Our Pulmonary Fibrosis Forums has been an incredible way to share resources with one another in the PF space. I recently came across another wonderful charity, working hard to help with IPF research, fund patient medical bills (through a grant process/application) and help raise awareness. If interested, please check out Hope for the Breath-Less charity.
I’ve had an opportunity this week to speak with Ruth, the founder of this charity and I am deeply touched by her efforts to fight this disease while also living with it!
How is PF Awareness month going for everyone?
What have you done/been able to do to help raise the profile of this cruel lung disease?
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