I hope I spelled it correctly. I know it’s a very rare blood disease.
You stop making white blood cells I know that also.
I hope I got the name right. I had it when I was young, but don’t know what it is. Can’t find anything about it.
please be honest
Rare blood disease and multi organ involvement secondary, neuro problems. Post splenectomy low IgM syndrome progressed damage. No doctor will report my case to the public health as CDC advised if no doctor will treat me. No one will. Att’s say my case is landmark great, after I die. Hospital ER’s refuse admittance even when labs show I should be admitted. Am honest, nice person and doctors often act awful to me. None have taken a complete history and needed, basic tests denied. My illness is child onset, yet some doctors suspect me as causing illness. Doctors deny inpatient hospital eval and some want me in mental unit with no medical workup offered if in mental unit. The damage from untreated sepsis caused diagnosis of drugs that no test confirms cause I didn’t take such drugs. The pseudo drug symptoms caused several wrongful psych holds with proof of no drugs and still denied tests for the neuro damage. I’m at high risk to die. Pre uterine cancer is untreated. Where’s help?