Hi there first time posting. Got diagnosed with Lga Myeloma High Risk February 2024 and been on watch and wait. Just about getting my head around that and told its progressed so had first chemo on 15th May 2025. Have to have it weekly. Going to do 4 months then stem cell transplant then 2 months. Was just wondering if anyone else had gone through this and could give me advice or info. Don't really know what to ask,think or say just kinda on autopilot. Just wanted to see if there was anyone else who had this and could maybe share their experience so I have an idea of what to expect etc and so I could feel not so alone and lost. Thanks
