| Fortis Healthcare

Le Dr Vikas Dua se rendra à Kinshasa, Congo, en juillet 2024 pour un OPD spécial sur l'hématologie pédiatrique, l'oncologie pédiatrique ainsi que le traitement de l'hématologie, de l'oncologie et des maladies infectieuses pour adultes. Il sera disponible pour sélectionner les patients et fournir des conseils d'expert sur les options de traitement les plus appropriées.

Inscrivez-vous maintenant pour une consultation gratuite

At Fortis Hospital Congo, we understand the complexities and challenges associated with sickle cell disease. With our comprehensive approach to care, we provide advanced treatments and personalized solutions to manage this condition effectively. Our team of experienced hematologists, genetic counselors, and supportive staff are dedicated to improving the quality of life for individuals living with sickle cell disease.

Understanding Sickle Cell Disease:

Sickle cell disease is a genetic blood disorder that affects the shape and function of red blood cells. Individuals with sickle cell disease have abnormal hemoglobin, causing their red blood cells to become rigid and take on a characteristic "sickle" shape. These abnormal cells can cause blockages in blood vessels, leading to pain, organ damage, and other serious complications.

Comprehensive Treatment Approach:

At Fortis Hospital, we offer a multidisciplinary approach to sickle cell treatment, focusing on both managing symptoms and addressing the underlying causes of the disease. Our treatment plans may include:

Medication: We utilize a range of medications to manage pain, prevent complications, and reduce the frequency of sickle cell crises.
Blood Transfusions: In cases of severe anemia or complications, blood transfusions may be necessary to provide relief and improve overall health.
Hydroxyurea Therapy: This medication can help reduce the frequency of pain episodes and complications in some individuals with sickle cell disease.
Bone Marrow Transplant: For select patients, bone marrow transplantation may offer a potential cure for sickle cell disease by replacing diseased bone marrow with healthy donor cells.
Genetic Counseling: Our genetic counselors provide support and education to individuals and families affected by sickle cell disease, helping them understand the inheritance patterns and make informed decisions about family planning.
Lifestyle Management: We offer guidance on healthy lifestyle habits, including proper nutrition, hydration, and avoiding triggers that may exacerbate symptoms.

Why Choose Fortis Gurgaon for Sickle Cell Treatment?

Expertise: Our team of hematologists and specialists are leaders in the field of hematology, with extensive experience in managing sickle cell disease.
State-of-the-Art Facilities: Fortis Hospital in Gurgaon is equipped with advanced diagnostic and treatment facilities, ensuring patients receive the highest quality care.
Compassionate Care: We understand the challenges of living with sickle cell disease and provide compassionate, patient-centered care to support individuals and their families every step of the way.
Collaborative Approach: Our multidisciplinary team works closely with patients to develop personalized treatment plans tailored to their unique needs and goals.
Continued Support: We offer ongoing support and resources to help patients manage their condition effectively and improve their quality of life.

If you or a loved one are living with sickle cell disease, trust Fortis Hospital in Gurgaon for comprehensive, compassionate care. Contact us today to learn more about our sickle cell treatment options and schedule a consultation with one of our specialists. Your journey to better health starts here.

Our Team of Experts

Find us

Read more about FHL-CO-International-OPD-Congo

Fri, 03/01/2024 - 14:10

FAQs

What is sickle cell disease?

Sickle cell disease is a genetic blood disorder that affects the shape and function of red blood cells. People with sickle cell disease have abnormal hemoglobin, causing their red blood cells to become rigid and take on a characteristic "sickle" shape.
What are the symptoms of sickle cell disease?

Common symptoms include pain episodes (also known as crises), fatigue, anemia, jaundice, frequent infections, delayed growth, and vision problems. Complications can vary in severity and may affect various organs and body systems.
How is sickle cell disease diagnosed?

Sickle cell disease is typically diagnosed through blood tests, such as hemoglobin electrophoresis or a sickle cell solubility test. Genetic testing can also confirm the presence of specific gene mutations associated with sickle cell disease.
Is sickle cell disease curable

Currently, there is no cure for sickle cell disease. However, various treatments and management strategies can help alleviate symptoms, prevent complications, and improve quality of life. In some cases, bone marrow transplantation may offer a potential cure.
What treatments are available for sickle cell disease ?

