Caring Beyond the Cure: How Fatimid Empowers Thalassemia and Hemophilia Patients on a Daily Basis A Commitment for a Lifetime to Saving Lives

 There are thousands of families in Pakistan who wake up every morning with a silent prayer: their thalassemia or hemophilia child receives the medical care they require in order to live one more day. These genetic blood diseases are not short-term conditions—they are lifetime conditions that need ongoing medical care, inner strength, and financial assistance.

At Fatimid Foundation, we recognize that such patients require care far beyond just one transfusion or intervention. It is an ongoing, empathetic process, one we've been privileged to share with our patients for more than four decades.

Understanding the Conditions

What is Thalassemia?

Thalassemia is an inherited condition in which the body fails to produce sufficient healthy red blood cells. Children with thalassemia major, the most extreme form, require blood transfusions every 2 to 3 weeks and consistent thalassemia care in Pakistan to stay alive. They risk organ damage, delayed development, and premature death without ongoing transfusions.

What is Hemophilia?

Hemophilia is a condition where the blood does not have adequate clotting factors. A slight injury may lead to uncontrollable bleeding both internally and externally. Hemophilia patients may have to take injections of clotting factors weekly and in emergency situations such as operations or injuries.

Both diseases are non-curable, but the patients may have long and satisfactory lives with proper treatment.

The Fatimid Difference: More Than Medical Care

At Fatimid Foundation, we don't merely treat—we care for the patient as a whole, in all aspects of their life.

1.  Timely, Safe Blood Transfusions

For individuals with thalassemia, safe and timely transfusions of blood are the key to survival. Fatimid guarantees uninterrupted  thalassemia care in Pakistan:

• All blood is thoroughly tested for HIV, hepatitis B & C, malaria, and syphilis

• Blood is ethically obtained and stored in strict safety guidelines

• Transfusions are done by skilled professionals in clean, patient-centered facilities

2. Hemophilia Clotting Factor Therapy

Replacement of clotting factors is usually costly and difficult to obtain. Fatimid, as a reputed Hemophilia treatment center Pakistan, offers:

• Infusions of Factors VIII and IX, depending on patient requirements

• Emergency intervention for bleeding episodes inside the body

• Patient and family education for home management of hemophilia

3. Diagnostic & Lab Services

Early diagnosis of complications such as iron overload, organ enlargement, and infections can be lifesaving. We provide:

• Routine CBCs, liver function tests, and ferritin levels

• Imaging services and specialist referrals, if needed

• Genetic testing and counseling for at-risk families

4. Holistic Patient Monitoring

Each patient is closely monitored with an individualized care plan. Fatimid keeps:

• Detailed medical records

• Regular health check-ups by experienced doctors

• Follow-up schedules to maintain treatment continuity

Beyond the Clinic: Emotional and Financial Support

Patient and caregiver families tend to be overwhelmed, isolated, and financially burdened. Fatimid offers:

• Counseling services for caregivers and patients

• Nutritional advice to aid in immune and physical health

• Community outreach through patient events and awareness campaigns

• Zakat-funded treatment, rendering therapy fully free for thousands of poor families

The Lifetime Mission of a Patient

Meet Hania, a 9-year-old Hyderabad girl born with thalassemia major. Her parents were heartbroken when they received the diagnosis, with no idea how they would be able to finance lifelong treatment. They discovered the Fatimid—and their lives changed forever.

The last seven years:

Hania gets two transfusions per month

Her blood is screened and maintained regularly

She goes to school and aspires to be a doctor

"Fatimid, the Hemophilia treatment center Pakistan gave us more than medical assistance—they gave us hope," asserts Hania's mother.

The Bigger Picture: A National Challenge

• More than 100,000 patients in Pakistan have thalassemia or hemophilia

• 5,000+ children are born annually with thalassemia major

• 70% of patients do not have access to regular treatment

• Numerous deaths take place due to ignorance and unaffordability

This is not only a family problem—it's a national healthcare challenge. But if we act together, we can turn the numbers around.

How can you help?

• Donate: One rupee at a time. PKR 3,000 can fund a complete transfusion session.

• Give Blood: Blood given safely means lives saved. Drop by your local Fatimid center.

• Sponsor a Patient: Support a child directly for their medical expenses each month.

• Spread Awareness: Inform your loved ones and friends about premarital testing and the value of early diagnosis.

Final Thoughts

For thalassemia and hemophilia patients, survival is a battle—but one that they must not have to battle alone. We accompany them, we nurture them, and we rejoice with them in every step at the Fatimid Foundation.

With your help, we can guarantee no child misses treatment, no parent is ignored, and no life is lost to avoidable suffering.

Become part of our mission. Because care isn't just a treatment—it's a promise.