Originally Posted by Mytelase_Alliance

Thank you very much for this information and for sharing your efforts here.

I am just beginning to work on this with my father, who is in need of Mytelase for his MG. We will also be following up with Sanofi directly and will share what we learn here.

The IMD may prove to be the most reliable avenue, so we look forward to hearing more about your effort, and perhaps we can work together on this.

I agree that the Myasthenia Gravis Foundation should get behind this effort with us and help facilitate this process. Let's continue to organize here and together perhaps we can have some leverage with the Foundation to request assistance with this effort.

As you express, there are others such as the elderly who are not able to advocate for themselves. Hopefully our efforts will benefit not only ourselves, but those and others who rely upon this medication. Uniting our efforts, may be the best way to insure access to this critical medicine for us all.