I was diagnosed with CIDP about 5 months ago. In my case it’s thought to be related to MGUS, a very early form of Multiple Myeloma. My neurologist worked with my oncologist to get my insurance to approve Vyvgart Hytrulo. A nurse comes to my house once a week, to administer subQ and I’ve had 9 doses. Some days I feel like I’m seeing improvement, then other days the pain is unbearable. My neurologist feels there’s a slight improvement in muscle strength but it could be a long road, that I’m willing to travel. I know how lucky I am to be able to receive this medication. For the most part I’m able to continue with daily tasks, just lack endurance. I’ll report back with progress.