SAHER FOUNDATION
Saher Welfare Foundation's Lifeline for Children in Need
SAHER FOUNDATION
Saher Welfare Foundation's Lifeline for Children in Need
SAVING LIVES & SPREADING SMILES
Saher Welfare Foundation's Legacy
SAVING LIVES & SPREADING SMILES
Saher Welfare Foundation's Legacy
SAVING LIVES IN AN UNSAFE WORLD
Because every life matters
SAVING LIVES IN AN UNSAFE WORLD
Because every life matters

ABOUT SAHER WELFARE

At Saher Welfare Foundation, we believe in the transformative power of compassion and community. Established with a vision to make a positive impact on the lives of individuals and families, we are dedicated to addressing the pressing needs of our communities, with a focus on [mention specific areas of focus, e.g., healthcare, education, poverty alleviation, etc

WHO WE ARE:

Saher Welfare Foundation, established by Dr. Ghulam Yaseen in 2010 with the idea to save lives and providing hopes. The Saher Welfare Foundation is committed to discover better medications for inherited blood disorders, and it is working for the treatment of children having blood cancers and chronic diseases since 2010. Our main goal is to make our country Cancer free. For this purpose, Saher welfare foundation is educating families to prevent next generations from these hereditary blood disorders. Its projects and activities are made possible by the help and kindness of people, organizations and corporations.

WHAT WE DO:

We are unique in our work, as we treat:

Burkitt’s leukemia is Burkitt’s lymphoma but with the prevalence of malignant Burkitt’s cells in the bone marrow reaching 20%. Burkitt’s lymphoma is an aggressive condition, and it is more common in children than adults

Bernard-Soulier syndrome is a rare inherited blood clotting disorder that is characterized by unusually giant platelet cells, thrombocytopenia, and prolonged bleeding time. Affected individuals tend to bleed excessively and incur spontaneous ecchymoses.

Myelodysplastic syndromes are a group of cancers in which immature blood cells in the bone marrow do not mature or become healthy blood cells. The different types of myelodysplastic syndromes are diagnosed based on certain changes in the blood cells and bone marrow

Pure red cell aplasia (PRCA) is a rare disorder that designates anemia secondary to failure of erythropoiesis. It is characterized by normocytic, normochromic anemia, which is associated with reticulocytopenia in the peripheral blood and absent or infrequent erythroblasts in the bone marrow.

Idiopathic thrombocytopenic purpura is a blood disorder characterized by an abnormal decrease in the number of platelets in the blood. A decrease in platelets can result in easy bruising, bleeding gums, and internal bleeding.

Platelet aggregation: The clumping together of platelets in the blood. Platelet aggregation is part of the sequence of events leading to the formation of a thrombus (clot).

Glanzmann thrombasthenia (GT) is a rare inherited blood clotting (coagulation) disorder characterized by the impaired function of specialized cells (platelets) that are essential for proper blood clotting. Symptoms of this disorder usually include abnormal bleeding, which may be severe.

Acute lymphocytic leukemia (ALL) is a type of cancer of the blood and bone marrow — the spongy tissue inside bones where blood cells are made. The word “acute” in acute lymphocytic leukemia comes from the fact that the disease progresses rapidly and creates immature blood cells, rather than mature ones.

Thalassemia is an inherited (i.e., passed from parents to children through genes) blood disorder caused when the body doesn’t make enough of a protein called hemoglobin, an important part of red blood cells. Thalassemia is a treatable disorder that can be well-managed with blood transfusions and chelation therapy.

Thalassemia is an inherited (i.e., passed from parents to children through genes) blood disorder caused when the body doesn’t make enough of a protein called hemoglobin, an important part of red blood cells. Thalassemia is a treatable disorder that can be well-managed with blood transfusions and chelation therapy.

Hemophilia is usually an inherited bleeding disorder in which the blood does not clot properly. This can lead to spontaneous bleeding as well as bleeding following injuries or surgery. Blood contains many proteins called clotting factors that can help to stop bleeding.

Aplastic anemia is a rare but serious blood condition that occurs when your bone marrow cannot make enough new blood cells for your body to work normally. It can develop quickly or slowly, and it can be mild or serious.

Message of president

Welcome to Saher Welfare Foundation, where we work tirelessly to make a difference in the lives of those affected by thalassemia, hemophilia, blood disorders, and blood cancers. Our mission is to provide access to quality healthcare, raise awareness, offer supportive programs, drive research and innovation, and advocate for policies that benefit patients.

