Hello, my name is Anna, I am French, I’m 28, it’s being 2 years and a half that I have blood in the urine with horrible pain.
I had 3 ureteroscopies who have given nothing and now the professor who follows me told me I have the loin pain hematuria syndrome, and there was nothing to do. The only thing I can do is to wait till it’s going better. He refuses to make a biopsy and told me to take aspirin.
I wanted to know if you know doctors who offer other drugs. I've heard of self transplantation and kidney enervation;
I've been in different hospitals and doctors tell me that the pain is bearable and advised me to consult a shrink. I do not think my pain is psychic. I wanted to know if U.S. medical research is more advanced than the French one.
Thank you and good luck
I had 3 ureteroscopies who have given nothing and now the professor who follows me told me I have the loin pain hematuria syndrome, and there was nothing to do. The only thing I can do is to wait till it’s going better. He refuses to make a biopsy and told me to take aspirin.
I wanted to know if you know doctors who offer other drugs. I've heard of self transplantation and kidney enervation;
I've been in different hospitals and doctors tell me that the pain is bearable and advised me to consult a shrink. I do not think my pain is psychic. I wanted to know if U.S. medical research is more advanced than the French one.
Thank you and good luck
Well, the thing is that loin pain hematuria syndrome is a very rare condition and chances are that doctors, even if they do diagnose the syndrome correctly, might not be sure what treatment exactly would be appropriate. But Aspirin somehow doesn't sound right to me - there is a strict warning against the use of Aspirin when there is some sort of the bleeding present. So, it probabbly would be the best that you go and see a pain management specialist, since you have to deal with chronic pain. They will be much more educated to judge what type of painkiller would be most appropriate.
And, from what I've read, self-transplant is usually not very successful - symptoms come back, because no one actually knows what is causing this condition.
And, from what I've read, self-transplant is usually not very successful - symptoms come back, because no one actually knows what is causing this condition.
Can you tell me what are the mental effects from loin pain hematuria syndrome?
Can you tell me something about the physical and mental effects of loin pain hematuria syndrome disorder?