I really admire the way people from the UK share their experiences openly here on You Tube , thank you so much. I learn most of my research through the people of the UK and it really helps me to see how lacking our health care system can be here in Ontario. Doctors here don't seem to want to talk about the a lot of the Rare Diseases that they are overlooking and thanks to the Internet we are learning for ourselves.
I’m being checked for MM - I dispensed petrol and paraffin for a couple of years when I was 15 - and was an air stewardess on early morning flights where fuel was always being loaded onto our HS 748s. It will be interesting if I do have it because I have never heard of the petrochemical connection.
WHATS correlation between m spike level and plasma cell percent.do new mgus pateints need bone marror biopsy>? my mgus myeloma specialist hasnt said i need one unless i had symptoms? and i read somewere m sike of 1.5 g/DL correlates with plasma cell over 10 %
I'm shocked that they would give you medicine that would be harmful to your kidney function is your kidney function is already at risk with the cancer. I'm guessing that most people who have multiple myeloma end up needing a kidney transplant but I'm wondering who's fault that is
