Breathe With Me

Breathe With Me is a social media community group trying to raise funds for cystic fibrosis research by focusing on outreach to the non-CF community. The group leads its campaigns by asking the general public to “try breathing like a person with cystic fibrosis.”

Condition Awareness & Advocacy

Here is a list of conditions this partner raises awareness and advocacy for:

Resources & Support

Homepage

About

Donate

Connect With Breathe With Me

Patient Worthy Posts on Cystic Fibrosis

NanoPODS: A New Way to Effectively Deliver Treatment in Cystic Fibrosis?

The Problem One of the greatest challenges in the investigation of nanoscale treatments for people with rare diseases is figuring out how to administer the

Cystic Fibrosis Hearing Loss Drug Aims for Phase 2 this Summer

According to an article from Pharmaceutical Daily, the Seattle-based drug company Sound Pharmaceuticals is set to soon begin a phase 2 clinical study for a

European Commission Approves Label Extension of Cystic Fibrosis Drug

According to a story from BioPortfolio, the biotechnology company Vertex Pharmaceuticals recently announced that the European Commission has approved a label extension for the company’s

What Can be Done to Resolve Shortages of Donated Organs for Transplant?

According to a story from The Chicago Tribune, insufficient supplies of donated organs that could be used for transplant surgeries result in 33 deaths per

MassBio President Knows Difficulty of Living with Cystic Fibrosis

According to the Boston Globe, the president of the Massachusetts Biotechnology Council has a personal stake in his continued advocacy for pharmaceutical development in his

New Updates From Translate Bio in Drug Development for Cystic Fibrosis and OTC Deficiency

According to a story from globenewswire.com, the messenger RNA therapeutics company Translate Bio recently released the latest updates in regards to two of its leading