Our Inspiration
- Living With Rare Diseases
- Real Stories
  - NF1
  - aHUS
  - gMG
  - HPP
  - LAL-D
  - NMOSD
  - PNH
- Support Services
Albie, one of our guiding stars

When Albie was born, his mom, Charlotte, said that he was “absolutely fine. Everything was fine for about two weeks.”
Our Medicines
- Conditions We Treat
  - aHUS
  - gMG
  - HPP
  - LAL-D
  - NF1 PN
  - NMOSD
  - PNH
- Medicines
Our medicines help people like Donnan

As a father of two young children, Donnan recalls being afraid of what the future would hold prior to his diagnosis.
Our Research
We innovate for Ruthie

Married with a newborn son, Ruthie was scared to learn that PNH was a life-threatening illness that at the time had no approved treatment.
Our Commitment
We give back for families like Evie's

At only three months old, Evie's parents were told that her case was severe and that there were no approved or effective treatment options.
Our Company
Liz is our inspiration

Although physical challenges required Liz, her husband, and their children to adjust their lives in many ways, she doesn't let her disease hold her back.
Your Career
- Career Opportunities
  - Join Our Team
- Working Here
  - Benefits
  - Culture
Make a difference for families like Tristan's

Tristan's parents experienced a whirlwind of emotions and fear after learning their 5-year-old son had such a rare and serious disease.

LIZ
LIVING WITH gMG

REAL STORIES

Real Stories of Living With gMG

Aimee

Diagnosed with gMG

In her 30s, Aimee began to experience several unusual symptoms. It started with a droopy eyelid and progressed to episodes of choking while eating or drinking.

HEAR HER STORY

Liz

Diagnosed with gMG

When Liz was in her 30s, she started to notice that she was having trouble seeing. Soon after, she began to experience weakness in both her arms and legs.

HEAR HER STORY

Discover how we’re serving people living with gMG

gMG MEDICINE

See how we’re pushing the boundaries of gMG research every day

PIPELINE

Real Stories of Living With gMG

Aimee

Diagnosed with gMG

Liz

Diagnosed with gMG

Discover how we’re serving people living with gMG

See how we’re pushing the boundaries of gMG research every day

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