Often Awesome The Series is a web series about Tim and Kaylan’s battle with ALS. It’s a story about love, friends, strength and courage. Join us every two weeks for a new chapter in this amazing adventure.
For more information about Tim and Kaylan’s fight visit : oftenawesome.org
If you are interested in funding research, please make tax deductible donations to the ALS TDI at: als.net
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December 28th, 2009 at 4:17 pm
[...] This post was mentioned on Twitter by Anthony Sanders, Brandon Sexton. Brandon Sexton said: Please check this out. Tell your friends too. http://bit.ly/4J2zcD [...]
January 4th, 2010 at 8:09 am
I am so moved by the love and support you have for one another. Please continue and good luck.
January 31st, 2010 at 11:44 pm
[..YouTube..] Does medical cannabis work for ALS? Haven’t heard much about that like MS but you never know…
January 31st, 2010 at 11:44 pm
[..YouTube..] Does medical cannabis work for ALS? Haven’t heard much about that like MS but you never know…
January 31st, 2010 at 11:44 pm
[..YouTube..] Does medical cannabis work for ALS? Haven’t heard much about that like MS but you never know…
January 31st, 2010 at 11:44 pm
[..YouTube..] Does medical cannabis work for ALS? Haven’t heard much about that like MS but you never know…
January 31st, 2010 at 11:44 pm
[..YouTube..] Does medical cannabis work for ALS? Haven’t heard much about that like MS but you never know…
January 31st, 2010 at 11:44 pm
[..YouTube..] Does medical cannabis work for ALS? Haven’t heard much about that like MS but you never know…
January 31st, 2010 at 11:44 pm
[..YouTube..] Does medical cannabis work for ALS? Haven’t heard much about that like MS but you never know…
January 31st, 2010 at 11:44 pm
[..YouTube..] Does medical cannabis work for ALS? Haven’t heard much about that like MS but you never know…
January 31st, 2010 at 11:44 pm
[..YouTube..] Does medical cannabis work for ALS? Haven’t heard much about that like MS but you never know…
January 31st, 2010 at 11:44 pm
[..YouTube..] Does medical cannabis work for ALS? Haven’t heard much about that like MS but you never know…
January 31st, 2010 at 11:44 pm
[..YouTube..] Does medical cannabis work for ALS? Haven’t heard much about that like MS but you never know…
January 31st, 2010 at 11:44 pm
[..YouTube..] Does medical cannabis work for ALS? Haven’t heard much about that like MS but you never know…
January 31st, 2010 at 11:44 pm
[..YouTube..] Does medical cannabis work for ALS? Haven’t heard much about that like MS but you never know…
January 31st, 2010 at 11:44 pm
[..YouTube..] Does medical cannabis work for ALS? Haven’t heard much about that like MS but you never know…
January 31st, 2010 at 11:44 pm
[..YouTube..] Does medical cannabis work for ALS? Haven’t heard much about that like MS but you never know…
January 31st, 2010 at 11:44 pm
[..YouTube..] Does medical cannabis work for ALS? Haven’t heard much about that like MS but you never know…
January 31st, 2010 at 11:44 pm
[..YouTube..] Does medical cannabis work for ALS? Haven’t heard much about that like MS but you never know…
January 31st, 2010 at 11:44 pm
[..YouTube..] Does medical cannabis work for ALS? Haven’t heard much about that like MS but you never know…
March 17th, 2010 at 11:52 am
I too have been diagnosed with ALS and my mother died from it in 1988. I have AFO’s on both feet. I am retired from teaching but continue to substitute and teach adults in hopes that the will get their GED. Good luck to you. Lets hope and pray for a cure.
March 21st, 2010 at 3:10 am
I also have ALS but not the familial variety and I am an old fart with a life well lived and really nor reason to hang around for long. I have been following this series on Facebook but tonight is the first time I sat down and watched all the videos. You are doing us all such a great service, and I am so grateful for your willingness to share your life with this disease from the very start. I wish you well, both Tim and Kaylan, because not one of has the disease alone. It is a family or partnership disease. Your support system speaks volumes of your worth, a worth that far exceeds your age.
September 15th, 2010 at 2:40 pm
[..YouTube..] @MikeCANN not usually as the best benefits are usually via smoking for most illnesses-this is more likened to cerebral palsy&needs intense hands on work all day. Narcs have IM&IV&12-24hr forms. Swallowing gets difficult and patches are only now in development for canabis. It’s only legal in a handful of states as is.
