Hi all, My husband is 59. He was diagnosed with MM two years ago. He had stem cell transplant that lasted 4 months. He then had car-t that lasted 5 months. Last week, he went into the hospital and had a new treatment with Taquilamed. Out of all the treatments, Taquilamecd was the absolute hardest. I pray this lasts longer than the others. Had anyone else received the Taquilamed shots? He had so much pain and swelling. It was brutal on his body.