The Lactose Intolerance Clearinghouse Has Moved.

My old website can be found at I am no longer updating the site, so there will be dead links. The static information provided by me is still sound.

For quick offline reference, you can purchase Planet Lactose: The Best of the Blog as an ebook on or or or a whole lot of other places that Smashwords is suppose to distribute the book to. Almost 100,000 words on LI, allergies, milk products, milk-free products, and the genetics of intolerance, along with large helpings of the weirdness that is the Net.

I suffer the universal malady of spam and adbots, so I moderate comments here. That may mean you'll see a long lag before I remember to check the site and approve them. Despite the gap, you'll always get your say. I read every single one, and every legitimate one gets posted.

Sunday, September 23, 2007

Sarah's Cure

I've written about Galactosemia before.

People with galactosemia digest lactose properly, splitting it into the simple sugars glucose and galactose, but they lack the enzyme that converts the galactose into more glucose. The galactose accumulates in the bloodstream and effectively poisons the body. This otherwise completely harmless sugar can lead to brain damage, blindness and death through liver failure. Only one in 80,000 babies are born with this condition.

Sarah Southard of Texas is another little girl with this lifelong problem. Because it is so rare, there has been little research and no possibility of a cure in sight. Her family wants to change that.

An article by Jessica Langdon in the Wichita Falls TimesRecordNews reports that for the second year they're staging a fundraiser called "Sarah's Cure."

For the second year in a row, the Southards are inviting the North Texas community to help Sarah — and all children who have Galactosemia — during an October Saturday filled with fun and Texas music in Decatur.

The event is called “Sarah’s Cure,” and this year, it’s a project of a group the Southards spearheaded — a nonprofit organization called Galactosemic Families of the Southern States. Funds will go to the national group, Parents of Galactosemic Children Inc., to help fuel research.

For more information:

Parents of Galactosemic Children Inc.
Parents of Galactosemic Children, Inc. (PGC) is a national, non-profit, volunteer organization whose mission is to provide information, support, and networking opportunities to families affected by galactosemia.

Galactosemic Families of the Southern States.
Galactosemic Families of the Southern States is a non-profit, volunteer organization that was created by parents just like you. We are a support system for families in Texas, Oklahoma, Arkansas and Louisiana who live with galactosemia everyday.

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1 comment:

Mark Southard said...

Hi, my name is Mark Southard, the dad of Sarah Southard. It is my wife, Jo Beth, and I that organized the 2nd annual "Sarah's Cure" benefit concert. It was really great to see the very useful and accurate information you put out regarding Galactosemia. We were also involved in starting our local support group "Galactosemic Families of the Southern States". Thanks for what you do, gaining awareness in the general public is one of the keys to finding a cure!