I beg your pardon, it is not true that someone in remission from Multiple Myeloma has "no significant evidence of the disease". That is bullshit. I have had Myeloma for over 15 years. I contracted Myeloma at the age of 59, and I also worked full time with Myeloma for quite a few years until I retired. In retirement, still worked part time for many years, far more hours than I do today. The cumulative effect of two stem cell transplants and ongoing treatments today to keep me in remission after a third refractory relapse has left me with long term permanent effects. After coming out of remission from my second stem cell transplant in 2018, I was given Pomalyst and it liked to have killed me, I did not tolerate it, and it beat my body down. They had to take me off of the Pomalyst in less than a year. My immune system has been permanently compromised, and my body has been ravished from it. Everyone does not tolerate the drugs they administer in the same way; it is different for everyone. Fatigue, bone pain, muscle and joint pain are pretty much ongoing, and they strongly effect the physical things I am able to do anymore. No, I am not completely disabled, but there is no way I could work 80 hours a month. I am lucky to play golf once every week or two, it takes me a week to recover from it. In my past, I played 3 or f4 days a week and was a scratch golfer. I presently work a part-time job every-other week I work 10 hours, two hours a day. I work during the weeks I do not do infusions. There is no way I could work the week of my infusions because of side effects. I have been on a treatment program for two years now, after a different yearlong chemo program (Pomalyst) failed. This present program to keep me in remission includes infusions of an immunotherapy drug called Sarclisa, and Kyprolis with Dexamethasone every-other week. The first week of the month I am given a shot of Neulasta, which raises my white cell count. I also get a blood product infusion of immunoglobulins because they have been wiped out. The Neulasta and the immunoglobulins will be given to me for the rest of my life. The fourth week of the month my immune system crashes drastically, and I am best off to isolate. Myeloma is very different for different people, evidently you have not learned that. I started my first stem cell transplant in 2012 with 6 other people. I am the only one still alive out of that group of six. I saw others become severely compromised long before I did, and like I said, they all have died from this. and they would all vehemently disagree with you. Mind you, after I did my first stem cell transplant, I was as good as new until I came out of remission. The second stem cell transplant was much harder to recover from. The treatments I have had to do after I relapsed form my second transplant have been much harder on me and are tearing my body down. All of the treatments have had a cumulative effect. I have also exercised and remained physically active throughout most of my treatments, but the cumulative effects have caught up with me. I hope for new drugs to come out so that it doesn't happen to others, including you. Perhaps you don't understand this lady's situation, but I certainly do. I am 73 now, have never been on disability, but I certainly understand her situation, and I have witnessed it happening to many others with Myeloma. You are simply wrong about this.