Often Awesome The Series is a web series about Tim and Kaylans battle with ALS. Its a story about love, friends, strength and courage. Join us every two weeks for a new chapter in this amazing adventure.
Episode 6 : “Friends With Benefits” Not long after learning of his diagnosis, Tim’s friends organized a benefit show to help raise money for his quality of life care and to create awareness about ALS.
For more information about Tim and Kaylans fight visit : oftenawesome.org
If you are interested in funding research, please make tax deductible donations to the ALS TDI at: oftenawesomearmy.alscommunity.org
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March 8th, 2010 at 2:14 pm
Thanks for sharing! I really enjoy your story. Keep up the good work!
March 8th, 2010 at 3:38 pm
Thanks for viewing and please help to spread the word.
March 8th, 2010 at 6:42 pm
This series has been moving, funny, and very informative, especially being so far away. I’m so proud of all the folks i see working to help Tim and Kaylan. Y’all look so grown up on the video!
March 8th, 2010 at 9:01 pm
This episode was the best yet. You guys are all doing such a great job. Keep it up!!
March 8th, 2010 at 10:43 pm
Thanks Rosa. Help spread the word.
March 14th, 2010 at 8:09 am
Love the title.
March 14th, 2010 at 8:10 am
Love the title.
March 14th, 2010 at 9:21 am
[..YouTube..] Lovely. Crying with happiness.
October 25th, 2010 at 3:52 pm
For one old man whose life is behind him and one who is on the same journey as Tim this video series is one of the most effective tools for awareness I have seen. I peeked ahead at some of the latest videos and am struck with the brave portrayal of this disease and its progression that Tim and his army has documented. I say bravo for a super project.
January 13th, 2012 at 6:43 am
my heart goes out to ya all…reminds me of my hippy days when we all helped one another get through problems
April 25th, 2012 at 9:06 am
The series is nominated for Best Documentary Series for a Webby. Please help us take home the People’s Voice Award for voting! Go to the youtube titled: “Often Awesome The Series: An ALS Love Story Official Trailer”, and click the link to the Webby awards. Ends 4/26/2012.
November 3rd, 2013 at 9:53 pm
My name is Helen Barratt and my mother died of MND or Lou Gehrig’s ALS in 2009. My latest forum article called ‘Australian Researchers Discover Potential Blue Green Algae Cause & Treatment of Motor Neuron Disease (MND)&(ALS)’ and its link to Parkinsons’s and Alzheimer’s diseases can be found at Science20 under the medicine forum.