The official information is that there is no cure. I could read about the odd case that went into remission, but that seems to be more the exception than the rule. Several of those cases needed bone… read more
I have secondary Myelofibrosis. I take Jakafi 10 and Anagrelide.05
Twice a day. My numbers are good.
This definition is from the Cleveland Clinic:
There are two types of myelofibrosis:
Primary myelofibrosis is myelofibrosis that occurs on its own.
Secondary myelofibrosis arises secondary to other… read more
Please anyone can help me with an online consultation with a suggested hematologist so that i can confirm my brother's diagnosis, as two hematologists said the diagnosis is polyvythemia vera, while my current hematologist said it is prefibrotic myelofibrosis. I am so anxious.
Note: i can pay the fee of consultation to the suggested hematologist
Thank you for your answers, he was good for 2 months post therapy, now again he feels fatigue, abdominal pain, pain in jaws and face, though the lab findigs are excellent. We are fron iraq, and there… read more
Thank you, Tatiana!
You are so knowledgeable. I asked my specialist at a recent appointment Whether my percent of mutated alleles that are JAK2 positive Have any correlation to the severity of my… read more
I was diagnosed with Polycythemia Vera in Jan 2024.
I receive disability for multiple conditions
Currently I am being treated with low dose Aspirin. Other than that, there is no medication at all. If anyone has the same condition as me and is being treated, please give me more information. Thank you very much
Hello BichDiem
I'm glad you're here and getting good information from Steve and others on this site. I'm also glad to here that you have an appointment this month to learn more from an expert
To… read more
As far as one can read, it cannot. MPNs (ET, PV, MF, unspecified) do not behave like solid tumour cancers that can metastasise to other organs
MPNs might be secondary to other cancers, mostly as the… read more
I have ET/JAK2 mutation.
Yayyyy. You go, girl!!!
Platelets at 87,000. Enlarged spleen. I am wondering if anyone out there has Myelofibrosis and what treatment they are currently undergoing?
I am early stage (2yrs.). No symptoms yet and no meds. Only had several phlebotomy. My numbers are getting in control very soon. Good luck!!