The robust processes to evaluate applications to n-Lorem’s nano-rare patient treatments.
All tagged nano rare disease
The robust processes to evaluate applications to n-Lorem’s nano-rare patient treatments.
Podcast host and rare disease advocate, Effie Parks, chats about her son Ford who has CTNNB1 Syndrome.
First episode of the N-Lorem Foundations’ “Patient Empowerment Program” features an actor turned patient advocate and a pediatric geneticist.