Everlast talks about the difficulties with his daughter’s Cystic Fibrosis.
For more information, or if you would like to donate to The Cystic Fibrosis Foundation: https://www.cff.org/
Video Source
41 Comments
Leave a Reply
You must be logged in to post a comment.
My sons 9 he has cf there alot of medications involved.. I vs and it's scary. But he's healthy thank god he's getting on a medical trile .trifecta triple theropy .it's supposed to be a miracle drug. I hope everything works out for everyone with cf . Wee have to have faith in medical science.. Everlast is an inspiration to me and ever one involved in CF.xx
I hope Everlasts daughter has access to Trikafta. Life changing drug. We don’t have access in UK yet. If she’s double delta 508, she’ll be able to have it.
Both of my brothers have cystic fibrosis, yet I was the 1 in 4 not to get it.. the reason they didn't find it in a family history is because most of the time it was classed as pneumonia and the child died at an early age, rather than it being cystic fibrosis, look in family history for children that died to lung related illnesses early on up to the 1960.
My son has cystic fibrosis. He turned ten today. And u got necro thinking it's funny to diss cystic fibrosis. But a parent with a c.f child is a Soulja. Hope everlasts daughter is OK. It's really hard. There is lots of new meds.its a hard life but it's worth it. Hats of to u everlast .I just wish they can stable the condition. What is normal dude one love to everlast and his family stay strong bro
I have Cystic Fibrosis. I'm just as healthy as anyone else. I'm 17 years old, and have outlived all of my previous expiration dates.