Treatment options may include medications to manage pain and prevent complications, blood transfusions to improve symptoms and prevent organ damage, hydroxyurea therapy to reduce the frequency of pain episodes, and bone marrow transplantation for select patients.
How can I manage sickle cell disease on a day-to-day basis?

Lifestyle management is essential for individuals with sickle cell disease. This may include staying hydrated, eating a nutritious diet, avoiding extreme temperatures, getting regular exercise, and managing stress. It's also important to follow your healthcare provider's recommendations and attend regular check-ups.
Can sickle cell disease be passed down to children?

Sickle cell disease is inherited in an autosomal recessive pattern, meaning that both parents must carry a copy of the abnormal gene for their child to inherit the disease. If both parents are carriers, there is a 25% chance with each pregnancy that their child will have sickle cell disease.
What support resources are available for individuals with sickle cell disease?

Many organizations, support groups, and online communities offer resources, education, and support for individuals and families affected by sickle cell disease. These resources can provide valuable information, connect you with others facing similar challenges, and offer emotional support.
Can adults with sickle cell disease live a normal lifespan?

With proper management and treatment, many adults with sickle cell disease can live relatively normal lives. However, the severity of the disease and the presence of complications can vary greatly among individuals. Regular medical care and adherence to treatment plans are essential for maintaining health and well-being.
Where can I learn more about sickle cell disease?

Your healthcare provider can provide personalized information and guidance based on your specific situation. Additionally, reputable organizations such as the Sickle Cell Disease Association of America (SCDAA) and the Centers for Disease Control and Prevention (CDC) offer comprehensive resources and information about sickle cell disease.

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Dr Vikas Dua (Principal Director - Paediatric Haematology, Haemato Oncology & Bone Marrow Transplant), Fortis Healthcare Limited, India

You can now take free consultation to get all your queries related to below diseases answered –

Sickle cell Anaemia, Aplastic Anaemia, Thalassemia, Acute Leukemia (ALL and AML), Hodgkin lymphoma and non-Hodgkin lymphoma, Immunodeficiencies, Fanconi Anemia, Immune thrombocytopenia, Solid tumors, Neuroblastoma, Rhabdomyosarcoma,Wilms tumor, Osteosarcoma, Ewing sarcom,Brain tumors.

Please note that limited slots are available. So, register immediately on below contact details –

Contact No. - +254 797 777047 / +91 9711674442

Email IDs – [email protected] ; [email protected]

At Fortis Hospital kenya, we understand the complexities and challenges associated with sickle cell disease. With our comprehensive approach to care, we provide advanced treatments and personalized solutions to manage this condition effectively. Our team of experienced hematologists, genetic counselors, and supportive staff are dedicated to improving the quality of life for individuals living with sickle cell disease.

Understanding Sickle Cell Disease:

Comprehensive Treatment Approach:

Medication: We utilize a range of medications to manage pain, prevent complications, and reduce the frequency of sickle cell crises.
Blood Transfusions: In cases of severe anemia or complications, blood transfusions may be necessary to provide relief and improve overall health.
Hydroxyurea Therapy: This medication can help reduce the frequency of pain episodes and complications in some individuals with sickle cell disease.
Bone Marrow Transplant: For select patients, bone marrow transplantation may offer a potential cure for sickle cell disease by replacing diseased bone marrow with healthy donor cells.
Genetic Counseling: Our genetic counselors provide support and education to individuals and families affected by sickle cell disease, helping them understand the inheritance patterns and make informed decisions about family planning.
Lifestyle Management: We offer guidance on healthy lifestyle habits, including proper nutrition, hydration, and avoiding triggers that may exacerbate symptoms.

Why Choose Fortis Gurgaon for Sickle Cell Treatment?

