APPG for Muscular Dystrophy’s Inquiry Report Launch on access to drugs for rare diseases

Published Date
06/09/2013
Author

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.

APPG Inquiry Report into accessing rare disease drugs

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

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