Blood transfusion therapy is a crucial treatment for patients grappling with genetic blood disorders such as sickle cell disease and thalassemia.
Every first Thursday of the month, I travel to Raipur for my OPD at Petal's Hospital. During these visits, I see many patients suffering from blood disorders such as Sickle Cell Disease (SCD) and thalassemia
CAR T cell therapy is a form of immunotherapy that harnesses the power of a patient's immune system to combat cancer.
Bone marrow transplant has emerged as a reliable treatment option for millions of children suffering from blood disorders.
My name is Desire Namazzi, and I am 24 years old. I am a resident of Uganda. Today, I am beginning my final year of undergraduate studies
My country, Nigeria, was recently dubbed the “sickle cell capital” of the world. It has the highest number of sickle cell disease cases..
जब भी उसे ब्लड ट्रांसफ्यूजन के लिए अस्पताल ले जाया जाता, तो सुई के डर से वह जोर-जोर से रोने लगती। एक पिता के लिए इससे ज़्यादा दुखद कोई बात नहीं हो सकती कि उसकी बच्ची दर्द में हो और वह कुछ नहीं कर सके।
अक्षत को सिकल सेल एनीमिया के कारण कठिनाइयों का सामना करना पड़ा। सही इलाज, समय पर निर्णय, मदद और उम्मीद ने उनका जीवन बदल दिया। अब वह स्वस्थ होकर सामान्य जीवन जी रहे हैं।
Every year, on May 8, we observe World Thalassemia Day. Its objective is to remind us, medical professionals and other stakeholders, of the resilience of patients living with this genetic blood disorder and the urgency of improving care.
मेरा नाम अखिलेश है। मैं उत्तर प्रदेश के अयोध्या ज़िले के पास एक छोटे से गाँव में कपड़ों की दुकान चलाता हूँ। ज़िंदगी बस किसी तरह चल रही थी। सीमित आमदनी, सीमित ज़रूरतें और छोटे-छोटे सपने थे। लेकिन जब मेरा बेटा अक्षित सिर्फ चार महीने का था और उसका रंग अचानक पीला पड़ गया, वह कमज़ोर हो गया, तब हमारी ज़िंदगी हमेशा के लिए बदल गई।
Just returned from Africa, a continent which bears the highest burden of sickle cell disease in the world.
I still remember holding tiny Joseph in my hands–this fragile, beautiful life that completed us–when the doctors told me he has a dangerous, debilitating disease that can cause him immense pain and suffering growing up.
From the outside, Pari looked like any other child. She had bright eyes, a curious mind, and a voice full of questions. She laughed loudly, ran fast, and talked endlessly about the moon, colors, and her dreams of becoming a teacher one day.
This is my story, and that of my daughter, Rinna. It begins in the early 2000s in the heart of Africa: the Democratic Republic of Congo.It appears that this continent is home to one of the most severe forms of this disease. I was to learn the hard way that it is highly ...
We still remember the day we found out Riona had leukemia. It was September 30, 2022. She was just 10—full of life, stubborn about food, always running around with more energy than we could handle.
I have just returned from Africa, where my days were filled with conversations with children, young adults, and families living under the shadow of sickle cell anemia. What I saw there was more than just a health crisis — it was a human crisis.
Festivals bring families together in joy, celebration, and tradition. But for parents of children living with chronic conditions like Sickle Cell Anemia or Thalassemia, this season can feel overwhelming.
When I first held my daughter Nadeen in my arms, I felt a kind of love I had never known before. She was my first child, a beautiful baby born in Ethiopia, filling our lives with laughter and light. Like any mother, I dreamed of a bright, carefree childhood for her—playgrounds, birthday parties, and the first day of school. But life, as I would learn, had other plans.
I was 17 when my body first whispered that something wasn’t right. I was so tired I couldn’t get out of bed. Not “teenage tired” or “burnt out” tired—this was bone-deep exhaustion that didn’t make sense. I brushed it off, because why wouldn’t I? At that age, illness doesn’t feel like a possibility.