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.
Episode 2 : “One Man’s Army” introduces us to the Often Awesome Army which is a group of Tim’s friends who put on benefit shows, art auctions and help raise money to provide for Tim’s quality of life care.
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: oftenawesomearmy.alscommunity.org
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February 26th, 2010 at 11:03 am
I remember the community that built up around my dad and mom when they were facing this. It made all the difference in the world. It was overwhelming and sometimes almost embarrassing to be the recipients of so much care and attention but it mostly made me understand how deeply we are all connected and how good peoples hearts really are. Thanks for sharing this story.
November 15th, 2011 at 5:42 pm
[…] Episode 2 (originally aired January 11, 2010) is entitled “One Man’s Army,” which begins with Kaylan and Tim talking about the days following Tim’s diagnosis. […]
April 16th, 2012 at 12:20 pm
I’d be happier if I could hear the people speaking over the music!
April 25th, 2012 at 9:10 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 16th, 2012 at 6:58 am
did this dude ever get tested for lyme disease?
November 16th, 2012 at 7:35 am
He got tested for everything. He has a genetic form of ALS which his mother and grandmother died from.
November 16th, 2012 at 7:38 am
he was one tough person to go through all this.
November 16th, 2012 at 10:42 pm
I read that many cases of ALS are just Lyme disease. Lyme disease is very hard to diagnose with most standard tests providing false negatives. Antibiotics reverse many peoples ALS apparently.
May 15th, 2013 at 4:59 pm
LOL That is the biggest load of crap I have ever heard. You must know NOTHING about ALS or Lymes disease.
July 7th, 2013 at 11:01 pm
This series is amazing, it helps appreciate every second I have with my aunt, who was diagnosed very late with ALS. Thank You for telling your story.
November 3rd, 2013 at 9:51 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.
May 29th, 2014 at 10:13 am
Lymes is what everybody wanted for me.I tested twice, 2nd was spinal fluid
even. I had a 104 temp in Jan there was 72 + hrs of 2 stronger
anti-biotics with IV. But in the end the same diagnosis ALS.6 months of
terror and torcher.
May 21st, 2015 at 3:54 pm
So beautiful, the power of love.