Pulmonary Fibrosis

Tiran Chamneni, 57

Living with Pulmonary Fibrosis

My name is Tiran Chamneni, I'm 57 years old, father of two children and grandfather to a new grandchild. For more than 35 years I've worked as a makeup artist and hair designer. A few years ago my life was exactly on the path I'd planned: a successful career, a good relationship, trips abroad, intensive work and many dreams for the future.

And then, one day, it started. During a shower I suddenly felt short of breath. At first I thought it was just a cough or a cold. I took cough syrup, pills — I told myself it would pass. But it didn't.

Gradually I noticed something really wasn't right. I lived on the third floor, and climbing stairs became a major effort. Every few steps I had to stop to catch my breath.

Tiran Chamneni

The Diagnosis

I started undergoing medical tests, and then came the moment when the doctor told me I had a lung disease called IPF — Idiopathic Pulmonary Fibrosis.

I didn't know what that meant. Like many people, I went home and opened "Doctor Google." I read articles, research, explanations. What I saw there frightened me greatly — I understood that this is a disease that progresses over time, and sometimes the only treatment at an advanced stage is lung transplantation.

At that moment I felt my life was over. I sat in the living room and cried. I was certain I wouldn't get to see my children grow up.

"The ability to say 'I'm afraid', 'It's hard', 'I need help' — actually gives real strength."

The Disease in the Closet

But instead of sharing — I chose to hide. I decided to put my disease in the closet.

Because I'm a makeup artist, I knew very well how to create a perfect appearance outward. I kept working, kept smiling, kept showing that everything was normal. But inside I was scared and broken.

I tried to make sure no one heard me coughing. I told everyone it was an allergy. Even when steroid side effects appeared — swelling and weight gain — I found other excuses. And meanwhile, the disease kept progressing. At some point I simply stopped going to appointments. I didn't want to know.

The Flight to Berlin

I continued this way until one day, on a flight to Berlin for a vacation. During the flight I suddenly felt like I had no air. My fingernails started turning blue, and the flight crew gave me oxygen.

From that moment a period of hospitalizations began — in and out of hospitals, until eventually I left one connected to oxygen. And then there was no way to hide anymore. A small plastic tube in my nose did what I'd tried to avoid for years — it took both me and my disease out of the closet.

Coming Out

That moment on the plane was hard, but it was also liberating. When I came out of the closet with my disease, people's reaction surprised me. Instead of rejection, I received acceptance. Friends, family, work colleagues — they all showed me love and support.

I learned that vulnerability is not weakness. The ability to say "I'm afraid", "It's hard", "I need help" — actually gives real strength. Today I take care of myself, I share my story, and I try to help others understand that this isn't something to be ashamed of or hide.

"Vulnerability is strength, and sharing our struggles makes us human."

— Tiran Chamneni

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