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Have our post-transplant members heard about the rare and intriguing disease, Pulmonary Alveolar Proteinosis (PAP)?
In an amazing piece, fellow PH Columnist and transplant recipient Anna Jeter shares her journey, revealing the unbelievable transformation she feels just eight months after a provider’s discovery. You don’t want to miss her powerful column—link below!
Celebrating today’s victories to honor my younger selfHave you heard of another rare disease, potentially linked to transplant medications, called pulmonary alveolar proteinosis (PAP)? What are your thoughts on this inspirational story filled with gratitude?
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