Save Anas from Gaza – Urgently Needs Lung Transplant
Donate Now
Personal and family photo
Real moments telling the story of my struggle with illness and hope through your support
My Family Is My Strength
Living with pulmonary fibrosis has transformed every detail of my life. Each breath is a challenge, and each day is a new test of patience and endurance. Yet one truth remains unchanged — my family is my greatest source of strength.
They are not just supporters; they are my lifeline. My mother’s constant care, my wife’s unwavering love and patience, and my children’s innocent smiles all give me new reasons to keep going. Their presence always reminds me that I am not facing this illness alone.
This website is not just a place to share my story — it’s a window into how true strength is born from unity, love, and unconditional support. It is a message of hope that life is still possible, as long as family stands by your side.
To everyone visiting this page: Your encouragement, your prayers, and your support make a real difference in my life and the lives of those I love. We are not just confronting illness — we are fighting to reclaim life, breath by breath.
My family is my strength — and with their love, I carry on.
Anas Abu Al-Qumsan
Father of four children from Gaza
"Don't look at the size of the challenges, but at the size of hope that drives us to continue. Each of us has a story, and mine is not over yet."
Glimpses from My Journey
Glimpses from my treatment journey and struggle with lung fibrosis
I never imagined my life would take such a painful turn. It all started by coincidence. I was a young, active man living between dreams and family, until I began experiencing unexplained fatigue and persistent shortness of breath. At first, I dismissed the symptoms, thinking it was just exhaustion or a change in weather, but over time, it became clear that something deeper was wrong.
I never imagined my life would take such a painful turn. It all started by coincidence. I was a young, active man living between dreams and family, until I began experiencing unexplained fatigue and persistent shortness of breath. At first, I dismissed the symptoms, thinking it was just exhaustion or a change in weather, but over time, it became clear that something deeper was wrong.
After undergoing a series of thorough medical tests, the doctor requested that I undergo a Magnetic Resonance Imaging (MRI) scan, along with a Computed Tomography (CT scan). I hoped the results would be minor, but they marked the beginning of facing the hard truth. The scans showed alarming signs, followed by a confirmed diagnosis: Pulmonary Fibrosis.
At first, I couldn't comprehend it. The word "chronic" was enough to change all my plans.
I entered a whirlwind of treatments — medications, oxygen support, and trying to adapt to a new life I had not chosen. I used Corticosteroids, and a drug called Ofev (Nintedanib), which is both rare and expensive, and very difficult to obtain in Gaza.
Despite the illness, I tried to hold on to life. I was fortunate to have my father, who was my true support. He was more than a parent — he was a shadow beside me during every moment of weakness, accompanying me to hospitals, easing my pain with a word, or with a silence I understood deeply.
But war in Gaza spares no one. On a dark day, while my father was out securing necessities for the home, warplanes struck our neighborhood. He was hit by shrapnel from the sudden bombing, and the medics were unable to save him. We received the news in complete shock. We lost the pillar of our family — a man who was more than a father, a companion, and an irreplaceable helper.
His body may have gone, but his spirit remains. His words, his prayers, and every moment he stood beside me live on. His loss did not break me — it made me more determined to carry on.
Amid war, siege, dust, and pain, I learned that life is not measured by breaths, but by the meaning we give to them. And today, as my health grows more complex, and doctors confirm I need a lung transplant, I write these words not as a plea — but as part of the truth.
This is my story. A story of someone who did not choose illness, but chose not to surrender. A story that began in fear, but continues in hope — carrying the legacy of a great man who taught me how to be strong, even in the moment of collapse.
About Me
My journey through life and illness
Personal Information
My Journey with the Disease
It all started gradually... There wasn’t a single moment where I felt my life had turned upside down, but rather a series of small moments: mild shortness of breath, fatigue while climbing stairs, a persistent cough. At first, I thought it was just exhaustion or seasonal allergies. But as time passed, the symptoms worsened, and worry crept into my heart.
I decided to visit a doctor. After some initial tests, I was referred to a pulmonologist. I underwent a Magnetic Resonance Imaging (MRI) scan, followed by a Computed Tomography (CT scan). Not long after, I received the diagnosis that would change my life: Pulmonary Fibrosis.
