UnifyRare is your resource for accessing information about the rare diseases Alexion studies and to learn how our pioneering treatments are building a better future for people with rare diseases
gMG
Generalised myasthenia gravis
NMOSD
Neuromyelitis optica spectrum disorder
aHUS
Atypical haemolytic uraemic syndrome
NF1
Neurofibromatosis type 1
HPP
Hypophosphatasia
CLINICAL CHARACTERISTICS
Learn more about the rare diseases we treat and how to recognise and best care for patients in your clinical practice
PRODUCT INFORMATION
Explore details about Alexion products available to treat rare diseases
EVENT REGISTRATION
Access and register for our educational webinars and symposia
RESOURCES
Find a library of resources available to support you and your patients with rare disease
Stay informed on new educational updates in your area of interest, our latest symposia, and to register for our webinars and other events.
Watch our video series highlighting the impact of living with a rare disease:
healthcare professional
Meet Lelainia Lloyd, a resident of British Columbia, Canada, a new grandmother to three grandchildren, a mixed media artist, podcaster, and wheelchair curler. Lelainia is also a busy activist, sharing her experience as a person living with NMOSD, the impact on her day-to-day life, and how she has faced the challenges of her disease.
gMG, generalised myasthenia gravis; HPP, hypophosphatasia; NF1, neurofibromatosis type 1; NMOSD, neuromyelitis optica spectrum disorder.