I have heard Cystic Fibrosis referred to as 'an invisible disease' meaning physically looking at someone with CF you may not know they had a terminal illness. That may be true at some point in a CFers life. . .but not entirely. The disease never felt 'invisible' to me when I looked at my barreled chest, clubbed fingers, port a cath, underweight body or when I gasped for air trying to recover from coughing. My CF became visible to everyone around me when I started wearing oxygen, became skin and bones, and lost the vibrant glow in my face. I literally got blue lips, blue fingertips and carried the expression of exhaustion. CF doesn't stay invisible forever.
If you don't know about Connor or his family. . . read this blog: Not So Bright and Shiny. Cystic Fibrosis is a nightmare. It's very real, it causes a lot of pain and it is taking Connor's life. He is just 7 years old. CF is not invisible!
I have heard that Connor's favorite color is RED. . .so here is a Red Rose for Connor.
*Please pray for Connor and his family that they will be comforted and find peace.*
Cystic Fibrosis needs a CURE. . . Cystic Fibrosis needs to be stopped!
Save a Life* Be Someone's Hero* Be an Organ Donor
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3 years ago
2 comments:
so true about the visiblity of this disease. Especially as it progresses. I find it funny that my size 4 waist requires a size 14 dress LOL...barrel chesting rocks!
Poor Conner and his family. It's such a sad sad story :(
My Father left a comment on a post regarding Connor on my FB page and I thought it was beautiful so I want to add it here~
"Some kids are too beautiful and priceless for this world. He probably endured a lifetime of pain, and now he'll have an eternity of joy." Doug Peery
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