At the 2026 MGFA National Patient Conference, Anna Richards, head of commercial at Vitaccess, discusses how the Vitaccess Real MG Registry brings together patient experiences and clinical data to better reflect real world myasthenia gravis care.
Transcript
The Vitaccess Real MG is made in collaboration with the MGFA [Myasthenia Gravis Foundation of America], and we’re building on a legacy of existing patient registry data.
So those 10 years that you’ve already been inputting have been incredibly valuable. We need to take this to the next level.
So by combining patient data and patient experiences and the clinical data, we’ve built up such a holistic picture — the whole picture of how the real-world experience is in MG.
So we’re going to be able to see what clinicians are saying, what patients are saying, and have that complete picture, which was what was missing before.
So we have had elements from both sides, but we don’t want them in silo anymore.
We’re going to bring them both together and really show the real-world picture.
