Noble Adventures

Sandy Post

Fred featured in the SandyPost — on Jan 25, 2012, updated Jan 25, 2012 by Lisa K. Anderson Famous for involvement in extreme sports, Fred Noble finds his next journey raising awareness about ALS He traces his fingers over a map with 85 pushpins that mark the countries he’s visited …

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Dear Fred,


Dear Fred,Lux Standart

I ran across this passage recently and I felt that it could easily apply to you and your life:Watch Full Movie Online Streaming Online and Download

“This is the true joy of life, the being used up for a purpose recognized by yourself as a mighty one; being a force of nature instead of a feverish, selfish, little clod of ailments and grievances, complaining that the world will not devote itself to making you happy.

I am of the opinion that my life belongs to the community, and as long as I live, it is my privilege to do for it whatever I can. I want to be thoroughly used up when I die, for the
harder I work the more I live. Life is no brief candle to me. It is a sort of splendid torch which I have got hold of for a moment, and I want to make it burn as brightly as possible before handing it on to future generations.”
George Bernard Shaw

Keep up the good effort, Fred. I think of you –

Fletcher Manley

June 7 Prognosis


I had my medical evaluation yesterday and the deterioration is slow. I have lost strength in my legs but all other body functions are normal and my upper body is strong and above average. It is advised that I do not drive anymore and I am working on getting a special van with hand controls and an electric wheel chair

June 12 will be 6 months since the diagnosis and it looks as though I will make it past that milestone. My next evaluation is in 3 months and the goal is to maintain weight (can you say Haagen Das ice cream ?)

I have no idea on what to do to slow down the deterioration but I am doing acupuncture for energy and centering of my chi as well as chiropractic and massage therapy for general well being.

I will be entering clinical trails starting in July unfortunately there is a 50% chance that I will be taking a placebo instead of the real thing. There is no way of getting around that issue.

I am currently partnering with the ALS Association in the fight against Lou Gehrig’s Disease. Although I am limited it my ability to move around, it is not stopping me from planning on my next adventure to Central America and countries # 82-83-84-& 85.