N.B.: PLEASE NOTE, THAT ALL THOUGHTS, LINKS AND WORDS BELOW ARE MY OWN, AND DON’T NECESSARILY REFLECT THE OPINIONS OF THE MUSCULAR DYSTROPHY CAMPAIGN / TRAILBLAZERS OR MY WORK WITH THEM.
On Tuesday, I attended the launch of the APPG for Muscular Dystrophy’s Inquiry Report on access to high-cost drugs for rare diseases.
Please click here to read more about the event on my personal blog, which I typed up on Wednesday.
Thoughts? Feedback welcome.
Stay tuned for more updates about the APPG.
By Sulaiman Khan, Trailblazers’ London Regional Ambassador