With your support, we can continue this vital work and make a lasting impact. Join us in creating a brighter, healthier future for those in need. Together, we can provide hope and change lives.

Sincerely,
Dr. Ghulam Yaseen
President
Saher Welfare Foundation

OUR PATIENTS

At Saher Welfare Foundation, our ultimate commitment is to the individuals and families we serve. Our patients are at the heart of everything we do, and their well-being is our primary focus. We understand that access to quality healthcare is a fundamental right, and we strive to ensure that no one is left behind. Our patients come from diverse backgrounds and circumstances, each with their own unique stories and challenges. Through our various programs and initiatives, we aim to provide not only medical care but also a sense of hope, dignity, and empowerment. Whether it’s a routine check-up or a specialized treatment, we approach every case with the utmost care and attention.

Burkitt's Leukemia

Burkitt's leukemia is Burkitt's lymphoma but with the prevalence of malignant Burkitt's cells in the bone marrow reaching 20%. Burkitt's lymphoma is an aggressive condition, and it is more common in children than adults

Bernard–Soulier syndrome

Bernard-Soulier syndrome is a rare inherited blood clotting disorder that is characterized by unusually giant platelet cells, thrombocytopenia, and prolonged bleeding time. Affected individuals tend to bleed excessively and incur spontaneous ecchymoses.

Myelodysplastic Syndromes(MDS)

Myelodysplastic syndromes are a group of cancers in which immature blood cells in the bone marrow do not mature or become healthy blood cells. The different types of myelodysplastic syndromes are diagnosed based on certain changes in the blood cells and bone marrow

Pure Red Cell Aplasia

Pure red cell aplasia (PRCA) is a rare disorder that designates anemia secondary to failure of erythropoiesis. It is characterized by normocytic, normochromic anemia, which is associated with reticulocytopenia in the peripheral blood and absent or infrequent erythroblasts in the bone marrow.

Idiopathic Thrombocytopenic Purpura

Idiopathic thrombocytopenic purpura is a blood disorder characterized by an abnormal decrease in the number of platelets in the blood. A decrease in platelets can result in easy bruising, bleeding gums, and internal bleeding.

Thalassemia major

Thalassemia is an inherited (i.e., passed from parents to children through genes) blood disorder caused when the body doesn't make enough of a protein called hemoglobin, an important part of red blood cells. Thalassemia is a treatable disorder that can be well-managed with blood transfusions and chelation therapy.

OUR HAPPY PATIENTS

At Saher Welfare Foundation, the true measure of our success lies in the smiles and stories of our cherished patients. We take immense pride in the joy and gratitude we witness from those whose lives have been touched by our services. These moments of happiness serve as a testament to our unwavering commitment to providing compassionate and quality healthcare. Our patients’ testimonials echo the sentiment of hope and gratitude that permeate our clinics. They speak of regained health, renewed confidence, and a restored sense of normalcy. Their stories are a testament to the dedication of our medical team and the effectiveness of our programs.

OUR TEAM MEMBER'S

Our team’s dedication extends beyond the confines of our organization. Many of our members actively participate in community outreach programs, educational initiatives, and advocacy efforts, amplifying the impact of our collective work. Through collaboration, compassion, and a steadfast commitment to our values, our team members are the driving force behind the positive change we bring to the world. Together, we continue to strive for a more inclusive, empowered, and hopeful future for all.

LATEST EVENTS

At Saher Welfare Foundation, we are committed to creating opportunities for meaningful community engagement and positive social impact. Our latest events have been a testament to this commitment, bringing together individuals, families, and partners to address pressing needs and celebrate the spirit of unity. From our, we witnessed a groundswell of enthusiasm and participation. These events provided platforms for learning, networking, and empowerment. Attendees had the chance to interact with our dedicated team, benefit from specialized services, and connect with like-minded individuals who share a passion for creating positive change.

CONTACT US

We welcome your inquiries, feedback, and collaboration opportunities. Feel free to reach out to us using the following contact details:

Let's Work Together

Email : info@saherfoundation.org

Address: 24 Allama Iqbal Road, Near Railway Cairn Hospital, Lahore. Pakistan. industry.

0302-4853013

    The Saher Welfare Foundation is committed to discover better medications for inherited blood disorders and it is working for the treatment of children having blood cancers and chronic diseases since 2010.

    GET IN TOUCH