We left candles at Ibelin's grave in Elwynn today on Argent Dawn EU. It was a very sweet gathering.
Glad Netflix does know the EU exists opposed to Blizzard. Even German Translation is available :)
Finally! I've wanted to see this for a long time. The story sounds very powerful on its own. Still, even though I don't have any serious disabilities or was in the same situation as Ibelin, I think it'll resonate on an even deeper level as I can relate to using WoW RP as a very much-needed escape during a specific period of my life. This isn't a widely covered subject or anything I talk to people about, so while this powerful story is and will always belong to Ibelin, I'm grateful for it.
that's a W.
Anyone knows the cordinates for the gravestone?
I was on Netflix earlier n ran into this, wasn't gonna watch cause I'm not one for documentaries type movies but decided to check it out, I'll admit I didn't know what I was getting into but the fact RP can connect folks like that is amazing, in all my 19yrs of WoW raiding I met a lot of ppl n this documentary made me wonder about those ppl I met n hope if they are still here that they're living a wonderful life.
It's depressing AF that Argent Dawn EU is now a cesspool of toxic personalities that will bully you into an early grave
I'm so glad Ibelin's parents learned he lived this life with his community. The documentary made us sob throughout. Now, he will be forever remembered in-game.
Reckful briefly appears in the frame when Ibelin pops his head out of the water. Nice touch by the animators, and fantastic documentary.
F
whole trailer is in englishturn on movie: NORWEGIAN
Damn he died during WoD that really really sucks
I highly recommend watching this if you can. Great story.... told well using Mats own words.
Fantastic docu and nice to see how games like WoW can bring people together and create something so positive. We need this in bad times like these. Spread kindness and love <3
Very sad. My wife and I got the diagnosis 2 years ago that my son (now 4) has DMD. It's a terrible disease the progresses over time. We fought to get him into a Gene therapy trial with Pfizer and was one of 10 kids his age that got accepted after many tests/immunology tests. He went from not walking to walking in 2 weeks after the gene therapy infusion. It is not a cure and too soon to see it's true progress, but anything at this point is a plus. This disease is more prevalent in boys and can be passed through the mother. We got my wife tested and she was not a carrier so it was just a random mutation for my son. Prays for everyone with DMD and their families.