Hello! My Name is Melissa and I have a rare form of Albinism called hermansky pudlak syndrome. A symptom of this disease is Idiopathic Pulmanry Fibrosis, which has gradually decreased my lung function as well my ability to do the active things I love! Transplantation is my chance for more time here spent with my family and friends, as well as give me a chance to ride my bike again and get my black belt!
Family and friends of Melissa Webber are raising money for the nonprofit Help Hope Live to fund uninsured medical expenses associated with transplantation.
September 14, 2020
Currently waiting to be listed for Lung Transplant
Photo Galleries (1)
December 7, 2020
I pray for your speedy recovery.
I wish for Happy and Healthy Life.
God Bless you always
November 11, 2020
Wishing you all the best,
Don and Nancy O’Hara
September 16, 2020
To my good friend, Melissa. I'm hoping and praying for the best for you. I''ll be cheering you on thru your journey. I'm proud and inspired by your attitude of "Never give up and never surrender, except to the Lord Jesus Christ!" Your friend Bob Spayd.