a part of PHA Europe now.

It’s hard to see what’s happening with patients. There are many rare diseases. PH is difficult to diagnose.

We have a few goals. Our first goal is to raise awareness about PH. Last but not least it’s to get drugs, to get treatments. We don’t have treatments. We don’t have anything to live a normal life. It’s quite different when you live with drugs and when you live with treatments for PH and when you live your life without any treatments. That is not a good life.

We have 150 patients. We think that we have many, many more. We organized five events during the 5th of May, World PH Day. Many sportsmen were happy to be with us. That was great. Two soccer teams played in a big derby and 60,000 people watched that and 1.7 million people watched TV via the internet.

We see the changes. We had the opportunity to meet many, many people from other countries, patients, doctors, pharmaceutical companies. We learned many things. We have new contacts. We are trying to do the best for us. Our government, first time in my life, they sent us a letter to go there and see what will be and they want to help us. They see what we doing. Over three million people saw that. Government people saw too. They want to help us.

Many people ask how we approached the sportsmen. It’s a catch. It was very difficult. We had more than 20 meetings with board, with the sportsmen, with many, many people. The key was that we told them that they stay breathless because of wearing the medal. We stay breathless because our award is life. They were touched with that. They want to help us.

I think the next level is better and bigger, trust me. Trust me. We have plans for 2017. We believe that we didn’t do many, many more things. That will come. I hope that patients in Serbia, Bosnia, Macedonia, all Balkan, and all east Europe will get medicines and good treatments and that they will live a good life. That is our goal.

My name is Danijela Pešić and I am aware that I am rare!

Listen to I’m Aware That I’m Rare: the phaware™ podcast at Learn more about pulmonary hypertension at #phaware#phawarepod

Originally published: November 9, 2016
Want more of The Mighty?
You can find even more stories on our Home page. There, you’ll also find thoughts and questions by our community.
Take Me Home