Expertise: Our team of hematologists and specialists are leaders in the field of hematology, with extensive experience in managing sickle cell disease.
State-of-the-Art Facilities: Fortis Hospital in Gurgaon is equipped with advanced diagnostic and treatment facilities, ensuring patients receive the highest quality care.
Compassionate Care: We understand the challenges of living with sickle cell disease and provide compassionate, patient-centered care to support individuals and their families every step of the way.
Collaborative Approach: Our multidisciplinary team works closely with patients to develop personalized treatment plans tailored to their unique needs and goals.
Continued Support: We offer ongoing support and resources to help patients manage their condition effectively and improve their quality of life.

Our Team of Experts

Find us

Read more about Vikas Dua | Kenya | June'2024 | International

Fri, 03/01/2024 - 14:10

FAQs

What is sickle cell disease?

Sickle cell disease is a genetic blood disorder that affects the shape and function of red blood cells. People with sickle cell disease have abnormal hemoglobin, causing their red blood cells to become rigid and take on a characteristic "sickle" shape.
What are the symptoms of sickle cell disease?

Common symptoms include pain episodes (also known as crises), fatigue, anemia, jaundice, frequent infections, delayed growth, and vision problems. Complications can vary in severity and may affect various organs and body systems.
How is sickle cell disease diagnosed?

Sickle cell disease is typically diagnosed through blood tests, such as hemoglobin electrophoresis or a sickle cell solubility test. Genetic testing can also confirm the presence of specific gene mutations associated with sickle cell disease.
Is sickle cell disease curable

Currently, there is no cure for sickle cell disease. However, various treatments and management strategies can help alleviate symptoms, prevent complications, and improve quality of life. In some cases, bone marrow transplantation may offer a potential cure.
What treatments are available for sickle cell disease ?

Treatment options may include medications to manage pain and prevent complications, blood transfusions to improve symptoms and prevent organ damage, hydroxyurea therapy to reduce the frequency of pain episodes, and bone marrow transplantation for select patients.
How can I manage sickle cell disease on a day-to-day basis?

Lifestyle management is essential for individuals with sickle cell disease. This may include staying hydrated, eating a nutritious diet, avoiding extreme temperatures, getting regular exercise, and managing stress. It's also important to follow your healthcare provider's recommendations and attend regular check-ups.
Can sickle cell disease be passed down to children?

Sickle cell disease is inherited in an autosomal recessive pattern, meaning that both parents must carry a copy of the abnormal gene for their child to inherit the disease. If both parents are carriers, there is a 25% chance with each pregnancy that their child will have sickle cell disease.
What support resources are available for individuals with sickle cell disease?

Many organizations, support groups, and online communities offer resources, education, and support for individuals and families affected by sickle cell disease. These resources can provide valuable information, connect you with others facing similar challenges, and offer emotional support.
Can adults with sickle cell disease live a normal lifespan?

With proper management and treatment, many adults with sickle cell disease can live relatively normal lives. However, the severity of the disease and the presence of complications can vary greatly among individuals. Regular medical care and adherence to treatment plans are essential for maintaining health and well-being.
Where can I learn more about sickle cell disease?

Your healthcare provider can provide personalized information and guidance based on your specific situation. Additionally, reputable organizations such as the Sickle Cell Disease Association of America (SCDAA) and the Centers for Disease Control and Prevention (CDC) offer comprehensive resources and information about sickle cell disease.

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Last Name

Mobile Number

Country

Comment

Welcome to Fortis Hospital, Gurgaon: Sickle Cell Treatment

At Fortis Hospital in Gurgaon, we understand the complexities and challenges associated with sickle cell disease. With our comprehensive approach to care, we provide advanced treatments and personalized solutions to manage this condition effectively. Our team of experienced hematologists, genetic counselors, and supportive staff are dedicated to improving the quality of life for individuals living with sickle cell disease.

