In April, the Ministry of Health announced that it has given the “orphan medicine” status to Koselugo, a prescription drug used in treating children with neurofibromatosis type 1 and the only medical treatment that is available for this rare disorder. With May being Neurofibromatosis Awareness Month, we discuss what the availability of this treatment means for children with neurofibromatosis and the gaps that still remain, together with Prof Dr Thong Meow Keong, consultant paediatrician & clinical geneticist, and Carol Lim, who is living with neurofibromatosis.

Produced by: Lim Sue Ann

Presented by: Tee Shiao Eek

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Categories:  health policy,  wellness,  managing disease,  medical advances

Tags:  koselugo,  selumetinib,  schwannomatosis,  tumour,  nerves,  rare disease,  rare disorder,