Copper deficiency and MDS with del 5(q) mutation
 

Is there anybody in this forum that has a copper deficiency with MDS? My copper levels keep dropping. I started at 53 received 3 rounds of IV copper chloride and my copper levels went to 54. The doctor says that's nothing in the medical community. My last blood test showed my copper at 48. Magnesium and Zinc was normal. My doctors seem more concerned with the cancer. My low copper is affecting me neurologically. I have seen Chirleys posts and have read a lot of them but I was hoping there is someone that is alive experiencing this same problem. Any insight on care or at home remedies would be fantastic. I was diagnosed with MDS intermediate 3 blasts less than 5%. Looking at getting a stem cell transplant in the near future. Any help with this would be greatly appreciated.