#dpig

Kevin lobello was a huge minecraft fan and got his final dying wish granted to see the minecraft movie early. His mum and crew stories moved heaven and earth to make this happen before time ran out. He got to watch the movie in a private screening sat next to the boy who plays Henry in the movie, he also got a call from Jack black and jason mamoa before and after the film. He loved it and can be seen smiling though the movie. Sadly he passed away in his mother's arms on the 12th march just 11 days after getting his final wish fulfilled. He suffered from a rare and very aggressive form of brain cancer that presents in children called DIPG . He bravely fought the disease for 16 months .He is now at peace and up in heaven playing minecraft with technoblade and free from what the terrible disease did to his body. I no child cancer makes people feel uncomfortable and sad , but this disease desperately needs more funding to help find a cure. The federal government only gives four percent to research for child cancer and put of that 000.5 percent goes to dpig and now that funding has been cut to zero. Though federal funded drugs Kevin's mum was able to get 10 more months with him before this terrible disease took him . So please if you can go to the website chadtough.org and donate anything you can just type in kevin lobello and donate in his honor. Or type in to Google for kevin and read on his website how you can help and share his Story.

He was just 9 years old , it's nothing really is it he was still a baby . He had so much to live for and this cruel illness robbed him .

After finding this story I've got to admit I cried for two days. All I could think about was how I was sat there excitedly making holiday plans , while this little boy didn't even get to make it to ten . I researched this disease and read the horrible reality these poor babies go through. Thankfully now kevin is free from his failing body and no longer in pain , but there is thousands of kids out there still fighting and getting diagnosed with this every day . In my home county England 90 children every year get given this death sentence . Neil Armstrongs daughter died of this and there have been some advances but not alot, most children just red radiation and steroids which change them beyond recognition. All these children and families get is whats called a honeymoon period after theyve completed there radiation when stuff goes sort of back to normal so the family can cram everything the child wants to do before it comes back more aggressive, but some children dont even get that. Please please share this and Kevin's story around , his brave mum wants his story shared. Search using the term #forkevin and #digp

Sleep well little man your legacy will live on even though you are gone , through those that loved you and in your minecraft world you spent so much time in

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