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New Tool can Measure Disease Activity in Hereditary Angioedema Type 1 and 2

New Tool can Measure Disease Activity in Hereditary Angioedema Type 1 and 2

According to a story from Angioedema News, a team of researchers and scientists have successfully developed a tool that is able to measure disease activity in hereditary angioedema that is…

Continue Reading New Tool can Measure Disease Activity in Hereditary Angioedema Type 1 and 2
‘We Are Visible’ — How Karina Turned Advocacy into Art

‘We Are Visible’ — How Karina Turned Advocacy into Art

'What you can't see can't hurt you.' It's a classic and well-intentioned phrase, but we know it to be quite untrue; especially if you ask any one of the millions…

Continue Reading ‘We Are Visible’ — How Karina Turned Advocacy into Art
One Fibrodysplasia Ossificans Progressiva Trial is on Hold but Another has Shown Promise

One Fibrodysplasia Ossificans Progressiva Trial is on Hold but Another has Shown Promise

Ipsen is a pharmaceutical company based out of Paris. Sadly, they have just announced that they have pressed pause on not one but two studies for fibrodysplasia ossificans progressiva (FOP). FOP…

Continue Reading One Fibrodysplasia Ossificans Progressiva Trial is on Hold but Another has Shown Promise
First Personalized Medicine Trials for Cystic Fibrosis are Underway

First Personalized Medicine Trials for Cystic Fibrosis are Underway

Proteostasis Therapeutics has just announced results from their ex-vivo study of PTI CFTR modulators using organoids from patients living with cystic fibrosis (CF). These organoids are genetically identical, and have…

Continue Reading First Personalized Medicine Trials for Cystic Fibrosis are Underway
Phase 2 Trial for Amyotrophic Lateral Sclerosis has Completed Enrollment

Phase 2 Trial for Amyotrophic Lateral Sclerosis has Completed Enrollment

FightMND is an Australian nonprofit organization dedicated to improving the lives of motor neurone disease patients through funding research for cures. They've successfully provided millions toward research initiatives and clinical…

Continue Reading Phase 2 Trial for Amyotrophic Lateral Sclerosis has Completed Enrollment
A Remarkable Surgery Gives Hope for Babies with Spina Bifida

A Remarkable Surgery Gives Hope for Babies with Spina Bifida

By Rachel Whetstone from In The Cloud Copy When Helisabed Romano was pregnant with her daughter, she got some bad news. The the developing baby had spina bifida, a defect…

Continue Reading A Remarkable Surgery Gives Hope for Babies with Spina Bifida
The Sleepy Road to Diagnosis and Deprivation: A Narcolepsy Patient Story, Part 2

The Sleepy Road to Diagnosis and Deprivation: A Narcolepsy Patient Story, Part 2

This is part two of the story, click here to read part one   After searching for a new neurologist, we found one only 30 mins away that was willing…

Continue Reading The Sleepy Road to Diagnosis and Deprivation: A Narcolepsy Patient Story, Part 2
ICYMI: Newcastle Scientists Identify a Gene that Plays a role in Joubert Syndrome

ICYMI: Newcastle Scientists Identify a Gene that Plays a role in Joubert Syndrome

  According to a recent article in the UK Newcastle Chronicle, when doctors gave Leanne Buckley an opportunity to terminate both her pregnancies, Leanne and her husband Michael were emphatic…

Continue Reading ICYMI: Newcastle Scientists Identify a Gene that Plays a role in Joubert Syndrome
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