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How do I know if I have Myelofibrosis?

What signs or symptoms may make you suspect you may have Myelofibrosis. People who have experience in Myelofibrosis offer advice of what things may make you suspicious and which doctor you should go to to receive treatment

Do I have Myelofibrosis?

Myelofibrosis is a rare and chronic bone marrow disorder characterized by the abnormal production and accumulation of fibrous tissue in the bone marrow. This condition disrupts the normal production of blood cells, leading to various symptoms and complications.



Diagnosing myelofibrosis requires a comprehensive evaluation by a healthcare professional, as the symptoms can be similar to other conditions. Here are some key indicators that may suggest the presence of myelofibrosis:



1. Symptoms: Myelofibrosis can cause a range of symptoms, including fatigue, weakness, shortness of breath, unexplained weight loss, night sweats, and bone pain. These symptoms may develop gradually and worsen over time.



2. Enlarged Spleen: One of the hallmark signs of myelofibrosis is an enlarged spleen (splenomegaly). The spleen may become enlarged as it tries to compensate for the decreased production of blood cells in the bone marrow. This can cause discomfort or pain in the left upper abdomen.



3. Anemia and Abnormal Blood Counts: Myelofibrosis can lead to anemia, a condition characterized by a low red blood cell count. Additionally, it may cause abnormal levels of other blood cells, such as low platelet count (thrombocytopenia) or high white blood cell count (leukocytosis).



4. Bone Marrow Biopsy: A definitive diagnosis of myelofibrosis is typically made through a bone marrow biopsy. This procedure involves extracting a small sample of bone marrow from the hipbone or another site and examining it under a microscope to assess the presence of fibrosis and abnormal cell growth.



5. Genetic Testing: Certain genetic mutations, such as JAK2, CALR, or MPL, are commonly associated with myelofibrosis. Genetic testing can help identify these mutations, aiding in the diagnosis and classification of the disease.



If you are experiencing any of the symptoms mentioned above or have concerns about myelofibrosis, it is crucial to consult with a healthcare professional. They will evaluate your medical history, perform a physical examination, order relevant tests, and provide an accurate diagnosis.


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Stories of Myelofibrosis

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I was recently told I have myelofbrosis (6-28-16) and so far I'm flying blind. I don't know what stage I'm at, nor do I know how longI've had this, but I have an appt. with my onocoligist on 7-14-16 and that is going to be one of my first questions. ...

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