At first, I didn’t realize the extent of the challenge. A chronic illness that slowly steals my ability to breathe. I began treatment, using Corticosteroids, and was prescribed Ofev – (Nintedanib), a medication that’s difficult to access in Gaza.
I started to adapt — to oxygen tubes, to frequent hospital visits, to a daily life I never imagined. My entire routine changed, but I refused to give up. I fought, driven by the love of my family and an inner hope that never faded.
But the illness wasn’t my only battle. The war made everything worse. The dust from airstrikes, the polluted air, the medicine shortages — all added to the burden. Along the way, I lost my father — my strongest supporter. He was killed in a sudden bombing while trying to secure necessities for us. He left this world carrying my pain with him.
Today, I’m in a critical stage of the illness. Doctors have confirmed that I need a lung transplant, which represents my greatest hope — a hope I can only reach with the support of kind and compassionate hearts.
This is my story... not one of weakness, but of resilience in the face of pain. My journey with illness began suddenly, but it continues with my determination to live, the love of those around me, and an unbreakable spirit.
Impact of the Disease on My Daily Life
The Impact of Pulmonary Fibrosis on Breathing
Breathing — a simple, unconscious act for most — becomes a daily struggle with pulmonary fibrosis. When the lungs are affected by this condition, life changes drastically, and the air that once flowed freely becomes difficult to reach.
What is Pulmonary Fibrosis?
Pulmonary fibrosis is a disease that scars and thickens the tissue in the lungs, making it increasingly difficult for them to transfer oxygen into the bloodstream. Over time, this reduces lung function and makes breathing a constant effort, even while at rest.
How does it affect breathing?
- Shortness of breath with even minimal activity, such as walking or talking.
- Increased heart rate due to low oxygen levels.
- Dependence on supplemental oxygen to support lung function.
- Overall fatigue due to inadequate oxygen supply to the body.
Daily life impact:
- Simple activities like climbing stairs or getting dressed become exhausting.
- Sleep is disrupted, especially when oxygen is needed overnight.
- A sense of helplessness can develop, often leading to emotional and mental strain.
Pulmonary fibrosis doesn’t just affect the lungs — it weighs heavily on every breath, every step, and every moment of daily life. But it also gives a new perspective on existence... where each breath taken is an achievement, and each day lived is a gift.
That’s why your support is not only for treatment, but for a renewed chance at life.
The Impact of Pulmonary Fibrosis on Mobility
Moving is no longer automatic. With pulmonary fibrosis, every movement becomes a calculated effort of energy and oxygen. Patients often feel as though their bodies are heavier than their ability to carry them.
How does pulmonary fibrosis affect mobility?
- Shortness of breath with any exertion: Even walking a few steps can cause severe breathlessness and fatigue.
- Oxygen deficiency: Muscles don’t receive enough oxygen, leading to weakness and reduced movement capacity.
- Dependence on portable oxygen: Many patients need to carry oxygen equipment, making movement both physically and mentally exhausting.
- Muscle mass loss: Due to reduced physical activity and poor nutrition, muscle atrophy can occur, further limiting mobility.
Daily life impact:
- Climbing stairs, moving around the house, or even standing for extended periods becomes a challenge.
- Patients often require assistance, affecting their sense of independence.
- Social participation declines, as physical effort becomes overwhelming.
Yet despite these limitations, the human will remains strong. Many patients, despite their suffering, push themselves to maintain a minimum level of activity to avoid further deterioration. They prove every day that while the body may weaken, the spirit does not give in.
Every step taken with pulmonary fibrosis is a battle — and the victory lies not in speed, but in determination.
The Impact of Pulmonary Fibrosis on Work
Work is not just a means of earning a living — it’s a source of identity, purpose, and a sense of contribution. But when a person is diagnosed with pulmonary fibrosis, their relationship with work begins to change gradually.
How does pulmonary fibrosis affect the ability to work?
- Chronic fatigue: Persistent shortness of breath and ongoing exhaustion make it hard to concentrate or maintain daily tasks.
- Frequent need for rest: The patient requires regular breaks, which can conflict with fast-paced work environments.