September 15th, 2010 at 2:40 pm
[..YouTube..] @MikeCANN not usually as the best benefits are usually via smoking for most illnesses-this is more likened to cerebral palsy&needs intense hands on work all day. Narcs have IM&IV&12-24hr forms. Swallowing gets difficult and patches are only now in development for canabis. It’s only legal in a handful of states as is.
September 15th, 2010 at 2:43 pm
[..YouTube..] Thanks Blake&co for doing this. Are you guys partners? It could help once this gets the views it really should. I don’t know all the details of partnering but you guys should definitely consider it. DoC could profit from the full film on here should you ever become a partner. My prayers are with Tim and his awesome team. The Project for Awesome-ALL about awareness&raising $-NEEDS to have this story. Ask Hank Green of the Vlogbrothers for more info.
March 29th, 2011 at 6:34 am
[..YouTube..] I just met Andy Coon at the LA Web Fest. Wow, I had no idea! What an interesting story.
March 29th, 2011 at 6:34 am
[..YouTube..] I just met Andy Coon at the LA Web Fest. Wow, I had no idea! What an interesting story.
March 29th, 2011 at 6:34 am
[..YouTube..] I just met Andy Coon at the LA Web Fest. Wow, I had no idea! What an interesting story.
March 29th, 2011 at 6:34 am
[..YouTube..] I just met Andy Coon at the LA Web Fest. Wow, I had no idea! What an interesting story.
March 29th, 2011 at 6:34 am
[..YouTube..] I just met Andy Coon at the LA Web Fest. Wow, I had no idea! What an interesting story.
March 29th, 2011 at 6:34 am
[..YouTube..] I just met Andy Coon at the LA Web Fest. Wow, I had no idea! What an interesting story.
March 29th, 2011 at 6:34 am
[..YouTube..] I just met Andy Coon at the LA Web Fest. Wow, I had no idea! What an interesting story.
March 29th, 2011 at 6:34 am
[..YouTube..] I just met Andy Coon at the LA Web Fest. Wow, I had no idea! What an interesting story.
March 29th, 2011 at 6:34 am
[..YouTube..] I just met Andy Coon at the LA Web Fest. Wow, I had no idea! What an interesting story.
March 29th, 2011 at 6:34 am
[..YouTube..] I just met Andy Coon at the LA Web Fest. Wow, I had no idea! What an interesting story.
March 29th, 2011 at 7:08 pm
[..YouTube..] @tanjareen Thanks, Tanjareen. It was great meeting you at the LA Web Fest. Looking forward to watching your series.
March 29th, 2011 at 7:08 pm
[..YouTube..] @tanjareen Thanks, Tanjareen. It was great meeting you at the LA Web Fest. Looking forward to watching your series.
March 29th, 2011 at 7:08 pm
[..YouTube..] @tanjareen Thanks, Tanjareen. It was great meeting you at the LA Web Fest. Looking forward to watching your series.
March 29th, 2011 at 7:08 pm
[..YouTube..] @tanjareen Thanks, Tanjareen. It was great meeting you at the LA Web Fest. Looking forward to watching your series.
March 29th, 2011 at 7:08 pm
[..YouTube..] @tanjareen Thanks, Tanjareen. It was great meeting you at the LA Web Fest. Looking forward to watching your series.
March 29th, 2011 at 7:08 pm
[..YouTube..] @tanjareen Thanks, Tanjareen. It was great meeting you at the LA Web Fest. Looking forward to watching your series.
August 31st, 2011 at 4:31 am
I just came across this story from the blog “pacing the panic room” I really want to know more and would love to watch the series from the beginning but I am unable to get any of the first videos to load. Help, please
January 11th, 2012 at 11:12 pm
[..YouTube..] RIP. What a brave man to go through all of that. I hope we can do something about this disease soon.
January 12th, 2012 at 4:43 pm
[..YouTube..] Thank you for sharing this series! I’m so happy to see people trying to raise awareness for ALS and this man is inspiring, not only to people as a majority, but to other young (and old) people like me who do have this disease. I’m sorry he is not here in body any more, but I hope his family take pride and comfort he is here in spirit and a great help to others, even though he’s gone. Bless the people making this series and the family willing to share their story! I hope we can find a cure soon!!