Understanding Sickle Cell Disease:

Comprehensive Treatment Approach:

Medication: We utilize a range of medications to manage pain, prevent complications, and reduce the frequency of sickle cell crises.
Blood Transfusions: In cases of severe anemia or complications, blood transfusions may be necessary to provide relief and improve overall health.
Hydroxyurea Therapy: This medication can help reduce the frequency of pain episodes and complications in some individuals with sickle cell disease.
Bone Marrow Transplant: For select patients, bone marrow transplantation may offer a potential cure for sickle cell disease by replacing diseased bone marrow with healthy donor cells.
Genetic Counseling: Our genetic counselors provide support and education to individuals and families affected by sickle cell disease, helping them understand the inheritance patterns and make informed decisions about family planning.
Lifestyle Management: We offer guidance on healthy lifestyle habits, including proper nutrition, hydration, and avoiding triggers that may exacerbate symptoms.

Why Choose Fortis Gurgaon for Sickle Cell Treatment?

Expertise: Our team of hematologists and specialists are leaders in the field of hematology, with extensive experience in managing sickle cell disease.
State-of-the-Art Facilities: Fortis Hospital in Gurgaon is equipped with advanced diagnostic and treatment facilities, ensuring patients receive the highest quality care.
Compassionate Care: We understand the challenges of living with sickle cell disease and provide compassionate, patient-centered care to support individuals and their families every step of the way.
Collaborative Approach: Our multidisciplinary team works closely with patients to develop personalized treatment plans tailored to their unique needs and goals.
Continued Support: We offer ongoing support and resources to help patients manage their condition effectively and improve their quality of life.

Our Team of Experts

Find us

Read more about FMRI Sickle Cell

Fri, 03/01/2024 - 14:10

FAQs

What is sickle cell disease?

Sickle cell disease is a genetic blood disorder that affects the shape and function of red blood cells. People with sickle cell disease have abnormal hemoglobin, causing their red blood cells to become rigid and take on a characteristic "sickle" shape.
What are the symptoms of sickle cell disease?

Common symptoms include pain episodes (also known as crises), fatigue, anemia, jaundice, frequent infections, delayed growth, and vision problems. Complications can vary in severity and may affect various organs and body systems.
How is sickle cell disease diagnosed?

Sickle cell disease is typically diagnosed through blood tests, such as hemoglobin electrophoresis or a sickle cell solubility test. Genetic testing can also confirm the presence of specific gene mutations associated with sickle cell disease.
Is sickle cell disease curable

Currently, there is no cure for sickle cell disease. However, various treatments and management strategies can help alleviate symptoms, prevent complications, and improve quality of life. In some cases, bone marrow transplantation may offer a potential cure.
What treatments are available for sickle cell disease ?

Treatment options may include medications to manage pain and prevent complications, blood transfusions to improve symptoms and prevent organ damage, hydroxyurea therapy to reduce the frequency of pain episodes, and bone marrow transplantation for select patients.
How can I manage sickle cell disease on a day-to-day basis?

Lifestyle management is essential for individuals with sickle cell disease. This may include staying hydrated, eating a nutritious diet, avoiding extreme temperatures, getting regular exercise, and managing stress. It's also important to follow your healthcare provider's recommendations and attend regular check-ups.
Can sickle cell disease be passed down to children?

Sickle cell disease is inherited in an autosomal recessive pattern, meaning that both parents must carry a copy of the abnormal gene for their child to inherit the disease. If both parents are carriers, there is a 25% chance with each pregnancy that their child will have sickle cell disease.
What support resources are available for individuals with sickle cell disease?

Many organizations, support groups, and online communities offer resources, education, and support for individuals and families affected by sickle cell disease. These resources can provide valuable information, connect you with others facing similar challenges, and offer emotional support.
Can adults with sickle cell disease live a normal lifespan?

With proper management and treatment, many adults with sickle cell disease can live relatively normal lives. However, the severity of the disease and the presence of complications can vary greatly among individuals. Regular medical care and adherence to treatment plans are essential for maintaining health and well-being.
Where can I learn more about sickle cell disease?

Your healthcare provider can provide personalized information and guidance based on your specific situation. Additionally, reputable organizations such as the Sickle Cell Disease Association of America (SCDAA) and the Centers for Disease Control and Prevention (CDC) offer comprehensive resources and information about sickle cell disease.