Multiple Myeloma is an incurable blood cancer so you can imagine the bills knowing there’s no cure. I am a patient at MSKCC and they provide great help but it all comes at a cost. I was recently sent a letter from my insurance that the company that makes the medicine for my pain pump has been dropped and that they are probably not going to cover my last months meds, which come to about $4k. Now I can fight them in that but I get stacks of bills every day and have no way to keep up let alone pay. I cannot work because first the cancer but also because I take care of my nonverbal autistic son. Any help would be greatly appreciated and I thank you all.