Team Blazeman

Believe...Pick a stronger word than Hope...Cure.

blazedad
  • Male
  • Seekonk, MA
  • United States
Share on Facebook Share

Blazedad's Friends

  • James Nissen
  • Dany Seiler
  • Larry R. Harms
  • Milt MacFarlane
  • Andrea Lytle Peet
  • Simon Shurey
  • Korey Witt
  • Sean Luitjens
  • Just B
  • Rachel Mosier
  • David S. Leonard Sr.
  • Jordi Vidal
  • Ingrid Hartman
  • Barbara Sitter
  • Dave Tobin

blazedad's Groups

blazedad's Discussions

The -blazeman in a rarely seen note, his "reflections" on ALS and where he was in his life at that time!!!
1 Reply

Started this discussion. Last reply by blazedad Aug 19, 2017.

2006 Emmy Award...IMWC..."the-blazeman", (alswarriorpoet-spirit).

Started Apr 14, 2016

http://www.ironman.com/triathlon-news/articles/2007/05/ironman-celebrates-another-emmy-win.aspx#axzz2Fc5YoBm4
1 Reply

Started this discussion. Last reply by blazedad Apr 14, 2016.

Gifts Received

Gift

blazedad has not received any gifts yet

Give a Gift

 

Welcome,blazedad...jon's dad.

Latest Activity

blazedad left a comment for Alison Simmons
"Hi Bob, I hope all is well with you. I see (or at least I think I see) that you have set-up a new fundraising webpage through  http://teamblazeman.ning.com/. My Team Blazeman membership did not make the migration from the Active Giving website,…"
May 27
blazedad posted a status
"http://teamblazeman.ning.com/"
May 17
0 Comments
blazedad commented on blazedad's blog post “Expansion of the Blazeman ALS Tissue Collection.”
"Once again, this funding made it possible to attend the annual Neuroscience meeting where over 30,000 physicians and scientists from around the world meet to learn about recent advances in neuroscience research. We believe attendance at this meeting…"
May 2
blazedad commented on blazedad's blog post Rare Disease Day hosted by the Frank H. Netter M.D. School of Medicine at Quinnipiac University in Connecticut.
"Once again, this funding made it possible to attend the annual Neuroscience meeting where over 30,000 physicians and scientists from around the world meet to learn about recent advances in neuroscience research. We believe attendance at this meeting…"
May 2
blazedad's blog post was featured

Rare Disease Day hosted by the Frank H. Netter M.D. School of Medicine at Quinnipiac University in Connecticut.

Blazeman Warrior and medical student, Jenny Hansen and Shea Lawson from The Maryland Brain and Tissue Bank represented the Blazeman Foundation for ALS at this year’s Rare Disease Day hosted by the Frank H. Netter M.D. School of Medicine at Quinnipiac University in Connecticut.…See More
May 2
1 Comment
blazedad posted a blog post

Rare Disease Day hosted by the Frank H. Netter M.D. School of Medicine at Quinnipiac University in Connecticut.

Blazeman Warrior and medical student, Jenny Hansen and Shea Lawson from The Maryland Brain and Tissue Bank represented the Blazeman Foundation for ALS at this year’s Rare Disease Day hosted by the Frank H. Netter M.D. School of Medicine at Quinnipiac University in Connecticut.…See More
May 2
1 Comment
blazedad posted a status
"Remembering the -blazeman(alswarriorpoet-spirit)-Ironman's Braveheart-Today is the 14th anniversary of Jon's dx-so hard to believe-FREEDOM!"
May 2
0 Comments

Profile Information

Why did you become a Blazeman Warrior?
Jon Blais..."the -blazeman" is my son, it is our hope, his mother and I to work with every "Blazeman Warrior" to accomplish their goals while at the same time meet ours: raise awareness and funds for ALS research...in the War On ALS...to find a cure..."so others may live".
blazedad...jon's dad.

Despite 21 million(plus) people dying from ALS since 1869, there remains still no meaningful treatment or cure for this disease. Jon and ALS patients everywhere are basically offered the same treatment options as Lou Gehrig in 1939. Without raising awareness and funding, ALS will not receive the research efforts necessary to find a cure and will continue to strike down every person who is diagnosed with ALS...Join Jon, "fight the good fight"...Believe there will be a cure, and "others will live", bmom and bdad...jon's mom and dad.

blazedad's Photos

  • Add Photos
  • View All

blazedad's Videos

  • Add Videos
  • View All

Blazedad's Blog

Rare Disease Day hosted by the Frank H. Netter M.D. School of Medicine at Quinnipiac University in Connecticut.

Blazeman Warrior and medical student, Jenny Hansen and Shea Lawson from The Maryland Brain and Tissue Bank represented the Blazeman Foundation for ALS at this year’s Rare Disease Day hosted by the Frank H. Netter M.D. School of Medicine at Quinnipiac University in Connecticut.…

Continue

Posted on May 2, 2019 at 2:50pm — 1 Comment

Talk Story with Bob Babbitt...BabbittVille.

Talk Story with Bob Babbitt...Bob's insight into Jon, "the-blazeman's" story, (prior...during...post) IMWC-2005, Kona, HI.

                                   Talk Story...BLAZEMAN...March 1st, 2019...

Time for another edition of Talk Story with Bob Babbitt. I’m sharing some of my favorite stories that I’ve collected from my years in the wonderful world of endurance sports. This week I share the story of Jon Blais,…

Continue

Posted on March 1, 2019 at 5:30pm — 3 Comments

ALS Research update from Brandeis University...(ALS Research Labs).

Five years ago we created the Blazeman Post-Doc in the Rodal Lab at Brandies University. This collaboration resulted in many accomplishments. End of year 5 report and summary, overall achievements, and letters of thanks from Drs. Rodal and Deshpande.

