I am japanese 31 year old man.
It was diagnosed as chronic myelomonocytic leukemia in 2014.
I sent a fighting illness life, I took a leave of absence for two years, and I have reinstated.
I experienced anticancer drug therapy, bone marrow transplantation (semi-matched haplo), GVHD.
Occasionally I felt uneasy about the testing / treatment method and GVHD after transplant from a sense of fear.
There are times when I have not slept in the middle of the night and I searched for information on the net till the morning.
However, I could not find any information I wanted.
That is because the method of transplantation and the type of leukemia were minorities.
I will post information that I could not find on this blog.
The reason why I made this blog is to convey my information to the same people or their families for peace of mind.
Please bear with those in painful circumstances
You surely head in a good direction.
2014.4 Blood abnormality is found by medical examination.
2014.10 numerical deterioration of blood → anti-cancer drug treatment .
2015.2 half-match with mother Hapro transplant immunosuppressant .
2015.10 Sacral fracture found Diabetes discovered.
2016.1 Compression of the spine.
2016.3 Cervical spine · Lumbar compression fracture Osteoporosis discovered
2016.11 Sepsis developed.Insulin withdrawal.
2017.1 return to work.
CT, MRI, intestinal examination, lung camera, pulmonary function measurement, malaise, radiation therapy, catheter (laparotomy), radiation therapy, catheter , Peripheral blood stem cell transplantation, bone marrow bank, septicemia, numbness of feet, etc.
I think that there is anxiety which only people who experienced illness understand.
I will take counseling whenever you want.
Even if it is trashy, it does not matter.
It is enough if you can remove even a little anxiety about those who inquired.
Even if it is not a hard text, it does not matter at all.