Team AlecGators Takin' a Bite Out of Duchenne

Team AlecGators Takin' a Bite Out of Duchenne We run because we can. We run because others can not. We run because we want a cure! He no longer walks, as bad as that sounds, Mom, Dad & Alec are relieved.

Alec is considered stable for an almost 12 year old with Duchenne Muscular Dystrophy (DMD). Mom and Dad were always scared that the next fall was going to result in a break, and just didn’t trust himself. Now that he has a power chair – he has all the confidence in the world. His heart is starting to show signs of disease and his arms are growing weaker. Currently with updated medicine for his hea

rt and increase in dosage to slow down the progression of DMD – Alec is able to play the Xbox all day (if Mom would just let him). DMD has taken is ability to walk, but not his wit. For the last year, he has been tooling around school and our neighborhood in his power wheelchair. Alec has been spotted being a typical boy with his wheels either pulling buddies around the icy driveway on a sled or treating his sister and a friend to an electronic marry-go-around. Last fall, he participated in the first season of the Miracle League. And just a few weeks ago he became a Boy Scout and he is looking forward to shooting bb guns, firearm and knife safety, leather working, and wood carving. Alec has made himself a goal to be an Eagle Scout.

In 2 weeks Matt and Trisha will run the Chicago marathon for all boys with Duchenne. They’re still short on their fundra...
09/25/2022

In 2 weeks Matt and Trisha will run the Chicago marathon for all boys with Duchenne. They’re still short on their fundraising. Can you help them reach their goals and in turn help find a cure for DMD?

Support AlecGators as we take a bite out of Duchenne!!!

02/09/2022

Trisha and I are running the Chicago marathon together this fall to raise money and awareness for Duchenne. Please support our run or join our team.

08/17/2019

Good luck to Team AlecGators at Mitchell’s run today!!!!

I remember August of 2009 when Janell Lundy called to inform me of this group called Run For Our Sons. Since that phone ...
10/19/2018

I remember August of 2009 when Janell Lundy called to inform me of this group called Run For Our Sons. Since that phone call I have ran 370.4 race miles 4 of us will run 13.1 more on Sunday morning and Trisha & I will run 26.2 miles in January. Since that day Team AlecGators have raised $51,424.96, how high can we make that total raise by the time Maureen, Hillary, Ennessa Trisha & I's bibs cross the finish line of the GR 1/2 marathon on Sunday?

http://join.parentprojectmd.org/site/TR/raceevent/General?team_id=13298&pg=team&fr_id=4932

Watch this video to see this is why we will run 26-48 miles. Please help us achieve our goal. Click here to donate: http...
12/08/2017

Watch this video to see this is why we will run 26-48 miles. Please help us achieve our goal.
Click here to donate: http://www.parentprojectmd.org/site/TR/Events/General…

Duchenne is a fatal genetic disorder diagnosed in early childhood that slowly robs young men of their muscle strength. Help us go the distance to end Duchenn...

This year in addition to running the 48.6 mile D***y Challenge my wonderful girlfriend Trisha Diane Law-Crotser will joi...
09/27/2017

This year in addition to running the 48.6 mile D***y Challenge my wonderful girlfriend Trisha Diane Law-Crotser will join me for the 13.1 mile half marathon. We are raising money for Duchenne Muscular Dystrophy so one day Alec Lundy and other boys can be just another boy. Every dollar gets us one step closer to a cure.

We're joining together to raise funds and awareness to support Parent Project Mucsular Dystrophy's fight to end Duchenne, a progressive, fatal muscle disorder for which there is no cure.

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9177 Shady Lane
Lakeside, MI
49116

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