Reply To: Experience with first Vyvgart treatment – is this normal?

[Community Member]

Hi. I was diagnosed about a year ago after playing round robin with so many doctors over a course of about 7 years with MG symptoms. I had no knowledge of MG prior to my diagnosis. I am curious, I too just finished my first four week round of IV Vyvgart, does anyone else have the LRP4 antibody? If so how are you responding to trx with Vyvgart? My neurologist said not a lot of MG patients with this antibody so we are using the same “toolbox” to trx and hope for the best.