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
Related posts:
- Episode 4 : All In The Family Often Awesome The Series is a web series about Tim...
- Episode 5 : Decoration Ghost – Part 1 Often Awesome The Series is a web series about Tim...
- Episode 7: Birds Of A Feather Often Awesome The Series is a web series about Tim...
- Episode 10 : Decoration Ghost Part 2 Often Awesome The Series is a web series about Tim...
- Episode 11 : True Love Episode 11 : True Love – This is the story...
Related posts brought to you by Yet Another Related Posts Plugin.
Subscribe to Something Awesome
Recent Comments
- Paul on Thanks to Savage Love podcast!
- admin on Update on Tim (from Lis Tyroler)
- Gary Guinn on Update on Tim (from Lis Tyroler)
- Matt on Update on Tim (from Lis Tyroler)
- Heidi van Deutsch on Update on Tim (from Lis Tyroler)
Contact Us
Resources
Blogroll
- ALS TDI
- ALS TDI Often Awesome Army
- Bright Side Of The Road
- Decoration Ghost
- Devender Sellars Design
- Ernest Jenning Record Co.
- Filthybird
- Help Ned Fight ALS
- Indestructable The Film
- Kudzu Wish
- Often Awesome Official Site
- Often Awesome The Series on Vimeo
- Often Awesome The Series on Youtube
- Prize 4 Life
- Rock Out ALS
- Snuzz
- Straight A Tattoo
- The Popovers
- Ties 4 ALS
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.
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.