Letter of Thanks from Dr. Rodal

Letter of Thanks from Blazeman PostDoc…

Continue

Posted on June 18, 2018 at 1:30pm — 1 Comment

Inspiring Age Groupers: The Legacy of Jon Blais..."the-blazeman", (alswarriorpoet-spirit).

https://www.facebook.com/IRONMANtri/videos/2012399588822561/UzpfSTEwOTM1NDE1MzU6MTAyMTY0MDE1NTg0MDY4ODc/…

Continue

Posted on May 13, 2018 at 1:30pm — 4 Comments

“Expansion of the Blazeman ALS Tissue Collection.”

Importance of ALS Tissue for Research

Posted on June 30, 2018 by blazeman

The University of Maryland Brain and Tissue Bank acknowledges the recent…

Continue

Posted on April 24, 2018 at 1:30pm — 11 Comments

Comment Wall (85 comments)

You need to be a member of Team Blazeman to add comments!

Join Team Blazeman

At 9:38am on September 17, 2014, Andrea Lytle Peet said…

Thanks, Bob!  We are putting together our plans and our team and should have some more teammates shortly :)  Keep fighting the great fight!

At 9:20pm on August 30, 2014, Andrea Lytle Peet said…

Thanks blazedad! I would definitely like to talk with you. I look forward to it - I will send you an email. You are in my thoughts as well, especially on Jon's birthday. You're right, we were meant to share.

At 11:51am on June 21, 2014, David S. Leonard Sr. said…

Thanks for the welcome blazedad...I will/my family will give everything I/we have "to fight the fight"..I will post race pictures of the Iron Horse Triathlon when its completed..6/29/2014...A close friend/assistant race director will be racing in Jon's honor(179)...thanks for accepting me into your family..

At 8:15am on October 14, 2013, blazedad said…
Robert Blais... If you will allow me to add a thought...it is really what Jon spoke to in 2006, something that he discovered as he raced his own races and participated with athletes in a sport that they and he loved...when racing for a "cau...se", whatever it was, the race was never defined by PR...DNF...for he knew, whatever the outcome...he could not have a bad race...something bigger than himself was the purpose...thus, in 2006 when he asked the multi-sport community to join him in his cause, (The WarOnALS)...he knew, and said, "maybe we can do something that the word would hear"...what we now define as the "Echo"...whatever is done in the cause, (ALS or???) an "Echo" is created...their voices are heard...Jon believed that we must "fight the good fight"...it must be with (strength, honor and commitment)...and that what we/you do, does "Echo" in eternity"...Gladiator...and that what has been started, must be finished...and, "others will live"...and so in the future we will hear those words never spoken, "I AM AN ALS SURVIVOR"...who knows, maybe at an IMWC...so, Freedom...(from ALS) and whatever your cause will be...G-D bless and thank you...bmom and bdad...for the -blazeman and the BF-ALS.
At 8:58am on August 15, 2013, blazedad said…

From Dan Dortic...
Bob,
"It has been and will always be my pleasure to help continue the
FIGHT. I don't know if you know this but that video is how I learned of Jon and
cannot watch it without feeling empowered while at the same time becoming
completely emotional. Those feelings is what Jon would have wanted athletes and
all people to feel. God Bless the BLAZEMAN for even in death he continues to
motivate, teach, and inspire."
FREEDOM!!
Dan

At 10:08am on August 7, 2013, blazedad said…

Summer Cycling for ALS During the month of August, why not dedicate every mile you ride to the War on ALS?  With help from our friends at Geared for Good, we've started a virtual fundraiser that makes it easy and fun to support the Blazeman Foundation with every pedal stroke.  Our goal: $5,000 by the end of August.  It's free to join, easily integrates with Garmin devices, and if you connect your social media feeds, your network of friends will be reminded each time you ride of your commitment to the cause.  Please join or donate at www.gearedforgood.com/BlazemanSummer.  As a way of saying thanks, every dollar you raise this month qualifies you to win a cycling jersey, courtesy of Geared for Good.  We hope you'll join the fight! Let's do some good this summer... So Others May Live.

Thank you for helping us in the WarOnALS...-blazeman and the Blazeman Foundation for ALS... Freedom...

At 8:28am on April 3, 2013, Diane Casselberry said…

Hello Blaze dad! I left you a message this morning. I have so many questions to ask you, and I'm so excited to join the team! I look forward to speaking with you soon so I can start fundraising :)

At 10:18am on April 2, 2013, Diane Casselberry said…

Thank you for your warm welcome! I am very interested in learning all I can about ALS and how to fundraise for it. My cousin Amy, has yet to tell her children about her diagnosis. While they see her difficulty walking and her parents moving in with them, the kids do not know the severity of the situation. I want to wait to being fundraising for her until she has told them. My plan is to do a little fundraising for both her and to fight ALS, how do I go about doing this? Would I have to do 2 separate fund raising pages, or can I designate like a 70/30 split? I'm really new to this whole thing, but I am committed to doing what I can to help. Thanks for all your help :)

Diane

At 5:02pm on November 12, 2012, John Maurice Hourihane said…

Thankyou Bob.

I sent a donation through the other site. I'll give Andrea a call in the morning.

 

Either way no worries. I look forward to seeing the water station at 3 and will plan drop and roll if I make the (when)  the line.

Thanks for taking the time to talk to me yesterday and today.

Mo

At 9:22am on July 30, 2012, Al Schlebecker said…

Thanks Blazedad! 

View All Comments

 
 
 

© 2019   Created by Joel Haugen.   Powered by

Badges  |  Report an Issue  |  Terms of Service

Sign in to chat!