- Dependence on oxygen therapy: Carrying oxygen equipment may limit mobility in the workplace.
- Frequent medical appointments: The condition often requires regular hospital visits and check-ups, leading to increased absenteeism.
Psychological impact:
- Patients may feel guilty toward coworkers or employers, adding emotional strain.
- Self-esteem can decline due to the loss of productivity or inability to perform as before.
Possible solutions:
- Transition to remote work or flexible roles that can be done from home.
- Reducing working hours or modifying job duties to align with physical capacity.
- Supportive workplaces that accommodate medical needs and foster understanding.
In summary:
Pulmonary fibrosis doesn’t only weaken the body — it can also take away a person’s livelihood and sense of purpose. That’s why social and professional support plays a vital role in helping patients maintain dignity and continuity in life.
Because work isn’t only what we do — it’s also how we see ourselves.
The Impact of Pulmonary Fibrosis on Family
When a loved one is diagnosed with a chronic illness like pulmonary fibrosis, the effect isn’t limited to the patient alone — it extends deeply to the entire family. The household becomes a constant support system, roles shift, and priorities change.
How does pulmonary fibrosis affect the family?
- Emotional strain: Family members often live in constant worry about the patient’s health and fear of deterioration or an uncertain future.
- Emotional strain: Family members often live in constant worry about the patient’s health and fear of deterioration or an uncertain future.
- Financial burden: The high cost of medications such as Ofev (Nintedanib) and oxygen therapy can place a heavy strain on the family's finances.
- Social impact: Families may reduce social engagements or withdraw from the community due to caregiving responsibilities.
Impact on children:
- Children may feel confused or anxious if the situation isn’t explained appropriately.
- Some may take on responsibilities beyond their age to help support the household.
On the other hand:
- Illness can strengthen family bonds, making love and sacrifice more visible.
- Family members grow together, learning patience, compassion, and deeper values.
In summary:
Pulmonary fibrosis places its weight on the whole family, but it also reveals their true resilience. Every moment of care, every shared burden, is proof that family is stronger than illness.
Illness may weaken the body, but it elevates the hearts that love unconditionally.
Why I Need Your Support
The cost of a lung transplant abroad is far beyond what my family and I can afford. It includes surgery, travel, accommodation, and long-term care. Your support is my only hope to survive.
Some journeys in life are not chosen — they are imposed. My journey with pulmonary fibrosis is one of them. It’s a daily battle that affects my ability to breathe, move, work, and live even the simplest parts of life. Despite the heavy burden, I hold on to hope — the hope that kindness still exists and that support can transform pain into life.
My Health Condition
Pulmonary fibrosis is a chronic and progressive disease that scars the lungs. Every breath becomes harder than the one before. Today, I rely on oxygen therapy and take expensive medications like Ofev (Nintedanib), and I require constant medical supervision. My condition has reached a critical stage, and doctors have recommended a lung transplant as the only life-saving option.
The Financial Challenge
- The transplant surgery is extremely expensive and not available in Gaza.
- The medications are rare and costly, and often unavailable due to the blockade.
- Ongoing care includes oxygen equipment, hospital visits, and post-transplant treatment — all of which are financially overwhelming.
What Your Support Means
Your support is not just financial aid — it’s a lifeline. It’s a chance for me to breathe again, to continue being a father, a son, and a human being with dreams and responsibilities.
By supporting me, you are:
- Helping me access critical medical care
- Allowing me to continue fighting for my life with dignity
- Giving hope to a family that refuses to give up
That’s why your support is not only for treatment, but for a renewed chance at life.
Estimated Total (First Year)
Item
Operation and examinations
Travel & Accommodation
Post-Surgery Care
Total
Donation Counter
Required
Donated
Remaining
Support My Journey – Donation Information
If you feel moved by my story and wish to stand beside me in this critical stage of my treatment journey, your support can make a real difference.
Financial Support
Direct financial donations are the fastest way to help cover the cost of treatment
Bank Transfer
Direct transfer to the treatment bank account
Other Ways to Help
You can contribute to saving my life in many non-financial ways
Contact Organizations
Reach out to health and humanitarian organizations that might offer assistance
Moral Support
Messages of encouragement and moral support give me strength to continue the fight