Strollerderby

Dad Gives Away 500 Lobsters For Cystic Fibrosis Awareness

Posted by JeanneSager

I'm always amazed with the ways parents will fight for awareness for their kids' diseases. But I've got to give this Dad snaps (you'll forgive me for the bad nineties era reference in a moment). 

Don Hebert, a lobsterman from Marshfield, Mass., spent hours of his New Year's handing lobsters out for nothing - to spread the news about his seven-year-old son's fight with cystic fibrosis. 

There's no cure for the genetic condition which causes thickened mucus secretions, often putting a strain on CF sufferer's lung function. According to CysticFibrosis.com, the leading support site for CF patients, it's caused by "a genetic mutation that disrupts the cystic fibrosis transmembrane regulator (CFTR) protein."

Today's technology allows for CF to be caught via prenatal screenings - generally the chorionic villus sampling - but that's only if a mother has that particular test (it's not required in all states). Little Michael Hebert wasn't diagnosed until the day before he started kindergartent (he's now in first grade) after his coughing fits sent his parents to doctors looking for answers. At just seven, Michael has to put on a therapy vest twice a day to help loosen the mucus in his chest, and he makes frequent visits to Boston's Children's Hospital. Life expectancies for CF patients vary (the oldest known CF survivor lived to the ripe old age of seventy-six), but many succumb in their twenties or thirties.

For the Heberts, the idea was simply to let more people know it's out there. They weren't asking for money (hence the FREE lobsters, handed out long with pamphlets about cystic fibrosis). Don and his friends spent the latter part of the afternoon plowing driveways and shoveling steps and walkways, once again for free, to spread the word around town. 

In all, the Heberts handed out five hundred lobsters along with their pamphlets. I give Don snaps for creativity - and for being a good dad.

Image/Source: The Daily News Tribune

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+ DIGG + STUMBLE

Comments

 

BeausMom said:

Wow, what a great way to get the word out.  Kudos to this very special Dad. Thanks for blogging about this, people need to know how much this disease needs a cure.  We healthy people take breathing for granted, people with CF don't have that luxury for them each breathe is a struggle.

Thanks again.

January 5, 2009 10:49 AM
 

Melissa Smith said:

This is fantastic. Great food for a great cause! Kudos!

January 5, 2009 6:59 PM
 

Ashley said:

Thank you Jeanne for blogging about this fantastic dad. More people need to be aware of CF so we can find a cure.  

January 5, 2009 8:00 PM
 

Terri Yeisley said:

Great article, and wonderful story.  What a great dad!  As the grandmother of a 5yr old granddaughter w/cf--this touches my heart.  We need more people to know about this disease, as we have to raise our own money to fight for a cure.  Thank you for posting it!

January 5, 2009 8:33 PM
 

Scott Ose said:

Kudos to Don!! Well done and many thanks from the CF world! Happy New Year!

January 6, 2009 8:14 AM
 

Lily said:

Hi, this is Lily from the Cystic Fibrosis Foundation. Thanks for the post. This has to be one of the most unique ideas to raise awareness I have ever heard! Many thanks to Don for going above and beyond to help spread the word about CF. More information about CF and ways to get involved are on our Web site, www.cff.org if anyone is interested.

January 8, 2009 1:51 PM

About JeanneSager

Jeanne Sager is a writer who lives in upstate New York with her husband, daughter, a dog and too many cats. She refuses to believe motherhood comes with pumpkin appliqued sweaters, and she';s not ready to apologize for having only one child. She writes about raising her kid in her own hometown and the mom stuff she's not embarrassed to own at her blog, Inside Out (http://jeannesager.blogspot.com), she's contributing editor of Grand Magazine, and she's a regular essayist here on Babble

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